Trials / Recruiting
RecruitingNCT06345586
Drospirenone Only Pills and Cervical Mucus Changes: A Pre- and Post-Bariatric Surgery Study
Drospirenone Only Pills and Cervical Mucus Changes in Obese Thai Women: A Pre- and Post-Bariatric Surgery Study
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 16 (estimated)
- Sponsor
- Chulalongkorn University · Academic / Other
- Sex
- Female
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to study the effect of Drospirenone on cervical mucus change by modified Insler score, pre-bariatric surgery and post-bariatric surgery
Detailed description
After being informed about the study and potential risks, all participants giving written informed consent who meet the eligibility requirements will take Drospirenone-only pills (4 mg, once daily). Cervical mucus by modified Insler score will be evaluated on Day 4-7 of Drospirenone taking. Pre-bariatric surgery results will be compared with post-bariatric surgery results.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Drospirenone | 4 mg tablet once daily |
Timeline
- Start date
- 2024-04-18
- Primary completion
- 2026-07-01
- Completion
- 2026-07-01
- First posted
- 2024-04-03
- Last updated
- 2026-03-18
Locations
1 site across 1 country: Thailand
Source: ClinicalTrials.gov record NCT06345586. Inclusion in this directory is not an endorsement.