MedPath

The effect of supplementation on the combined pill continuation rate and Harassment rate of its side effects

Not Applicable
Conditions
continuation rate of oral contraceptives.
oral contraceptives
Registration Number
IRCT201210093706N15
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
330
Inclusion Criteria

married no pregnant women aged 18-40 years; intention to start using Low dose (LD) combined pills as a contraceptive method; being literate; not taking combined hormonal methods at least in the past three months.
Exclusion criteria: plan to get pregnant in 6 months; not having medical eligibility criteria for contraceptive use.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Continuation rate. Timepoint: monthly. Method of measurement: interview.;Harrasement rate of side effects of the pills. Timepoint: daily. Method of measurement: interview.
Secondary Outcome Measures
NameTimeMethod
Correct use of the pills. Timepoint: monthly. Method of measurement: interview.
© Copyright 2025. All Rights Reserved by MedPath