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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03505047
Study type Interventional
Source University of Cape Town
Contact
Status Completed
Phase N/A
Start date May 10, 2018
Completion date January 31, 2020

See also
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