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A clinical study to see the effect of Basti and Yonipichu on Progress of Labor.

Phase 3
Conditions
Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Registration Number
CTRI/2023/05/053010
Lead Sponsor
RGGPG Ayurvedic College
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Subject(Pregnant women ) who will give consent for trial.

Primigravida, Primipara and Multigravida

Normal range of haematological/routine ANC investigation

Subject having gynecoid pelvis,borderline pelvis and cephalic presentation

Mild preeclampsia

Exclusion Criteria

Subject(Pregnant Women)not willing to trial

Multipara

CPD

Subject (Pregnant women)having mal-presentation

APH

Subject(Pregnant women) having Hb less than 8gm%

Moderate to severe Pre-eclampsia

Subject (Pregnant women )having any associated gynaecological conditions or systemic disease

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Spontaneous onset of labor and normal Progress of laborTimepoint: 34 weeks of gestation to till delivery
Secondary Outcome Measures
NameTimeMethod
The Clinical result will be assessed by observing the progress of Labor <br/ ><br>Any associated Complaints during trial period will be recordedTimepoint: From 34 weeks of gestation till delivery <br/ ><br>
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