Drospirenone Only Pills and Cervical Mucus Changes: A Pre- and Post-Bariatric Surgery Study

ConditionContraception
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-45
SponsorChulalongkorn University

About this trial

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

Eligibility criteria

Qualifiers

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

Disqualifiers

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

Trial design

Treatments tested in this trial

  • Drospirenone

Treatment groups

16 Participants
are divided into 1 treatment group

Sponsors and collaborators