NCT02957292View on ClinicalTrials.gov

A Study to Compare the Menstrual Bleeding Profile Among Jaydess® and Copper Intrauterine Device (IUD) Users. COLIBRI STUDY (Copper and Levonorgestrel IUD Barcelona Research Initiative).

PHASE4CompletedINTERVENTIONAL
Enrollment

108

Participants

Timeline

Start Date

June 1, 2016

Primary Completion Date

September 15, 2020

Study Completion Date

September 15, 2020

Conditions
Contraception
Interventions
DRUG

Levonorgestrel (13,5 mg) intrauterine device

DEVICE

Cooper (380mm2) intrauterine device

Trial Locations (1)

08025

Hospital de la Santa Creu i Sant Pau, Barcelona

Sponsors

Collaborators (1)

Bayer
All Listed Sponsors
collaborator

Bayer

INDUSTRY

lead

Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

OTHER

NCT02957292 - A Study to Compare the Menstrual Bleeding Profile Among Jaydess® and Copper Intrauterine Device (IUD) Users. COLIBRI STUDY (Copper and Levonorgestrel IUD Barcelona Research Initiative). | Biotech Hunter | Biotech Hunter