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Immediate Versus Delayed IUD Insertion After Second Trimester Medical Abortion

NCT03505047 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 110

Last updated 2020-03-26

No results posted yet for this study

Summary

The main objective of the study is to compare use, in a randomised controlled trial, of the the copper IUD if inserted immediately after completion of a second trimester medical abortion, to standard care with insertion 3-4 or more weeks after abortion at community health centres.

Conditions

  • Contraception

Interventions

DEVICE

Copper Intrauterine device

Immediate insertion of the copper intrauterine device after completion of abortion

Sponsors & Collaborators

Principal Investigators

  • Deborah Constant, PhD · University of Cape Town

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-05-10
Primary Completion
2019-08-31
Completion
2020-01-31

Countries

  • South Africa

Study Locations

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Entities

Companies

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 NCT03505047 on ClinicalTrials.gov