ormal Delivery through Ayurveda

Phase 2

Conditions: Health Condition 1: O80- Encounter for full-term uncomplicated delivery

Registration Number: CTRI/2023/06/053883

Lead Sponsor: ational Institute of Ayurveda Deemed to be university

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: ot Yet Recruiting

Sex: Not specified

Target Recruitment: 0

Inclusion Criteria

1. Patient with37 weeks of gestation with cephalic presentation.

2. Height 148 cm to 172 cm.

3. Haemoglobin more than or equal to 10 gm%.

4. Borderline or adequate pelvis

Exclusion Criteria

1. History of previous LSCS less than or equal to 3 years.

2. Patient having bad obstetric history, precious pregnancy.

3. Pregnancy associated with severe Pregnancy induced hypertension, pre-eclampsia, eclampsia, gestational diabetes, placenta previa (2nd grade posterior, 3rd and 4th grade), abruptio placentae, severe oligohydramnios, severe polyhydramnios, severe IUGR.

4. Patients with cephalo-pelvic disproportion, malpresentation.

5. Patients suffering with systemic disorders like diabetes mellitus, renal dysfunction, cardiac disorder, tuberculosis, coagulopathies.

6. Patients diagnosed with benign or malignant tumor of reproductive system, recto vaginal fistula, vesico-vaginal fistul, second and third degree uterine prolapse.

7. History of fothergill repair, recto vaginal fistula, vesico-vaginal fistul.

8. VDRL, HIV, HBsAg positive pregnant woman.

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Sukhaprasava (Normal Vaginal Delivery)Timepoint: 45 days

Secondary Outcome Measures

Name	Time	Method
Differences in the incidence of complications of all four stages of labor andup to 10 days postpartum between the groups <br/ ><br>Differences in the rate of Sukhaprasava (Eutocia) &Shalyajanana (Caesarean section) between the groups <br/ ><br>Difference in the incidence of fetal distress between the groupsTimepoint: 45 days