Prophylactic Endoscopic Clipping of Diverticula (PECoD) (PECoD)
|
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT03935100 |
|
Recruitment Status :
Recruiting
First Posted : May 2, 2019
Last Update Posted : January 26, 2022
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Diverticular Disease | Procedure: Endoscopic clipping Other: Placebo - colonoscopy without clipping | Not Applicable |
Colonic diverticular disease (DD) is characterised by the presence of sac-like protrusions (diverticula), which form through defects in the muscle layer of the colon wall. It is prevalent in western countries, affecting approximately 70% of individuals by the age of 80. The risk of acquiring diverticular disease increases uniformly with age, with approximately 40% of people aged over 60 years affected in western countries. Diverticular complications may be severe and include pain, inflammation, infection and bleeding. Although the majority of people with diverticular disease are asymptomatic, approximately 25% will experience an episode of acute diverticulitis (the principal inflammatory complication of diverticulosis); of these, 15% will develop other significant and often serious complications such as abscess, fistula or perforation.
King's College Hospital operates a tertiary referral service for patients with diverticular disease that integrates a gastroenterological and colorectal surgical approach to treatment. The investigators increasingly find that many patients have characteristic DD pain and IBS like symptoms with or without a clearly defined episode of diverticulitis. The link between symptomatic diverticular disease and Irritable Bowel Symptoms is reflected to some extent in the literature, however, it remains a matter of significant controversy. Nevertheless, these symptoms are often difficult to control and can be debilitating. Current treatment options for the IBS like symptoms in symptomatic uncomplicated DD are limited. In this age group, a low FODMAP diet, the mainstay treatment for IBS, is impractical and there are few if any controlled studies that address these issues. There is hence a need for alternative therapeutic options. Secondly, complications related to DD are associated with significant morbidity and mortality and comes at significant cost to the health service. At present there is no proven prophylactic intervention to prevent the complications.
The investigators have recently published the results of a feasibility study carried out at King's College Hospital, which assessed the effectiveness of elective endoscopic clipping of diverticula in patients with a history of significant diverticular bleeding. Here, all visible diverticula were closed endoscopically using 'Instinct' endoclips. A diverticula closure rate of 87.2% (129/148) was demonstrated at follow up colonoscopy. In this group, there were no post-procedural complications and no diverticula-associated symptoms reported up to the follow-up colonoscopy. Notably, incidental complete resolution of chronic left sided abdominal pain was noted in one of our subjects.
The investigators now propose the use of elective diverticular clipping in patients with symptomatic diverticulosis with a view to alter the natural history of the disease i.e. to prevent complications of the disease. At the same time the investigators wish to assess their symptomatic response. Patients with symptomatic diverticular disease will be eligible. The trial will be carried out at King's College Hospital endoscopy suite, a tertiary referral centre for endoscopic procedures. The study will include 84 patients. Each patient will be in the study for a period of 12 months.
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 84 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Single (Participant) |
| Masking Description: | Blinded to clipping, undergo same procedure |
| Primary Purpose: | Treatment |
| Official Title: | A Prospective Randomised Placebo Controlled Trial on Prophylactic Endoscopic Clipping of Colonic Diverticula (PECoD) |
| Actual Study Start Date : | September 1, 2019 |
| Estimated Primary Completion Date : | January 17, 2022 |
| Estimated Study Completion Date : | April 1, 2023 |
| Arm | Intervention/treatment |
|---|---|
|
Experimental: Treatment Group
All visible diverticula clipped during index colonoscopy
|
Procedure: Endoscopic clipping
Endoscopic clips fired to close mucosa over diverticular defects. |
|
Placebo Comparator: Control Group
5 clips fired at random into colon lumen. No diverticula closed.
|
Other: Placebo - colonoscopy without clipping
Colonoscopy performed, no clipping of diverticula |
- Rate of diverticula closure [ Time Frame: 12 months ]Number of diverticula pre and post clipping
- Changes in abdominal symptoms [ Time Frame: 12 months ]Changes in abdominal symptoms as assessed by the Irritable Bowel Syndrome Symptom Severity Score before and at 3, 6 and 12 months
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years to 90 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Confirmed symptomatic diverticular disease (5 or more diverticula)
- Age range 18-90 years
- Retains capacity and medically fit for colonoscopy
Exclusion Criteria:
- Does not meet inclusion criteria
- Unable to give informed consent
- Patients with severe co-morbidities and substance misuse
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03935100
| United Kingdom | |
| King's College Hospital | Recruiting |
| London, United Kingdom, SE5 9RS | |
| Contact: Sophie Williams 02032998773 sophie.williams15@nhs.net | |
| Contact: Simbisai Ratcliff 02032998773 simbisai.ratcliff@nhs.net | |
| Responsible Party: | King's College Hospital NHS Trust |
| ClinicalTrials.gov Identifier: | NCT03935100 |
| Other Study ID Numbers: |
253898 |
| First Posted: | May 2, 2019 Key Record Dates |
| Last Update Posted: | January 26, 2022 |
| Last Verified: | January 2022 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
|
Diverticulum Diverticular Diseases Gastroenteritis |
Gastrointestinal Diseases Digestive System Diseases Pathological Conditions, Anatomical |

