Effect of Luteal Progesterone Support on Pregnancy Rates With Combined Clomid/ Gonadotropin & IUI

Stopped early · Phase 1

Conditions studied: Pregnancy

In brief

To determine the difference in clinical pregnancy rates with and without luteal progesterone support in a young reproductive aged population having undergone ovulation induction with combined clomiphene citrate and gonadotropin protocol with intrauterine insemination.

Key facts

Study ID

NCT02510534

Run by

Northwest Center for Infertility and Reproductive Endocrinology

People needed

520

Starts

2015-07-01

Expected to finish

2016-04-01

Last updated by the study team

2016-09-23

Who can join

Age: 18 and older, up to 37. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Age 18-37
• BMI 19-34 kg/m2
• Day 2-3 Follicle stimulating hormone (FSH) less than 10IU/mL
• Estradiol (E2) less than 80 pg/mL
• Anti-mullerian hormone (AMH) more than 1.5 ng/mL; or antral follicle count (AFC) up to 10
• Two patent fallopian tubes confirmed by hysterosalpingogram (HSG) or chromopertubation
• Normal uterine cavity confirmed by HSG, saline sonohysterogram (SIS) or hysteroscopy

You may not qualify if…

• Severe male factor (total count less than 10 million sperm)
• Systemic diseases not limited to diabetes
• Pregnancy within 3 months
• More than 1 prior cycle of gonadotropin treatment
• Any ovarian cyst >15mm that has persisted for > 1 month
• Endometrioma and/or Endometriosis-stage III or IV
• Submucosal uterine fibroids; untreated endometrial polyps >1 cm;abnormal reproductive tract bleeding
• Intolerance or allergy to study drug
• Substance abuse (including alcohol and tobacco)
• History of chemotherapy (except for gestational conditions) or radiotherapy
• Minors and those adults not capable of consenting on their own

Where it is running

• Ivf Florida — Margate, Florida, United States

Full record on ClinicalTrials.gov

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