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The effect of an educational video on immediate postpartum insertion of contraceptive implants : a randomized controlled trial

Phase 1
Completed
Conditions
Postpartum contraception
Postpartum
Contraceptive implant
Registration Number
TCTR20220720003
Lead Sponsor
Faculty of Medicine, Khon Kaen University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Female
Target Recruitment
202
Inclusion Criteria

Postpartum women who gave birth in Srinagarind Hospital who need irreversible contraception for at least 18 months.

Exclusion Criteria

1.Postpartum women who chose permanent contraception, including female sterilization or male sterilization.
2.Postpartum women who are contraindicated to the use of the contraceptive implant, including Deep vein thrombosis or pulmonary thromboembolism, unexplained vaginal bleeding, breast cancer, cirrhosis or liver tumors and SLE
3.Postpartum women who cannot communicate in Thai

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Contraceptive implant utilization at immediate postpartum at 24 hours after end of the intervention N/V
Secondary Outcome Measures
NameTimeMethod
Contraceptive implant utilization at 12 weeks postpartum at 12 weeks after end of the intervention N/V
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