Completed
Effectiveness of Non-hormonal Treatment on Moderate to Severe Premenstrual Syndrome
- Status
- Completed
- Registry ID
- NCT07078708
- Type
- Interventional (tests a treatment)
- Phase
- NA
- Conditions
- Premenstrual Syndrome-PMS
- What is tested
- vitamin D (cholecalciferol) supplementation (dietary_supplement); Placebo (other)
- Sponsor
- Haleema Sadia
- Where
- Pakistan
- Participants
- 100
- Start
- 2024-06-01
- Completion
- 2024-11-30
- Last update
- 2025-07-22
About the study
A double-blind, randomised, placebo-controlled, parallel trial was conducted involving 100 females aged 18-40, all of whom presented with premenstrual syndrome at the Department of Gynecology and Obstetrics, Avicenna Medical College Hospital, Lahore, Pakistan. Participants were randomly assigned to two groups of equal size: One group received vitamin D supplementation at a dose of 50,000 IU every two weeks along with a daily intake of 1,000 mg of calcium, whereas the comparison group was administered a placebo under the same conditions for 12 weeks. All the participants were examined on premenstrual syndrome with the Premenstrual Symptoms Screening Tool-Adolescent (PSST-A) questionnaire
Summary from ClinicalTrials.gov.