LOD vs Gn in Anovulatory PCOs Resistant to First Line Agents
Primary Purpose
Polycystic Ovary Syndrome, Anovulation
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Laparoscopic ovarian drilling
Recombinant FSH (rFSH)
Sponsored by
About this trial
This is an interventional treatment trial for Polycystic Ovary Syndrome focused on measuring Laparoscopic ovarian drilling, Gonadotrophins, Polycystic ovary syndrome, Anovulation, PCOs, Clomiphene resistant, Letrozole resistant
Eligibility Criteria
Inclusion Criteria:
anovulatory polycystic ovary syndrome resistant to first line ovulation induction.
- Polycystic ovary Syndrome defined by Rotterdam's criteria 2003
- Clomiphene resistance defined as failure to ovulate with a dose of 150mg per day for 5 days for 3 cycles
- Letrozole resistance defined as failure to ovulate with a dose of 7.5 mg per day for 5 days for 3 cycles
Exclusion Criteria:
- women's age < 18 years or ≥ 40 years.
- BMI > 40 kg/m2
- Patient with hyperprolactinaemia (serum prolactin above normal limits)
- Patients with hypogonadotropic hypogonadism (low serum FSH and LH)
- Patients with anovulation due to ovarian failure (serum FSH higher than normal limits)
- Male infertility
- Tubal abnormality, Known endometriosis, adenomyosis, uterine myomas or any other detected cause of female infertility
- History of ovarian surgery as laparoscopic ovarian drilling, ovarian cystectomy or oophorectomy
- History of pelvic radiation
- Patient recently treated with any type of induction of ovulation in the last three months.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Surgical treatment strategy:
Gonadotrophins treatment strategy
Arm Description
Outcomes
Primary Outcome Measures
Live Birth
defined as the number of births resulted in live babies after the age of viability (24th week of pregnancy)
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04325295
Brief Title
LOD vs Gn in Anovulatory PCOs Resistant to First Line Agents
Official Title
Laparoscopic Ovarian Drilling Versus Gonadotrophins for Anovulatory Polycystic Ovary Syndrome Resistant to First Line Ovulation Induction: a Randomized Controlled Trial.
Study Type
Interventional
2. Study Status
Record Verification Date
October 2020
Overall Recruitment Status
Unknown status
Study Start Date
December 2020 (Anticipated)
Primary Completion Date
June 2022 (Anticipated)
Study Completion Date
August 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Assiut University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
PCOS is a complex disease that is diagnosed by the presence of two of the following three: oligo/anovulation, clinical and/or biochemical hyperandrogenism, or polycystic ovaries by ultrasound . PCOS affects 4% to 21% of females in reproductive age . Although subfertility is abundant in women with PCOS, a majority of these women will achieve pregnancy naturally or by treatment.
Different treatment modalities are present for ovulation induction. Life style modifications including weight loss are encouraged for those who are overweight or obese. Pharmacological induction of ovulation represent the first line therapy for induction of ovulation. Options include aromatase inhibitors (Letrozole), Clomiphene Citrate (CC) or Metformin, alone or in combinations.
For second line treatment either Gonadotropins (Gn) or laparoscopic ovarian surgery (LOS) are the recommended options .
the objective of the trial is to study the effectiveness and safetey of surgical induction of ovulation strategy and compare it to medical induction strategy with Gonadotropins
Detailed Description
PCOS is a complex disease that is diagnosed by the presence of two of the following three: oligo/anovulation, clinical and/or biochemical hyperandrogenism, or polycystic ovaries by ultrasound . PCOS affects 4% to 21% of females in reproductive age . Although subfertility is abundant in women with PCOS, a majority of these women will achieve pregnancy naturally or by treatment.
Different treatment modalities are present for ovulation induction. Life style modifications including weight loss are encouraged for those who are overweight or obese. Pharmacological induction of ovulation represent the first line therapy for induction of ovulation. Options include aromatase inhibitors (Letrozole), Clomiphene Citrate (CC) or Metformin, alone or in combinations.
For second line treatment either Gonadotropins (Gn) or laparoscopic ovarian surgery (LOS) are the recommended options .
Systematic reviews done comparing LOD to Gn found no differences in live birth, clinical pregnancy or miscarriage rates. However, there was significant decrease in OHSS and multiple pregnancies with LOD . Giving these advantages together with being cheap, the surgical strategy may be a more favorable choice as second line treatment of anovulation . Also several randomised controlled trial (RCTs) reported normalization of ovarian reserve parameters after LOD, making it a long-lasting option compared to the one-cycle effect of medical treatment the objective of the trial is to study the effectiveness and safetey of surgical induction of ovulation strategy and compare it to medical induction strategy with Gonadotropins
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polycystic Ovary Syndrome, Anovulation
Keywords
Laparoscopic ovarian drilling, Gonadotrophins, Polycystic ovary syndrome, Anovulation, PCOs, Clomiphene resistant, Letrozole resistant
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Surgical treatment strategy:
Arm Type
Active Comparator
Arm Title
Gonadotrophins treatment strategy
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
Laparoscopic ovarian drilling
Intervention Description
LOD will be done in the follicular phase.Follow up will be done on the next cycle by performing a TVUS examination at CD 13 and measuring the dominant follicles. Ovulation is considered if a follicle reached > 17 mm and is confirmed by measuring serum progesterone at CD 21.If ovulation is not achieved in the cycle following LOD, women will be prescribed Letrozole by the dose of 2.5 mg daily for 5 days starting from CD 3, and ovulation monitoring will be done similarly. If ovulation is not achieved, the dose is increased by 2.5 mg daily in the subsequent cycle until reaching the maximum dose of 7.5 mg daily for a total of 3 cycles.With persistent resistance to Letrozole in inducing ovulation, Gn will be prescribed for 3 cycles as in Gonadotrophin strategy
Intervention Type
Drug
Intervention Name(s)
Recombinant FSH (rFSH)
Intervention Description
A low-dose step-up protocol will be implemented. This starts on CD 3,The rFSH will be given through (IM) or(SC) injections with 75 IU and will be given once daily.Monitoring of the treatment will be done on CD 7 by TVUS and serum E2. Monitoring is individualized according to the response. Depending on the response and follicular growth, the dose may be adjusted by increasing 37.5 IU. If follicular growth failed, the dose is furtherly increased by the same amount until at least one follicle reaches 10 mm. The dose is maintained until at least one follicle reaches a diameter of 18 mm and no more than 2 follicles are bigger than 15 mm. Once reaching the desired diameter, the rFSH will be stopped and a trigger of ovulation by an IM injection of 5000 IU of hCG and sexual intercourse is encouraged on the day of trigger and the next day. Then serum P will be done 7 days after hCG injection to detect the occurrence of ovulation.
Primary Outcome Measure Information:
Title
Live Birth
Description
defined as the number of births resulted in live babies after the age of viability (24th week of pregnancy)
Time Frame
within 12 months after of end treatment strategy
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
anovulatory polycystic ovary syndrome resistant to first line ovulation induction.
Polycystic ovary Syndrome defined by Rotterdam's criteria 2003
Clomiphene resistance defined as failure to ovulate with a dose of 150mg per day for 5 days for 3 cycles
Letrozole resistance defined as failure to ovulate with a dose of 7.5 mg per day for 5 days for 3 cycles
Exclusion Criteria:
women's age < 18 years or ≥ 40 years.
BMI > 40 kg/m2
Patient with hyperprolactinaemia (serum prolactin above normal limits)
Patients with hypogonadotropic hypogonadism (low serum FSH and LH)
Patients with anovulation due to ovarian failure (serum FSH higher than normal limits)
Male infertility
Tubal abnormality, Known endometriosis, adenomyosis, uterine myomas or any other detected cause of female infertility
History of ovarian surgery as laparoscopic ovarian drilling, ovarian cystectomy or oophorectomy
History of pelvic radiation
Patient recently treated with any type of induction of ovulation in the last three months.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Khaled M Attyia
Phone
+201005503250
Email
khaled.hussien@med.aun.edu.eg
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sayed A Abdallah
Organizational Affiliation
Professor of obstetric and Gynecology,Faculty of Medicine,Assuit University O
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Essam R Othman
Organizational Affiliation
Assistant Professor of Obstetrics and Gynecology,Faculty of Medicine, Assuit University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Mustafa B Mohammed
Organizational Affiliation
Assistant professor of Obstetrics and Gynecology, Faculty of Medicine,Assuit University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Ahmed M Alaa Eldin
Organizational Affiliation
Lecturer of Obstetrics and Gynecology,Faculty of Medicine,Assuit University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Karim S Abdallah
Organizational Affiliation
Assistant lecturer of Obstetrics and Gynecology,Faculty of Medicine,Assuit University
Official's Role
Study Director
12. IPD Sharing Statement
Citations:
PubMed Identifier
30679436
Citation
Farquhar CM, Bhattacharya S, Repping S, Mastenbroek S, Kamath MS, Marjoribanks J, Boivin J. Female subfertility. Nat Rev Dis Primers. 2019 Jan 24;5(1):7. doi: 10.1038/s41572-018-0058-8.
Results Reference
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PubMed Identifier
30648738
Citation
Weiss NS, Kostova E, Nahuis M, Mol BWJ, van der Veen F, van Wely M. Gonadotrophins for ovulation induction in women with polycystic ovary syndrome. Cochrane Database Syst Rev. 2019 Jan 16;1(1):CD010290. doi: 10.1002/14651858.CD010290.pub3.
Results Reference
background
PubMed Identifier
27233760
Citation
Lizneva D, Suturina L, Walker W, Brakta S, Gavrilova-Jordan L, Azziz R. Criteria, prevalence, and phenotypes of polycystic ovary syndrome. Fertil Steril. 2016 Jul;106(1):6-15. doi: 10.1016/j.fertnstert.2016.05.003. Epub 2016 May 24.
Results Reference
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PubMed Identifier
15242999
Citation
van Wely M, Bayram N, Bossuyt PM, van der Veen F. Laparoscopic electrocautery of the ovaries versus recombinant FSH in clomiphene citrate-resistant polycystic ovary syndrome. Impact on women's health-related quality of life. Hum Reprod. 2004 Oct;19(10):2244-50. doi: 10.1093/humrep/deh406. Epub 2004 Jul 8.
Results Reference
background
PubMed Identifier
19347705
Citation
Api M. Is ovarian reserve diminished after laparoscopic ovarian drilling? Gynecol Endocrinol. 2009 Mar;25(3):159-65. doi: 10.1080/09513590802585605.
Results Reference
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PubMed Identifier
31497757
Citation
Debras E, Fernandez H, Neveu ME, Deffieux X, Capmas P. Ovarian drilling in polycystic ovary syndrome: Long term pregnancy rate. Eur J Obstet Gynecol Reprod Biol X. 2019 Aug 13;4:100093. doi: 10.1016/j.eurox.2019.100093. eCollection 2019 Oct.
Results Reference
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PubMed Identifier
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Citation
Amer SA, Banu Z, Li TC, Cooke ID. Long-term follow-up of patients with polycystic ovary syndrome after laparoscopic ovarian drilling: endocrine and ultrasonographic outcomes. Hum Reprod. 2002 Nov;17(11):2851-7. doi: 10.1093/humrep/17.11.2851.
Results Reference
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PubMed Identifier
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Citation
Farquhar C, Brown J, Marjoribanks J. Laparoscopic drilling by diathermy or laser for ovulation induction in anovulatory polycystic ovary syndrome. Cochrane Database Syst Rev. 2012 Jun 13;(6):CD001122. doi: 10.1002/14651858.CD001122.pub4.
Results Reference
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PubMed Identifier
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Citation
Nahuis MJ, Oude Lohuis E, Kose N, Bayram N, Hompes P, Oosterhuis GJ, Kaaijk EM, Cohlen BJ, Bossuyt PP, van der Veen F, Mol BW, van Wely M. Long-term follow-up of laparoscopic electrocautery of the ovaries versus ovulation induction with recombinant FSH in clomiphene citrate-resistant women with polycystic ovary syndrome: an economic evaluation. Hum Reprod. 2012 Dec;27(12):3577-82. doi: 10.1093/humrep/des336. Epub 2012 Sep 20.
Results Reference
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LOD vs Gn in Anovulatory PCOs Resistant to First Line Agents
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