Comparison of the effect of topical ointment Myrtus Communis and anti-hemorrhoid on first and second grade hemorrhoid symptoms and the quality of life of women in post delivery period: a triple-blind controlled clinical trial

Vice President of Research Tabriz University Of Medical Sciences0 个研究点目标入组 54 人开始时间: 待定最近更新: 2018年2月22日

适应症

试验速览

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•Women have given birth for at least 4 weeks and up to 4 months from their delivery, either in the normal way of any cesarean section (including Nully Par and Multipar); women in post delivery period who have been diagnosed their hemorrhoids first and second degree with clinical symptoms and confirmed by the Surgeon General; women between 18-40 years; Women in the postpartum period whose hemorrhoids are not caused by systemic diseases such as hypertension; hemorrhoid symptomsfor at least more than 7 days; The ability to read and write.
•Exclusion criteria: Use of Systemic steroid Drugs and non-steroidal anti-inflammatory drugs and analgesics and anti-hemorrhoid treatments (for a one month prior to the study) and the use of anticoagulant drugs; require surgical procedure for the treatment of hemorrhoids (a gastroenterologist confirmed by clinical testing and colonoscopy); women with problems such as abscesses, anorectal, fistula, tuberculosis, herpes, varicella, fungal infection (confirmed by clinical trials or colonoscopy); risk of gastrointestinal tract infectious inflammatory diseases or colorectal cancer (as the patient); The previous use of laser or the use of medication felebotonic to treat hemorrhoids a week before the study (as the patient); Delivery with vacuums or forceps and delivery of cesarean section with large ancision; the company in another intervention study.

发起方

Vice President of Research Tabriz University Of Medical Sciences