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Correspondence| Volume 95, ISSUE 4, P434-435, April 2017

Comments on manuscript: vaginal misoprostol prior to intrauterine device insertion in women delivered only by elective cesarean section: a randomized double-blind clinical trial

      We read the manuscript published by Abdellah et al. entitled “Vaginal misoprostol prior to intrauterine device insertion in women delivered exclusively by elective Cesarean section: a randomized double-blind trial” [

      Abdellah MS, Abbasa AM, Hegazy AM, El-Nashara IM. Vaginal misoprostol prior to intrauterine device insertion in women delivered only by elective cesarean section: a randomized double-blind clinical trial. Contraception, 2017;30005-7.

      ] with great interest. In our opinion, this paper contributes valuable information to the literature on the subject of facilitating intrauterine device (IUD) insertion. The strengths of the study include the fact that it was a double-blind randomized clinical trial (RCT), the participants consisted of women who had delivered exclusively by Cesarean and all the IUD insertions were performed by the same professional.
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      References

      1. Abdellah MS, Abbasa AM, Hegazy AM, El-Nashara IM. Vaginal misoprostol prior to intrauterine device insertion in women delivered only by elective cesarean section: a randomized double-blind clinical trial. Contraception, 2017;30005-7.

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