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the effect of Rosa Damascena Mill on constipation in pregnancy

Phase 2
Recruiting
Conditions
constipation in pregnancy.
constipation
K59.0
Registration Number
IRCT20190427043388N1
Lead Sponsor
Shahed University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
35
Inclusion Criteria

Healthy pregnant women with constipation based on ROME III criteria
Age over 18 and under 45 years
Patient's consent to participation in the study
Pregnancy Week 14-34
Not using of medicine to treatment constipation
The absence of a history of anorectal disease

Exclusion Criteria

Lack of willingness to cooperate
Medicinal sensibility
pregnancy and midwifery problem (ROM, Premature Labour, Placeta abruption, pre eclampsia)
anorectal disease
Use of other medication during treatment
Any problem lead to patient bed

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Constipation score. Timepoint: Before intervention, after 2 weeks, after 4 weeks. Method of measurement: Constipation Questionnaire based on Rome III criteria.;Quality of Life score. Timepoint: Before intervention, after 4 weeks. Method of measurement: WHO Quality of Life Questionnaire.
Secondary Outcome Measures
NameTimeMethod
Rosa Damascena Mill product use frequency. Timepoint: End of week 4. Method of measurement: questionnaire.
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