Publication: Can vaginal misoprostol effectively increase rate of a satisfactory colposcopy? A randomized double-blind placebo-controlled trial
dc.contributor.author | Duangmani Thanapprapasr | en_US |
dc.contributor.author | Sarikapan Wilailak | en_US |
dc.contributor.author | Nathpong Israngura Na Ayudhya | en_US |
dc.contributor.author | Arb Aroon Lertkhachonsuk | en_US |
dc.contributor.author | Puchong Likittanasombut | en_US |
dc.contributor.author | Suwicha Chittithaworn | en_US |
dc.contributor.author | Chuenkamon Charakorn | en_US |
dc.contributor.author | Sawaek Weerakiet | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.date.accessioned | 2018-09-13T06:21:33Z | |
dc.date.available | 2018-09-13T06:21:33Z | |
dc.date.issued | 2009-10-29 | en_US |
dc.description.abstract | Objective: To evaluate the effectiveness of vaginal misoprostol in overcoming an unsatisfactory colposcopy in the patients who had abnormal cervical cytology and to evaluate side effects of vaginal misoprostol. Methods: Sixty patients with an unsatisfactory colposcopy during the period of September 2007-November 2008 were recruited and randomly allocated to receive either two tablets of 200 μg misoprostol (400 mg) or two tablets of similar-looking placebo vaginally. Colposcopic re-examination was performed ~6 h later. The results and side effects before and 2 weeks after the colposcopic re-examination were recorded. Results: Six out of 30 patients in the misoprostol group (20.0%) had a satisfactory colposcopic re-examination compared with 2 out of 27 patients (7.4%) in the placebo group without statistically significant difference (P = 0.172). Three patients in the placebo group dropped out due to not present at the appointment time. Six out of 30 patients (20.0%) and 1 out of 30 patients (3.3%) in the misoprostol group had side effects before and 2 weeks after the colposcopic re-examination orderly. Twenty-seven patients in the placebo group did not have any side effects before and 2 weeks after the colposcopic re-examination. All side effects occurred were minimal and well tolerated. Conclusions: Four hundred micrograms of vaginal misoprostol were not proved to be effective in converting an unsatisfactory to a satisfactory colposcopy. © The Author (2009). Published by Oxford University Press. All rights reserved. | en_US |
dc.identifier.citation | Japanese Journal of Clinical Oncology. Vol.40, No.3 (2009), 203-207 | en_US |
dc.identifier.doi | 10.1093/jjco/hyp140 | en_US |
dc.identifier.issn | 14653621 | en_US |
dc.identifier.issn | 03682811 | en_US |
dc.identifier.other | 2-s2.0-77950348737 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/27130 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77950348737&origin=inward | en_US |
dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
dc.subject | Medicine | en_US |
dc.title | Can vaginal misoprostol effectively increase rate of a satisfactory colposcopy? A randomized double-blind placebo-controlled trial | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77950348737&origin=inward | en_US |