Overview

Phytoestrogen, NO Donors, N-acetyl Cysteine Add Therapy to Clomiphene Citrate to Improve Pregnancy Rate in PCO Patients

Status:
Unknown status
Trial end date:
2015-12-01
Target enrollment:
0
Participant gender:
Female
Summary
To evaluate the effect of oral Phytoestrogen or Isosorbid mononitrate or N-acetyl cysteine as an adjuvant to clomiphene citrate on induction of ovulation and pregnancy outcomes in patients with PCOS. In this three-arm open RCT, 240 PCOS infertile women were randomly divided to 3 groups for induction of ovulation. Group A, [PE group, n= 80] patients received CC 100mg/d plus oral Phytoestrogen120 mg/ day and patients in Group B, [ISMN group, n=80] received CC 100 mg/d plus 20 mg Isosorbid mononitrate and Group C, [NAC group, n=80] patients received CC 100 mg/d plus NAC 1200 mg/day.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Kasr El Aini Hospital
Treatments:
Acetylcysteine
Clomiphene
N-monoacetylcystine
Phytoestrogens
Criteria
Inclusion Criteria:

1. All patients have PCOS.

2. All patients received CC 100 mg/day for 5 days starting from day 5 with successful
ovulation as documented by folliculometry and midluteal serum progesterone with no
pregnancy achieved.

3. All patients have patent fallopian tubes by Hysterosalpingography.

4. Their husbands have normal semen analysis according to the modified criteria of WHO.

5. All patients have normal serum prolactin and thyroid profile.

6. Any patient having vaginitis was treated before starting induction.

Exclusion Criteria:

1. Other causes of infertility than anovulation.

2. Diabetes or other endocrinological disorders.

3. Age > 40 years.

4. Smoking.

5. Alcohol use.

6. Presence of ovarian cyst >2cm on the second day of the cycle.

7. Patients who have received gonadotrophins in the preceeding 6 months.

8. Patients who have done unilateral or bilateral ovarian drilling.

9. Allergy to PE, NO donors or NAC