Comparison of the Effect of Subcutaneous Progesterone and Vaginal Progesterone for Luteal Phase Support

• Status: Not yet recruiting
• Trial end date: 2022-11-01
• Target enrollment: 0
• Participant gender: Female

Summary

The invesigators aimed to seperate the patients,which is going to be applied IUI, to two different groups as prospective randomized controlled ;assess the efficacy of the two different way pressurised progesterone by appling intravaginal progesterone to the first group; subcutaneous to the second group.

• Phase: N/A
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Bezmialem Vakif University
• Treatments: Progesterone

Criteria

Inclusion Criteria:

• Absence of follicles larger than 10 mm on basal ultrasound

• Endometrial thickness less than 5 mm

• Patients with FSH<10 IU/ml, E2<60-80 pg/ml in the blood hormone test performed on the third day of the cycle and patients with antral follicle count above 7 on ultrasound

• Total motile sperm count greater than 10 million/ml

• 18-40 years old female, 18-50 years old male

• Anovulation, patients diagnosed with unexplained mild male factor infertility

• Female partners, who's BMI<25 kg/m²

• Being voluntarily

Exclusion Criteria:

• Other infertility reasons

• The patients who doesn't meet the criterias

• Refusing to attend to the research