A clinical study of Ayurvedic therapy in achieving normal delivery
- Conditions
- Health Condition 1: O629- Abnormality of forces of labor, unspecified
- Registration Number
- CTRI/2020/04/024740
- 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
1.Patient willing and able to participate in study with written informed consent.
2.Pregnant women of age between 20-40 years.
3.Gestational age after 35 weeks.
4.Pregnant women of height 150-170cm.
5.Pregnant women of weight 45-75kg.
6.Hemoglobin more than 10 gm%
1.Primigravidae over 35 years of age.
2.Grand multiparae i.e. parity >4.
3.History of previous LSCS along with Bad obstetric history.
4.Pregnancy associated with Pregnancy induced hypertension, Pre-eclampsia, Eclampsia, Gestational Diabetes, Placenta previa, Abruptio placentae.
5.Patients with Cephalo-pelvic disproportion.
6.Patients with any systemic disorder like Diabetes Mellitus, Renal disorder, Cardiac disorder, Tuberculosis, Bronchial asthma.
7.Patients with pathology of Reproductive system like Uterine or Cervical fibroid, Benign or Malignant tumor , Fothergill repair, Recto vaginal fistula, Vesico vaginal fistula, Ovarian cyst.
8.Past history of complication during previous pregnancy or labor like Abruptio placentae,
Postpartum haemorrhage, Intra uterine fetal death.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Achievement of Sukhprasava (Eutocia).Timepoint: 45 days
- Secondary Outcome Measures
Name Time Method 1. Shortening the duration of stages of labor (Partogram). <br/ ><br> 2. Reduction in the complications of labor <br/ ><br>Timepoint: 45 days