Hemorrhoid. Other hemorrhoids
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with grade 1-2 internal hemorrhoids Age 18-65 years Patients with bleeding or hemorrhoidal prolapse or pain or two or all together Have a signed informed consent form to participate in the study
Exclusion criteria
Exclusion criteria: Anorectal diseases such as rectal prolapse, Fisher, fistula, perianal abscess Thrombosis and gangrenous hemorrhoids Uncontrolled cardiovascular disease Cirrhosis Inflammatory bowel disease (IBD) Pregnancy and lactation History of allergy to herbal medicines Use analgesics less than a week ago Use of anticoagulants less than a month ago Use of steroid less than a month ago Unwillingness to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain according to CORECTS questionnaire. Timepoint: At the first (before starting the study), end of the first and the second week. Method of measurement: Colo-Rectal Evaluation of Clinical Therapeutics Scale (CORECTS) questionnaire.;Rectorrhagia according to CORECTS questionnaire. Timepoint: At the fist (before starting the study), end of the first and the second week. Method of measurement: Colo-Rectal Evaluation of Clinical Therapeutics Scale (CORECTS) questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Itching according to CORECTS questionnaire. Timepoint: At the fist (before starting the study), end of the first and the second week. Method of measurement: Colo-Rectal Evaluation of Clinical Therapeutics Scale (CORECTS) questionnaire.;Quality of Life. Timepoint: At the fist (before starting the study), end of the first and the second week. Method of measurement: The World Health Organization Quality of Life Instrument, Short Form (WHOQOL-BREF) questionnaire.;Possible side effects of treatment. Timepoint: At the fist (before starting the study), end of the first and the second week. Method of measurement: Researcher-made questionnaire.;Satisfaction of treatment. Timepoint: At the fist (before starting the study), end of the first and the second week. Method of measurement: Researcher-made questionnaire (according to Visual Analogue Scale). | — |
Countries
Iran (Islamic Republic of)
Contacts
Ardabil University of Medical Sciences