Drospirenone Only Pills and Cervical Mucus Changes: A Pre- and Post-Bariatric Surgery Study
Recruiting · NCT06345586 · Interventional (participants receive a specific treatment) · Lead sponsor: Chulalongkorn University
View the official record on ClinicalTrials.gov →Interventions studied
Drospirenone
What this trial is about
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
Who can take part
Age range
18 Years to 45 Years
Sex
Female
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Thai women aged 18-45 years who are obese and had an appointment for Bariatric surgery at Chulalongkorn Hospital
- Need contraception
- Able to use non-hormonal contraception during the study
- Giving consent
Exclusion criteria
- Pregnancy or history of giving birth within 3 months
- Breastfeeding within the 6 months
- History of using DMPA within 12 months
- History of using other types of hormonal birth control pills within 4 weeks
- History of bilateral oophorectomy or hysterectomy
- Suspected ovarian tumor or pathological ovarian cyst
- Regular cigarette smoking
- Contraindications to Drospirenone
Where it is running
1 location listed.
- Chulalongkorn University - Bangkok, Thailand