IRCT201612278170N10
Completed
Phase 2
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 sites54 target enrollmentTBD
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- hemorrhoid.
- Sponsor
- Vice President of Research Tabriz University Of Medical Sciences
- Enrollment
- 54
- Status
- Completed
- Last Updated
- 8 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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.
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Not specified
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