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Efficacy of ''Malva sylvestrison functional constipation .

Not Applicable
Conditions
constipation.
constipation
Registration Number
IRCT2014031617032N1
Lead Sponsor
Faculty of Traditional Medicines,Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
110
Inclusion Criteria

Men and women aged 18–65 as having at least two or more of the following, during 25% of defecation times: very hard and/or hard stools; sensation of incomplete evacuation; straining at defecation; a need for digital manipulation to facilitate evacuation.These criteria should have been fulfilled for the 3 previous months with symptom onset at least 6 months prior to diagnosis.
Exclusion criteria:Men and women <18 years;Men and women>65 years;patients with mentioned criteria & drug-induced constipation, patients suffering from secondary causes of chronic constipation, including endocrine, metabolic, or neurological disorders; patients with a history of gastrointestinal surgery(exception of appandectomy and cholecystectomy); those with a diagnosis of constipation dominant IBS; Patients with alarming symptoms (fever, recent weight loss , and anaemia)& constipation.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Defecation rate per week on average. Timepoint: before interventing &2,4 weeks aftertreatment. Method of measurement: ROME III questionnaire.;Hard stools. Timepoint: before interventing & 2,4 weeks aftertreatment. Method of measurement: ROME III questionnaire& Bristol stool form scale.;Need for digital manipulation to facilitate evacuation. Timepoint: before interventing & 2,4 weeks aftertreatment. Method of measurement: ROME III questionnaire.;Sensation of blockage. Timepoint: before interventing & 2,4 weeks aftertreatment. Method of measurement: ROME III questionnaire.;Straining of defecation. Timepoint: before interventing & 2,4 weeks aftertreatment. Method of measurement: ROME III questionnaire.
Secondary Outcome Measures
NameTimeMethod
Rarely dyspepcia. Timepoint: every time patient reports. Method of measurement: patient report.
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