Misoprostol for nulliparous women did not decrease pain or improve the ease of insertion of an IUD. Most women were willing to wait for a medication that decreases pain, indicating a need to pursue alternatives for pain control with IUD insertion....
Objective: The aim of the study was to assess whether vaginal administration of misoprostol before copper intrauterine device (IUD) insertion increased the success of the procedure among parous women with previous insertion failure. Methods: A single-centre, parallel-group, double-blind, placebo-...
Independent of parity, participants who had heard of the IUD from a health care provider were 2.7 times more likely to be interested in using the method. The study population was at high risk for sexually transmitted infections (STIs); however, 82% of participants predicted that they would ...
Benefits of vaginal misoprostol prior to IUD insertion in women with previous caesarean delivery: a randomised controlled trialObjective: The aim of the study was to evaluate thMagedBeniAhmedBeniM.BeniYoussefBeniGamalBeniEldalyBeniAshrafBeniOmran
Caesarean sectionintrauterine devicemisoprostolpainObjective: The aim of the study was to evaluate the value of vaginal misoprostol 6h prior to intrauterine device (IUD) insertion in women with previous Caesarean delivery.Maged, Ahmed M.Youssef, GamalEldaly, AshrafOmran, EmanEl Naggar, MohamedHak, ...
SUMMARY ANSWER The use of misoprostol at a dose of 400 碌g administered vaginally 4 h prior to IUD insertion increased the ease of insertion and reduced the incidence of pain during the procedure, although the frequency of cramps increased following misoprostol use. WHAT IS KNOWN AND WHAT THIS...
O387 DOES MISOPROSTOL EASE IUD INSERTION IN NULLIPAROUS WOMEN?The aim of this study was to determine current contraceptive use, contraceptive desires and knowledge, future fertility desires, and sterilization regret in a cohort of HIV-positive women. 127 HIV-positive women receiving care at an ...
placebo prior to IUD insertion in nulliparous women that include the stated entry criteria as well as the primary and secondary outcomes listed above will be eligible for inclusion in this PMA as long as the results of any of the included studies are not known to anyone outside the ...
was done using numerical rating scale recorded by the woman and VAS recorded by the health provider; the higher reading of both scales for each case was recorded and analyzed there was no statistical significant difference as regard pain reduction in using misoprostol prior to IUD insertion. As...
(including misoprostol dose, route and timing of administration, the comparator group details, and type of IUD inserted), primary and secondary outcomes of the trial ( including pain score, easiness of insertion score, the need for analgesics, the need for additional measures as cervical dilatation...