Unexplained Infertility Clinical Trial
Official title:
The Effect of Endometrial Scratching by Pipelle on Pregnancy Rate in Couples With Unexplained Infertility
Research question:
Population: women with unexplained infertility. Intervention: endometrial scratching by
pipelle for women with unexplained infertility.
Comparison: to compare with non endometrial scratching for women with unexplained
infertility.
Outcome: the biochemical pregnancy rate.
Research hypothesis:
Null hypothesis: there is no difference in the rate of pregnancy between scratching and non
endometrial scratching in women with unexplained infertility.
Alternative hypothesis: there is difference in the rate of pregnancy between scratching and
non endometrial scratching in women with unexplained infertility.
Status | Recruiting |
Enrollment | 158 |
Est. completion date | June 2014 |
Est. primary completion date | June 2014 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 20 Years to 35 Years |
Eligibility |
Inclusion Criteria 1. Women diagnosed to have unexplained infertility aged between 20-35y. 2. Regular menstruation with the length of the cycle between 21-35 days. 3. Ovulation confirmed by appropriately timed mid-luteal progesterone. 4. Fertile semen variables (according to world health organization criteria 2010). 5. Bilateral tubal patency (demonstrated by laparoscopy or hystrosalpingography). Exclusion Criteria: 1- Patients aged less than 20 y. or more than 35y 2- Infertile semen analysis. 3- Abnormal hormonal profile (FSH level more than 10). 4- Patient diagnosed as polycystic ovary (PCO). 5- Medical disorders as hypertention,liver and renal diseases. 6- Endocrinal disorders as hyperthyroidism,hypothyroidism and diabetes mellitus. 7- Pelvic pathology as PID or uterine fibroids. 8- No previous history or planning for IVF. 9- Unwilling to comply with the protocol. 10- Participation in another clinical trial in the last 3 months prior to the start of this study. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Egypt | Ain Shams Maternity Hospital | Cairo |
Lead Sponsor | Collaborator |
---|---|
Ain Shams University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Biochemical Pregnancy Rate in Scratching and Non Endometrial Scratching Group. | six months | No |
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