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Normal Delivery through Ayurveda

A Randomized comparative clinical trial to evaluate the efficacy of Integrated and Ayurvedic protocol in achieving Sukhaprasava. - nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088264
Enrollment
60
Registered
2025-06-04
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Interventions

None listed

Sponsors

National Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient with 37th week of gestation with singleton pregnancy & cephalic presentation Patient between age of 21 to 40 years Height - 4feet 10inch to 5feet 8inch (148 to 172cm) Hemoglobin more than or equal to 10gm percentage Patient with borderline or adequate pelvis

Exclusion criteria

Exclusion criteria: History of previous LSCS Patient having Bad obstetric history, precious pregnancy Pregnancy associated with severe Pregnancy induced hypertension, Pre-eclampsia, Eclampsia, Gestational Diabetes, Placenta previa, Abruptio placentae, severe oligohydramnios, severe polyhydramnios, severe IUGR Patients with Cephalo-pelvic disproportion, malpresentation. Patients suffering with systemic disorders like Diabetes Mellitus, Renal dysfunction, Cardiac disorder, Tuberculosis, Coagulopathies. Patients diagnosed with Benign or Malignant tumor of Reproductive system, Recto vaginal fistula, Vesico-vaginal fistula, second and third degree uterine prolapse History of Fothergill repair, Recto vaginal fistula, Vesico-vaginal fistula VDRL, HIV, HBsAg positive pregnant woman.

Design outcomes

Primary

MeasureTime frame
Sukhaprasava (Normal Vaginal Delivery)Timepoint: 45 days

Secondary

MeasureTime frame
Difference in the incidence of complications of all four stages of labor and up to 10 days postpartum between the groups. Difference in the rate of Sukhaprasava (Eutocia) & Shalyajanana (Caesarean section) between the groups Difference in the incidence of fetal distress between the groups. Timepoint: 45 days

Countries

India

Contacts

Public ContactDr Kameshwari Panchal

National Institute of Ayurveda

pushpalathania@gmail.com9413206790

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026