Unlabelled: Topical application of the calcium antagonist nifedipine has demonstrated effectiveness in treating chronic anal fissure, without adverse effects. Like chronic anal fissure, vulvodynia is associated with muscle hypertonicity and an inflammatory infiltrate. We conducted a double-blind placebo-controlled study to investigate the effectiveness of 2 concentrations of topical nifedipine cream in the treatment of vulvodynia. Thirty participants were alternately assigned to 3 topical treatment groups: .2% nifedipine, .4% nifedipine, and placebo. All administered the cream to the vestibule 4 times daily for 6 weeks. For all 3 treatment groups, mean pain intensity on vestibular touch, assessed by the Q-tipped cotton test, pain from speculum insertion, and reports of pain during sexual intercourse was reduced at post-treatment compared with pre-treatment. These improvements remained at 3 months' follow-up. The effectiveness of nifedipine in treating vulvodynia did not exceed that of placebo.

Perspective: The topical application of both nifedipine and a placebo reduced pain in women with vulvodynia. This study highlights the need for controlled trials of treatments for vulvodynia and raises doubts about studies conducted without comparison to placebo.

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http://dx.doi.org/10.1016/j.jpain.2010.03.016DOI Listing

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Article Synopsis
  • The study analyzed data from 8632 patients aged 18 and older with anal fissures (AF) from an Italian health database, focusing on their management and treatment between July 2016 and June 2021.
  • Only 14% of patients received a combination topical treatment of nifedipine and lidocaine (NIF/LID) at the time of their first AF record, highlighting low treatment rates despite increasing healthcare resource use during follow-up.
  • Findings indicated that younger patients were more likely to receive NIF/LID and that there is a significant gap between recommended treatment guidelines and actual management practices, suggesting a need for educational campaigns about anal health in primary care.
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Objective: This study aimed to investigate the efficacy of micronized purified flavonoid fraction in preventing complications after elective hemorrhoidectomy.

Design: Prospective unicentral open-label randomized controlled trial.

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