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A Study on the Safety and Efficacy of the SCu300A IUB Compared to the TCu380 Copper IUD

NCT02036203 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2018-07-06

No results posted yet for this study

Summary

This study aims to evaluate the safety and efficacy of the IUB SCu300A spherical copper IUD compared to the standard T shaped copper IUD, the TCu380.

Participants will be followed for one year and quality of life measurements will be measured during this period as well.

Conditions

  • Reversible Prevention of Pregnancy

Interventions

DEVICE

SCu300A IUB

Spherical copper contraceptive

DEVICE

TCu380A IUD

T-shaped copper IUD

Sponsors & Collaborators

  • Ocon Medical Ltd.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
25 Years
Max Age
42 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-01-14
Primary Completion
2014-01-14
Completion
2014-01-14

Countries

  • Israel

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02036203 on ClinicalTrials.gov