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NCT03353012

Acceptability & Tolerance of Immediate Versus Delayed Postpartum Contraceptive Implant

Completed Phase 4 Last updated 26 July 2019
What this trial tests

Phase 4 trial testing Etonogestrel Drug Implant in Breastfeeding in 60 participants. Completed in 1 August 2018.

Timeline
1 January 2018
Primary endpoint
1 May 2018
1 August 2018

Quick facts

Lead sponsorChulalongkorn University
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment60
Start date1 January 2018
Primary completion1 May 2018
Estimated completion1 August 2018
Sites1 location across Thailand

Drugs / interventions tested

Conditions studied

Sponsor

Chulalongkorn University

Who can join

Adults 18 to 45, female only, with Breastfeeding or Post Partum. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own 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.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Immediate versus delayed postpartum insertion of contraceptive implant and IUD for contraception.
    Sothornwit J, Kaewrudee S, Lumbiganon P, Pattanittum P, et al · · 2022 · cited 12× · PMID 36302159 · DOI 10.1002/14651858.cd011913.pub3

Verify or expand the search:

Other recruiting trials for Breastfeeding

Currently open trials in the same condition.

Other Chulalongkorn University trials

Trials by the same sponsor.

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