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NCT03353012
Acceptability & Tolerance of Immediate Versus Delayed Postpartum Contraceptive Implant
Phase 4 trial testing Etonogestrel Drug Implant in Breastfeeding in 60 participants. Completed in 1 August 2018.
1 May 2018
Quick facts
| Lead sponsor | Chulalongkorn University |
|---|---|
| Phase | Phase 4 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 60 |
| Start date | 1 January 2018 |
| Primary completion | 1 May 2018 |
| Estimated completion | 1 August 2018 |
| Sites | 1 location across Thailand |
Drugs / interventions tested
- Etonogestrel Drug Implant — full drug profile →
- Levonorgestrel Drug Implant — full drug profile →
Conditions studied
- Breastfeeding — all drugs for Breastfeeding →
- Post Partum — all drugs for Post Partum →
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):
-
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:
- PubMed search for NCT03353012
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03353012 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Chulalongkorn University
- Last refreshed: 26 July 2019
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03353012.
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