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Randomized Clinical Trial on Follicular Flushing in IVF

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ClinicalTrials.gov Identifier: NCT02365350
Recruitment Status : Completed
First Posted : February 18, 2015
Last Update Posted : November 18, 2016
Sponsor:
Information provided by (Responsible Party):
Prof. Dr. med. M.Sc. Georg Griesinger, University of Luebeck

Brief Summary:
The primary objective is to demonstrate superiority of follicle flushing with the STEINER-TAN Needle® as compared to single lumen aspiration in terms of numbers of COCs retrieved.

Condition or disease Intervention/treatment Phase
Infertility Procedure: STEINER-TAN Needle® Procedure: 17 G single lumen needle Not Applicable

Detailed Description:

Rationale:

Since the number of oocytes available for IVF is a determinant of the cumulative chance of a patient to achieve pregnancy, it is of paramount importance to optimize the number of oocytes at oocyte pick-up. This especially for a fraction of patients, who despite high-dosed FSH stimulation, produce only a small number of growing follicles (poor response).

Objective:

The primary objective is to demonstrate superiority of follicle flushing with the STEINER-TAN Needle® as compared to single lumen aspiration in terms of numbers of COCs retrieved.

The secondary objective is to study differences in numbers of mature oocytes, proportion of patients undergoing embryo transfer, pregnancy rate, duration of the procedure, impact on patient burden (as assessed by the DASS 21, the German pain questionnaire [www.dgss.org]) and subjective patient experience.

Study design:

Prospective, single-center, randomized controlled, open trial comparing a 17G single lumen aspiration needle with a modified double lumen needle system (STEINER-TAN Needle®) for follicular flushing during oocyte pick-up in IVF patients with poor ovarian response.

Study population:

Patients with a BMI < 35 kg/m2 and an indication for IVF or ICSI with or without ovarian stimulation presenting with ≤ 5 follicles >10mm in the ovaries at the end of the follicular phase of the treatment cycle will be eligible for inclusion. Final oocyte maturation is to be induced by hCG administration as soon as the leading follicle reaches a mean diameter of 18mm or the day thereafter.

Intervention:

Eighty (n=80) patients will be randomly allocated on the day when the decision is taken to administer hCG to one of the following two procedures. In the study group all visible follicles regardless of size in both ovaries will be first aspirated and then flushed at least three times by the STEINER-TAN Needle® system. In the control group all visible follicles regardless of size in both ovaries will be aspirated by the 17G single lumen needle.

Main study parameters/endpoints:

The main study parameter/endpoint is the mean number of COSs per patient randomized.

Secondary endpoints are the mean number of mature metaphase II oocytes per patient and per COC retrieved per patient, the number of fertilized (2PN) oocytes, the fertilization rate (number of 2PN oocytes/number of injected or inseminates oocytes), the pregnancy rate (viable pregnancy at 6-7 gestational weeks/randomized patient), the mean DASS 21 score after the procedure, the mean duration of the procedure (min, sec), the COC retrieval rate per puncture follicle and the proportion of randomized patients not reaching embryo transfer. Furthermore, the patients will be interviewed about their overall experience of the procedure.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 80 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Randomized, Controlled, Open Trial Comparing a 17 G Single Lumen Aspiration Needle With a Modified Double Lumen Needle System (STEINER-TAN Needle®) for Follicular Flushing During Oocyte Pick-up in IVF Patients With Poor Ovarian Response
Study Start Date : January 2015
Actual Primary Completion Date : August 2016
Actual Study Completion Date : August 2016

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Tanning

Arm Intervention/treatment
Experimental: STEINER-TAN Needle®
All visible follicles regardless of size in both ovaries will be aspirated and flushed three times by the STEINER-TAN Needle.
Procedure: STEINER-TAN Needle®
A purpose built new double lumen needle with little dead space.

Active Comparator: 17G single lumen needle
In the control group all visible follicles regardless of size in both ovaries will be aspirated by the 17G single lumen needle.
Procedure: 17 G single lumen needle
A conventional single lumen IVF aspiration needle.




Primary Outcome Measures :
  1. Mean number of COSs per patient randomized. [ Time Frame: 1 day ]

Secondary Outcome Measures :
  1. Mean number of mature metaphase II oocytes [ Time Frame: 1 day ]
  2. Pregnancy rate [ Time Frame: 7 weeks ]
  3. Mean number of fertilized (2PN) oocytes [ Time Frame: 2 days ]
  4. Mean DASS 21 score after the procedure [ Time Frame: 1 day ]
  5. Mean duration of the procedure. [ Time Frame: 1 day ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 45 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Female subjects undergoing IVF or ICSI treatment with or without ovarian stimulation
  • ≤ 5 follicles >10 mm at the end of the follicular phase as assessed by transvaginal ultrasound
  • Presence of two ovaries
  • Willingness to participate
  • Informed consent

Exclusion Criteria:

  • BMI <18 or >35 kg/m2
  • Ovaries cannot be reached (e.g. heterotopic ovaries)
  • Age <18 or >45

Information from the National Library of Medicine

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): NCT02365350


Locations
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Germany
Universitäres Kinderwunschzentrum Lübeck
Lübeck, Schleswig Holstein, Germany, 23562
Sponsors and Collaborators
University of Luebeck
Investigators
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Principal Investigator: Georg Griesinger, MD MSc PhD University of Luebeck
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Responsible Party: Prof. Dr. med. M.Sc. Georg Griesinger, University of Luebeck
ClinicalTrials.gov Identifier: NCT02365350    
Other Study ID Numbers: 14-244
First Posted: February 18, 2015    Key Record Dates
Last Update Posted: November 18, 2016
Last Verified: November 2016
Additional relevant MeSH terms:
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Infertility
Flushing
Skin Manifestations