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Acceptability & Tolerance of Immediate Versus Delayed Postpartum Contraceptive Implant

Breastfeeding Clinical Trial

Official title:
Acceptability & Tolerance of Immediate Versus Delayed Postpartum Contraceptive Implant

Clinical Trial Summary

To study and compare acceptability and tolerance between breast-feeding post-partum woman, who receive contraceptive implant 48-72 hours after giving birth or at 5-7 weeks after giving birth, using either Levonorgestrel or Etonogestrel contraceptive implant.

Clinical Trial Description

- To study and compare acceptability and tolerance between breast-feeding post-partum woman, who receive contraceptive implant 48-72 hours after giving birth or at 5-7 weeks after giving birth, using either Levonorgestrel or Etonogestrel contraceptive implant.

- Participants who wish to attend the study will be invited to choose between Levonorgestrel and Etonogestrel contraceptive implant, then they will be randomized into immediate postpartum or delay postpartum group. They will be follow-up at 6 and 12 weeks after receive contraceptive implant.

- Information about side effects, breastfeeding status, child growth, acceptability and tolerance will be noted using medical records and interviewing, gathering on paper case record forms.

- Sample size N = 60 (30 in each group (Immediate and delay postpartum group, 15 in each subgroup (Levonogestrel and Etonogestrel group)) This number of sample size is already counted with 10% data loss ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03353012
Study type Interventional
Source Chulalongkorn University
Contact
Status Completed
Phase Phase 4
Start date January 1, 2018
Completion date August 1, 2018
View Details
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