Serum Anti-mullerian Hormone and Polycystic Ovarian Syndrome
The Impact of Serum Antimullerian Hormone Level on Adjusting the Number of Ovarian Drills in Polycystic Ovarian Syndrome
1 other identifier
interventional
50
1 country
1
Brief Summary
In 1935 the polycystic ovary syndrome was a clinical diagnosis made on the morphological appearance of the ovaries in association with amenorrhoea, hirsutism and frequently obesity. At that time wedge resection of the ovaries was introduced on an empirical basis and proved a successful treatment for the associated anovulation and infertility. In the ensuing fifty years the limitations of a purely surgical approach to therapy have become recognized and the importance of the biochemical abnormalities appreciated. Prevalence of polycystic Ovary Syndrome: The prevalence of polycystic ovary syndrome in any specified population is dependent upon the diagnostic criteria used, but does have some regional and ethnic variation. While most reports on the prevalence of polycystic ovary syndrome range between 2 and 20%, the chosen diagnostic criteria are recognized to influence the determined prevalence. Anti-mullerian hormone which is a predictor of ovarian reserve is known to decrease after laparoscopic ovarian drilling. On the best of our knowledge no study had been done to use the level of anti-mullerian hormone as a factor for planning the number of ovarian drills in each ovary.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_2
Started Jan 2015
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
November 30, 2016
CompletedFirst Submitted
Initial submission to the registry
July 30, 2017
CompletedFirst Posted
Study publicly available on registry
August 2, 2017
CompletedAugust 2, 2017
July 1, 2017
1.7 years
July 30, 2017
July 30, 2017
Conditions
Outcome Measures
Primary Outcomes (1)
Size of ovarian follicle (mm)
14 days
Secondary Outcomes (2)
Antimullerian hormone level (ng/dl)
3 months
Ovarian volume (ml)
3 months
Study Arms (2)
The control group
OTHERFour punctures in each ovary were done regardless of the level of antimullerian hormone
The study group
OTHERThe number of ovarian drills was adjusted according to antimullerian hormone level
Interventions
The electric current used was set at 40 Watts. The power was activated just before touching the ovary, and then the needle electrode was held against the antimesenteric surface of the ovary for 4 seconds until penetration of the ovarian capsule. Four or eight puncture points were made through the ovarian capsule of each ovary according to the study protocol. The ovaries were cooled in the pool of the Ringer's lactate after each cauterization both to minimize adhesion formation and to prevent heat trauma to the adjacent viscera. Complete hemostasis was ensured. At the end of the procedure, the ovaries were copiously rinsed with Ringer's lactate (Aqua-purator, Storz, Germany). An amount about 200 ml of heparinized Ringers lactate (5000 IU/1000 ml) was left in the pelvis to avoid postoperative adhesions.
1. In patients with Antimullerian hormone between 4-8 ng/ml 4 punctures in each ovary were performed. 2. In patients with Antimullerian hormone above 8 ng/ml 8 punctures in each ovary were performed.
Eligibility Criteria
You may qualify if:
- Infertility more than 2 years.
- Age between 20-35 years.
- clomiphene resistant patients: Patients received clomiphene 150 mg from day 3 to 7 of the menstrual cycle for 6 months and non-ovulatory (with failure of conception). They were followed up in the outpatient clinic.
- No contraindications for laparoscopy.
- Normal Hysterosalpingography
You may not qualify if:
- Contraindications for laparoscopy e.g cardiac diseases, bad scared abdomen ect….
- Women's age less than 20 years or more than 35 years.
- Previous Laparoscopic surgery.
- Previous ovarian surgery.
- Women with Antimullerian hormone level less than 4 ng/ml.
- Tubal factor infertility as diagnosed by Hysterosalpingography .
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Women Health Hospital - Assiut university
Asyut, 71111, Egypt
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr
Study Record Dates
First Submitted
July 30, 2017
First Posted
August 2, 2017
Study Start
January 1, 2015
Primary Completion
September 30, 2016
Study Completion
November 30, 2016
Last Updated
August 2, 2017
Record last verified: 2017-07