NCT02167763View on ClinicalTrials.gov

Comparative Study of the VeraCept Low-Dose Intrauterine Copper Contraceptive vs. the TCu380 Copper IUD

PHASE1CompletedINTERVENTIONAL

Enrollment

300

Participants

Timeline

Start Date

November 30, 2013

Primary Completion Date

December 31, 2014

Study Completion Date

December 31, 2017

Conditions

Prevention of Pregnancy

Interventions

DEVICE

VeraCept Intrauterine Copper Contraceptive

DEVICE

TCu380 IUD

Trial Locations (1)

Unknown

Clinica Canela, La Romana

All Listed Sponsors

lead

Sebela Women's Health Inc.

INDUSTRY

NCT02167763 - Comparative Study of the VeraCept Low-Dose Intrauterine Copper Contraceptive vs. the TCu380 Copper IUD | Biotech Hunter | Biotech Hunter