Gonadotropin-releasing Hormone (GnRH) Downregulation Versus Oral Anticonception Prior to ART in Postoperative Endometriosis Patients
Primary Purpose
Endometriosis, Infertility
Status
Unknown status
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
triptorelin
ethinylestradiol + dienogest
Sponsored by
About this trial
This is an interventional treatment trial for Endometriosis focused on measuring endometriosis, infertility, assisted reproductive technology
Eligibility Criteria
Inclusion Criteria:
- histologically proven endometriosis with complete treatment of all endometriosis lesions during laparoscopy
- only first three ART cycles
- normal uterine cavity
- Eligible for ovarian stimulation with long agonist protocol
Exclusion Criteria:
- FSH>20 IU/L
- presence of large intramural fibroids (> 3 cm)
- <4 oocytes obtained in any previous fresh ART cycle
- ART with sperm derived from testicular biopsy
- ART with Preimplantation Genetic Diagnosis/Screening
Sites / Locations
- UZ Leuven
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
oral oestroprogestogen pre-treatment
gonadotropin-releasing hormone (GnRH) pre-treatment
Arm Description
preparation with oral oestroprogestogens prior to downregulation in an assisted reproductive technology treatment (ART) cycle
preparation with gonadotropin-releasing hormone (GnRH) analogues prior to downregulation in an assisted reproductive technology treatment (ART) cycle
Outcomes
Primary Outcome Measures
clinical pregnancy rate per initiated ART cycle
Secondary Outcome Measures
Full Information
NCT ID
NCT02400801
First Posted
March 11, 2015
Last Updated
June 8, 2017
Sponsor
Universitaire Ziekenhuizen KU Leuven
1. Study Identification
Unique Protocol Identification Number
NCT02400801
Brief Title
Gonadotropin-releasing Hormone (GnRH) Downregulation Versus Oral Anticonception Prior to ART in Postoperative Endometriosis Patients
Study Type
Interventional
2. Study Status
Record Verification Date
June 2017
Overall Recruitment Status
Unknown status
Study Start Date
June 2013 (undefined)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
December 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universitaire Ziekenhuizen KU Leuven
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Does prolonged GnRH downregulation prior to ART improve the clinical pregnancy rate in postoperative endometriosis patients? (A single centre randomised controlled trial)
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endometriosis, Infertility
Keywords
endometriosis, infertility, assisted reproductive technology
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
166 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
oral oestroprogestogen pre-treatment
Arm Type
Active Comparator
Arm Description
preparation with oral oestroprogestogens prior to downregulation in an assisted reproductive technology treatment (ART) cycle
Arm Title
gonadotropin-releasing hormone (GnRH) pre-treatment
Arm Type
Experimental
Arm Description
preparation with gonadotropin-releasing hormone (GnRH) analogues prior to downregulation in an assisted reproductive technology treatment (ART) cycle
Intervention Type
Drug
Intervention Name(s)
triptorelin
Other Intervention Name(s)
decapeptyl
Intervention Description
gonadotropin-releasing hormone (GnRH) agonist
Intervention Type
Drug
Intervention Name(s)
ethinylestradiol + dienogest
Other Intervention Name(s)
Louise
Intervention Description
oral oestroprogestogen
Primary Outcome Measure Information:
Title
clinical pregnancy rate per initiated ART cycle
Time Frame
participants will be followed for the duration of the ART cycle including the pregnancy test, an expected average of 10 weeks in the active comparator group and an expected average of 18 weeks in the experimental group
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
39 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
histologically proven endometriosis with complete treatment of all endometriosis lesions during laparoscopy
only first three ART cycles
normal uterine cavity
Eligible for ovarian stimulation with long agonist protocol
Exclusion Criteria:
FSH>20 IU/L
presence of large intramural fibroids (> 3 cm)
<4 oocytes obtained in any previous fresh ART cycle
ART with sperm derived from testicular biopsy
ART with Preimplantation Genetic Diagnosis/Screening
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thomas M D'Hooghe, MD, PhD
Organizational Affiliation
UZ Leuven
Official's Role
Principal Investigator
Facility Information:
Facility Name
UZ Leuven
City
Leuven
ZIP/Postal Code
3000
Country
Belgium
12. IPD Sharing Statement
Citations:
PubMed Identifier
34370858
Citation
Tomassetti C, Beukeleirs T, Conforti A, Debrock S, Peeraer K, Meuleman C, D'Hooghe T. The ultra-long study: a randomized controlled trial evaluating long-term GnRH downregulation prior to ART in women with endometriosis. Hum Reprod. 2021 Sep 18;36(10):2676-2686. doi: 10.1093/humrep/deab163.
Results Reference
derived
Learn more about this trial
Gonadotropin-releasing Hormone (GnRH) Downregulation Versus Oral Anticonception Prior to ART in Postoperative Endometriosis Patients
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