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The effect of Myrtoid suppository in hemerrhoid treatment

Phase 3
Conditions
hemorrhoids.
Unspecified haemorrhoids without complication
Registration Number
IRCT201506211165N7
Lead Sponsor
Baghiatallah University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
100
Inclusion Criteria

All the visited patients with hemorrhoid symptoms who lack the exclusion criteria

Exclusion criteria:

External thrombosed hemorrhoid; Internal strangulated hemorrhoid; Anal fistula; Anal fissure; Anal abscess; Pregnancy; Portal hypertension; Type 3 and 4 hemorrhoids; Renal insufficiency; Malignancies

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Bleeding. Timepoint: Before intervention, 2 weeks after the initial intervention. Method of measurement: questionnaire.;Pain during bowel movements. Timepoint: Before intervention, 2 weeks after the initial intervention. Method of measurement: questionnaire.;Constant pain in anus. Timepoint: Before intervention, 2 weeks after the initial intervention. Method of measurement: questionnaire.;Heaviness in anus. Timepoint: Before intervention, 2 weeks after the initial intervention. Method of measurement: questionnaire.;Tenesmus. Timepoint: Before intervention, 2 weeks after the initial intervention. Method of measurement: questionnaire.;Anal itching. Timepoint: Before intervention, 2 weeks after the initial intervention. Method of measurement: questionnaire.;Irritation in anus. Timepoint: Before intervention, 2 weeks after the initial intervention. Method of measurement: questionnaire.
Secondary Outcome Measures
NameTimeMethod
Adverse effects. Timepoint: during the treatment period. Method of measurement: clinical assessment.
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