A clinical trial on Ayurvedic therapy to achieve normal labor
Phase 2
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2021/05/033334
- Lead Sponsor
- ational Institute of Ayurveda
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Pregnantwomenwithcompleted35weeksof
gestational age
2.Agebetween20to40years.
3.Pregnantwomenofheightbetween147-170cm
4.Pregnantwomenofweight45-75kgandHbmorethan
10gm %
Exclusion Criteria
1.Primigravidaeover35yearsofage
2.Grandmultiparaei.e.parity >4
3.PreviousLSCS,Badobstetrichistory,Pregnancy
associatedwithPIH,Chronichypertension,Gestational
diabetes,Rhincompatibility
4.Previouspregnancieswithcomplicationslike
Intrauterinefetaldeath,Postpartumhemorrhage,Ante
partumhemorrhage.
5.WomanwithsystemicillnesslikeBronchialasthma,
HTN,Tuberculosis,Cardiacdisorder
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1)To regularize uterine <br/ ><br> contractions and relaxations to <br/ ><br>bring about sukhaprasavaTimepoint: Improvement in subjective and objective parameters
- Secondary Outcome Measures
Name Time Method 1)To reduce the duration of first and second stage of <br/ ><br>labor <br/ ><br>2)To reduce fetal complications like respiratory distress during and immediately after laborTimepoint: Twice a week after 35 weeks till the onset of labour