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A clinical trial to evaluate the effect of isabgol with pawanmuktasana in postpartum women who underwent episiotomy having constipation.

Not Applicable
Conditions
Health Condition 1: O701- Second degree perineal lacerationduring delivery
Registration Number
CTRI/2020/12/029751
Lead Sponsor
CARC
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Females with vaginal delivery only underwent either episiotomy or secondary perineal tear.

2. Patients who are in sutikakala till first rajodarshan.

3. Diagnosed with constipation.

Exclusion Criteria

1. Excessive swelling, gaping at perineal stitches.

2. Septicemia of wound.

3. Third or fourth degree perineal tear.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improvement in the Constipation Scoring Scale and Bristol Stool Scale.Timepoint: 20 days
Secondary Outcome Measures
NameTimeMethod
To observe any side effects of Isabgol in volunteers.Timepoint: 20 days
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