Comparison between the synergistic use of oral contraceptives and fluoxetine vs fluoxetine alone in the management of premenstrual syndrome

Phase 3

Recruiting

• Conditions: Premenstrual syndrome; Reproductive Health and Childbirth - Menstruation and menopause

• Registration Number: ACTRN12614001243606
• Lead Sponsor: Cairo university

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2014-11-27
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 210

Inclusion Criteria

Age 20-40 years
Premenstrual syndrome
Nulligravida

Exclusion Criteria

Diabetes
Hypertension
Liver disease
History of DVT
Allergy to fluoxetine

Study & Design

• Study Type: Interventional
• Study Design: Not specified