Last reviewed · How we verify

NCT03404622

Immediate Post-placental Insertion of IUCD During Cesarean Delivery Versus 6 Week Post-Cesarean Insertion

Completed Phase 1 Last updated 29 January 2018
What this trial tests

Phase 1 trial testing IUCD in Mechanical Complication of Intrauterine Device in 200 participants. Completed in 20 December 2017.

Timeline
20 September 2016
Primary endpoint
20 December 2016
20 December 2017

Quick facts

Lead sponsorALshaimaa Aboalhassan Ali
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposehealth services research
Enrollment200
Start date20 September 2016
Primary completion20 December 2016
Estimated completion20 December 2017
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

ALshaimaa Aboalhassan Ali — full company profile →

Who can join

Adults 18 to 45, female only, with Mechanical Complication of Intrauterine Device. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of current study is to compare the rates of IUCD expulsion and complications in immediate post-placental insertion versus delayed IUCD insertion (6-weeks after cesarean delivery)

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:

Verify against primary sources

Data sources for this page

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/NCT03404622.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing