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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
110
Immediate insertion of the copper intrauterine device after completion of abortion
Groote Schuur Hospital
Cape Town, Western Province, South Africa
Use of the copper IUD
Number of women using the IUD
Time frame: 6 weeks after second trimester abortion
Insertion of the IUD
Number of IUD insertions
Time frame: 6 weeks after second trimester abortion
Use of the IUD at 3 months post-abortion
Number of women using the IUD
Time frame: 3 months after second trimester medical abortion
Use of the IUD at 6 months post-abortion
Number of women using the IUD
Time frame: 6 months after second trimester medical abortion
Spontaneous expulsion of the IUD
Number of full and partial expulsions
Time frame: 6 weeks post-abortion
Spontaneous expulsion of the IUD
Number of full and partial expulsions
Time frame: Between 6 weeks and 3 months post abortion
Spontaneous expulsion of the IUD
Number of full and partial expulsions
Time frame: Between 3 and 6 months post abortion
Removal of IUD and associated factors
Number of removals
Time frame: within 3 and 6 months post-abortion
Abortion-related and IUD-related complications
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Number of complications
Time frame: within 3 months post-abortion
Women's satisfaction and acceptability of the IUD
5 point scales
Time frame: Reported at 3 and 6 months post-abortion
Recurrent pregnancy
Number of recurrent pregnancies
Time frame: At 6 months post-abortion