Less Chronic Pain After Lichtenstein Hernioplasty Using the Self-gripping Parietex Progrip Mesh (HIPPO)
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|ClinicalTrials.gov Identifier: NCT01830452|
Recruitment Status : Unknown
Verified April 2013 by Marijke Molegraaf, Groene Hart Ziekenhuis.
Recruitment status was: Recruiting
First Posted : April 12, 2013
Last Update Posted : April 12, 2013
|First Submitted Date ICMJE||February 6, 2013|
|First Posted Date ICMJE||April 12, 2013|
|Last Update Posted Date||April 12, 2013|
|Start Date ICMJE||September 2010|
|Estimated Primary Completion Date||March 2015 (Final data collection date for primary outcome measure)|
|Current Primary Outcome Measures ICMJE
||Incidence of chronic post-operative inguinal pain [ Time Frame: 12 months ]
The definition of chronic pain given by the IASP will be used.
|Original Primary Outcome Measures ICMJE||Same as current|
|Change History||No Changes Posted|
|Current Secondary Outcome Measures ICMJE
||Recurrence rate [ Time Frame: 12 months ]|
|Original Secondary Outcome Measures ICMJE||Same as current|
|Current Other Outcome Measures ICMJE
|Original Other Outcome Measures ICMJE||Same as current|
|Brief Title ICMJE||Less Chronic Pain After Lichtenstein Hernioplasty Using the Self-gripping Parietex Progrip Mesh|
|Official Title ICMJE||Multicentre Randomised Controled Trial Comparing the Effect of a New Self-gripping Lightweight Polyester Mesh and a Normal Sutured Lightweight Polyester Mesh on the Incidence of Chronic Inguinodynia in Lichtenstein Hernioplasty.|
Chronic pain after Lichtenstein hernioplasty is a common problem with an incidence of 11%. Many factors influence the onset and persistence of pain. Mesh characteristics and fixation have been pointed as important etiologic factors. This study compares two types of fixation for the same mesh. The mesh used is a lightweight parietex mesh. In the control group this mesh will be fixed with non absorbable sutures. In the study group sutures will not be needed because of self gripping microhooks on the surface of the mesh.
Methods: The HIPPO trial is a multicenter double blind randomized clinical trial. Patients will be randomly allocated to the sutured mesh or the self-gripping mesh. Hernia repair will be done according to Lichtenstein as described by Amid et all. Included will be all unilateral primary inguinal hernia in man patients aged 18 years or older not meeting the exclusion criteria. Patients will be followed for two years. The main endpoint is the amount of post-operative chronic pain evaluated by VAS scores. The existence of neuropathic pain will be evaluated by the Paindetect questionnaire (and a bedside variant of the QST). Secondary endpoints are recurrence rate, post-operative complications, costs, hospital stay, QOL, return to work and daily activities, genital and sexual problems. To demonstrate a difference in VAS score of 10 with α=0.05 and power 80% a sample size of 400 patients is calculated.
Discussion: Hypothesized is that the self gripping non-sutured mesh (Parietex Progrip) will cause less post-operative and chronic pain without enhancing the recurrence rate.
In 1984 Lichtenstein popularized routine use of a heavy weight polypropylene mesh fixed with non-absorbable sutures to create a tension-free hernioplasty. This technique became the gold standard in many clinics due to its low rate of recurrence and direct post-operative pain6. Focus has now shifted to the occurrence of chronic pain and neuralgia after Lichtenstein hernioplasty. Chronic post-operative pain has been defined as pain lasting more than 3 months after surgery. The surgical repair technique seems to be an important etiologic factor in this. This includes aspects like type of mesh used, manner of fixation of the prosthetic material and handling of the cutaneous nerves.
The aim of this study is to investigate differences in incidence of chronic post-operative pain between the two types of fixation for the same mesh. The mesh used is ligthweight and made of polyester. The mesh will be fixated by either non-adsorbable sutures, according to Lichtenstein, or by small microhooks on the lower surface of the mesh (Parietex Progrip Mesh, Covidien).
Rationale for the Parietex Progrip Mesh
To reduce post-operative chronic pain it is thought being important to use low weight large pore size oligofilament meshes fixed with a minimal use of devices or no devices at all. This both to minimize compression/entrapment neuropathy and inflammation. The Parietex Progrip mesh biocompatibility is enhanced using low-weight monofilament isoelastic polyester with large pores. The hydrophilic characteristics of polyester are known to cause less shrinkage and fibrotic tissue formation than the more standard polypropylene.
The need for fixating devices is bypassed by small absorbable microhooks (polyactid acid, PLA) on the surface of the Progrip Mesh. Mesh fixation by the micro hooks to the underlying groin tissue is achieved instantly after exerting light pressure on the mesh. The fixation by the micro-hooks is achieved for the fully mesh area in contrast to other meshes in which only the margins of the mesh are sutured. Therefore it is likely that there is less risk of movement or displacement of the hernial sac under the mesh. The PLA micro hooks will be completely resorbed after 15 months. Then the mesh is firmly connected to the groin bed by tissue ingrow. After resorption of the PLA only the low-weight (38 g/m2) monofilament polyester (PP) will be left in situ.
The mesh has an oval shape with a self-gripping flap to be placed around the spermatic cord at the internal ring.
A recently performed pilotstudy comparing the Parietene (made of polypropylene) Progrip mesh to the standard mesh in the clinic, a heavy weight sutured polypropylene mesh, revealed a significant lower incidence of chronic pain in the Parietene Progrip group (P=0.012). Recurrence rates were not different. Operation time was significantly shorter for the Parietene Progrip Mesh group.(p=0.002).
The aim is to compare two types of fixation for the same mesh in inguinal hernia repair as described by Lichtenstein; a lightweight polyester mesh which has to be sutured will be compared to a lightweight polyester mesh with self-gripping properties not needing any fixating devices. It is already proved that lightweight meshes reduce the amount of foreign body reaction resulting in less chronic pain. The self fixing properties are believed to enhance this effect by minimizing entrapment of muscle and nerve fibres.
The primary endpoint is the amount of post-operative chronic groin pain. This will be evaluated using visual analogue scale (VAS) and Mc Gill Pain questionnaire. In a subgroup of 50 patients the amount of pain en pain threshold before and after the hernioplasty will be objectified by quantitative sensory testing (QST).
Secondary objectives are recurrence rate, per operative and post-operative complications, operating time, duration of hospital stay, costs, return to work and daily activities, QOL, genital and sexual problems.
The HIPPO trial is a multicenter double blind randomized clinical trial. Preoperative randomization will be done using an official randomisation program. All included study subjects will be registered in this program. On the day of surgery the operation assistant will login in the randomisation program and start the randomisation procedure for the patient to be operated. The outcome will appear in a couple of seconds and will be stored in a secured database. Which type of mesh is to be used will be known for the surgeon not earlier than preparation of the inguinal floor is finished and the surgeon is ready to place a mesh. In the case the patient is not sleeping during the operation it is possible that he notice whether the mesh is fixed with sutures or not. To be sure this will not happen patients who do not want to sleep will get an ear-radio and eye mask.
The investigator assessing the outcome on the outpatient department will not be informed about the outcome of randomisation. Besides this, operation reports will not mention which type of mesh has been used. The randomisation code can be broken by the owner of the randomisation program, but only in case of a medical urgency and in order of a medical doctor.
Patients will be included on the outpatient clinic of the department of General Surgery of the departing hospitals. This will be done by surgeons and supervised residents. After inclusion patients have to sign informant consent and fill in a couple of questionnaires: SF36 (Short Form, measuring quality of life), McGill pain questionnaire, VAS, Dutch and Inguinal hernia questionnaire (to be validated). Follow-up will be at 2weeks, 3 months, 12 months and 24 months post-operatively. For each follow-up visit patients have to complete the same questionnaires at home. Besides this they will be examined on the clinic for the detection of complications (eg recurrence, wound problems) and to perform sensibility tests.
Subjects can leave the study at any time for any reason if they wish to do so without any consequences. The investigator can decide to withdraw a subject from the study for urgent medical reasons
Sample size calculation
The primary endpoint is the VAS score. A difference of 10 in post-operative Visual Analogue Scale score between the intervention and control group is considered to be the minimum relevant clinical difference. According to the power analyse, 169 patients per treatment group are needed to achieve this with a power of 80% with an alpha of 5%. The calculation was made with a two-sided test for the VAS pain score at 3 months. Based on the pilotstudie the standard deviation was set at 20.
Statistical comparison will be made using the Wilcoxon test for continuous data and the Pearson chi squared test for ordinal data. The Wilcoxon test will also be used to analyse the SF36 scores and nominal operative parameters. P<0.05 will be considered statistically significant.
Ethics, informed consent
The study will be conducted according to the principles of the Declaration of Helsinki 59th amended by the World Medical Association General Assembly, Seoul, October and in accordance with the Medical Research Involving Human Subjects Act (WMO). The protocol has been approved by the independent ethics committee of the participating hospitals and the Leiden University Medical Centre. All patients who are asked to co-operate in the study are verbally informed and by patient information letter. The handling of personal date will comply with the Dutch Personal Data Protection Act. Data will be saved for maximal 5 year after public disclosure of the research results.
An inguinal hernia is defined as a protrusion of the contents of the abdominal cavity or preperitoneal fat through a hernia defect in the inguinal area which can be congenital or acquired. This situation can give rise to complaints such as discomfort and pain. Conform the recommendation of the EHS (European Hernia Society, last version 2009) the diagnosis of inguinal hernia will be established by means of physical examination. Groin diagnostic investigations will be performed only in patients with obscure pain and/or swelling. The inguinal hernia will be classified using the EHS classification.
Pre-operatively all patients will be seen by the anaesthetist on the pre-operative outpatient clinic. The type of anaesthesia (general or spinal with short acting agents) will be decided by the anaesthetist taking into account the preference of the patient. There are standard protocols for the general or spinal anaesthesia.
The inguinal hernia will be corrected according to Lichtenstein, as described by Amid et all. This is the treatment recommended for primary unilateral inguinal hernia by the Dutch Society of Surgeons and the European Hernia Society. In half of the study population a lightweigth polyester mesh (Parietex Mesh, Covidien) will be used, fixed with non-absorbable sutures as described by Amid. In the other half a lightweigth self gripping polyester mesh (Parietex Progrip Mesh, Covidien) will be used. This mesh will be placed the same way as the sutured mesh e.g. tension free over the posterior wall of the inguinal canal 1cm overlapping the pubic bone and inguinal ligament. The self gripping flap will be closed loosely around the spermatic cord. Fixation will be achieved by applying light pressure on the mesh. No fixating suture(s) are necessary. The parietex progrip mesh is preshaped, but corrections in size are allowed to be made.
Conform the recommendations of the EHS the inguinal nerves at risk (ilio-inguinal, iliohypogastric and genitofemoral nerve) will be tried to be identified, because this may reduce the risk of nerve damage and post-operative groin pain. In principle the nerves will be preserved, but in case of damage or interference with the mesh they will be resected.
It is recommended that, in the case of large hernia sac, transection of the hernia sac is performed and the distal hernia sac is left undisturbed, so as to prevent ischaemic orchitis. If necessary, a large direct hernia will be sutured tension-free with continuous soluble sutures until a flat posterior wall has been created with a normal internal ring. Operations will be performed by surgeons or supervised residents.
Post-operative pain control and recovery
After hernia repair the wound will be locally infiltrated with analgesics to provide extra pain control and limit the use of analgesics. The amount of painkillers given to the patients will depend on their VAS score. This is a standardised regimen based on current practice. Post-operative painkillers include paracetamol 1 gram four times daily and diclofenac 50 gram three times daily. When this is not satisfying tramadol 50mg 3 times daily can be given. According to the EHS there are no limitations placed on patients following inguinal hernia operation and patients are, therefore, free to resume activities. They are only advised to limit heavy weight lifting for 2-3 weeks after surgery.
The HIPPO is a double blind randomised controlled trial that aims to show a reduction in chronic pain after anterior inguinal hernia repair with placement of a self gripping Parietex Progrip Mesh compared to the same mesh but sutured according to Lichtenstein. Hypothetically the Parietex Progrip Mesh reduces chronic pain compared to Lichtenstein because of less harm to underlying nerve and muscle fibers.
Competing interests The authors declare that they have no competing interests. Objective analyses will be performed on the TULIP data. There will be no violating of this study protocol.
|Study Type ICMJE||Interventional|
|Study Phase||Phase 4|
|Study Design ICMJE||Allocation: Randomized
Intervention Model: Factorial Assignment
Masking: Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
|Intervention ICMJE||Procedure: Self-fixating Parietex Progrip Mesh
Lichtenstein hernioplasty using a self fixating Parietex Progrip mesh not needing any fixating devices
|Publications *||Not Provided|
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
|Recruitment Status ICMJE||Unknown status|
|Estimated Enrollment ICMJE||400|
|Estimated Completion Date||March 2015|
|Estimated Primary Completion Date||March 2015 (Final data collection date for primary outcome measure)|
|Eligibility Criteria ICMJE||
|Ages||18 Years and older (Adult, Senior)|
|Accepts Healthy Volunteers||No|
|Contacts ICMJE||Contact information is only displayed when the study is recruiting subjects|
|Listed Location Countries ICMJE||Netherlands|
|Removed Location Countries|
|NCT Number ICMJE||NCT01830452|
|Other Study ID Numbers ICMJE||NL27506.058.09|
|Has Data Monitoring Committee||No|
|U.S. FDA-regulated Product||Not Provided|
|IPD Sharing Statement||Not Provided|
|Responsible Party||Marijke Molegraaf, Groene Hart Ziekenhuis|
|Study Sponsor ICMJE||Groene Hart Ziekenhuis|
|Collaborators ICMJE||Erasmus Medical Center|
|PRS Account||Groene Hart Ziekenhuis|
|Verification Date||April 2013|
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