2005
DOI: 10.1093/humrep/dei204
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Misoprostol moistened with acetic acid or saline for second trimester pregnancy termination: a randomized prospective double-blind trial

Abstract: This new regimen of 800 microg of vaginal misoprostol every 6 h for a maximum of three doses in 24 h was an effective alternative method for second trimester abortion. In addition, misoprostol moistened with acetic acid was significantly more effective than misoprostol moistened with saline.

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Cited by 24 publications
(24 citation statements)
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“…The regimens of group B (600 mg every 6 h) and C (800 mg every 12 h) in the present study achieve shorter induction-abortion intervals than was observed in previous studies with the same dosage schedules of misoprostol tablets not moistened with acetic acid [3][4][5][6][12][13][14][15] . Moistening the tablets of misoprostol with acetic acid before vaginal administration increases the abortifacient efficacy.…”
Section: Discussionsupporting
confidence: 61%
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“…The regimens of group B (600 mg every 6 h) and C (800 mg every 12 h) in the present study achieve shorter induction-abortion intervals than was observed in previous studies with the same dosage schedules of misoprostol tablets not moistened with acetic acid [3][4][5][6][12][13][14][15] . Moistening the tablets of misoprostol with acetic acid before vaginal administration increases the abortifacient efficacy.…”
Section: Discussionsupporting
confidence: 61%
“…a Chi-Square test tablets moistened with 3 ml of 5 % acetic acid and (ii) tablets moistened with 3 ml of saline 3 . This study showed that a new regimen of 800 mg of vaginal misoprostol every 6 h for a maximum of three doses in 24 h was effective and that misoprostol moistened with acetic acid was significantly more effective than moistened with saline 3 .…”
Section: Discussionmentioning
confidence: 99%
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“…Other clinical trial results suggest that moistening the misoprostol tablets in acetic acid solution before vaginal insertion optimizes dissolution, as pH values in loco are known to affect the pharmacokinetics of this drug. 70 Another interesting approach for misoprostol delivery has been the use of a vaginal insert similar to the commercially available inserts used for dinoprostone. The major clinical advantages of this system involve the controlled release of misoprostol from the hydrogel polymer contained in the insert, allowing for its gradual absorption into the systemic circulation and a reasonably rapid decrease in plasmatic levels after removal, which makes hyperstimulation controllable and reversible.…”
mentioning
confidence: 99%