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Effect of ayurveda based prasav protocol on normal vaginal delivery and labour outcomes in full term pregnant women

To evaluate the effect of prasav protocol in optimising normal vaginal delivery and labour outcomes: a comparative clinical study with modern birthing practices - nil

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/111589
Enrollment
50
Registered
2026-06-01
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Pt Khushilal Sharma Government Autonomous Ayurveda College and Institute Bhopal 462003
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Full term pregnant women 37 to 40 weeks of gestation Singleton pregnancy with cephalic presentation Height 149 to 172cm Adequate pelvis No prior use of labour inducing agents before enrollment Willing to provide informed consent and participate ICD 10 CM DIGNOSIS CODE O80 Encounter for full term uncomplicated delivery

Exclusion criteria

Exclusion criteria: High risk pregnancies PIH preeclampsia GDM IUGR oligo polyhydramnios placenta previa anaemia Mal presentation Multiple gestation Cephalopelvic disproportion Systemic disorders DM renal cardiac TB coagulopathies Induced augmented labour at admission Benign or malignant reproductive tumors Fistula or pelvic floor disorders Obstetric or medical emergencies History of pelvic uterine surgery Fothergill repair sling surgery myomectomy septal resection

Design outcomes

Primary

MeasureTime frame
Rate of uneventful spontaneous normal vaginal delivery between Prasav Protocol group and modern birthing practice groupTimepoint: Assessed at the completion of delivery (after completion of 3rd stage of labour) by evaluating whether spontaneous vaginal delivery occurred uneventfully

Secondary

MeasureTime frame
Duration/progress of labour- active labour to completion of 3rd stage Intensity of labour pain (VAS scale) Maternal fatigue (Fatigue Severity Scale) Maternal satisfaction regarding birthing experience Postpartum mental state (EPDS score) Requirement of obstetric or medical interventions Bishops score improvement Neonatal outcome (APGAR score at 1 and 5 minutes) Incidence of postpartum hemorrhage Postpartum infection rateTimepoint: At admission before active labour Bishop s score assessment During different phases of labour Labour pain assessment VAS From onset of active labour till completion of 3rd stage of labour Progress and duration of labour Throughout labour and delivery Requirement of medical obstetric interventions Immediately after delivery completion of 3rd stage Primary outcome spontaneous vaginal delivery rate PPH assessment Within 24 hours postpartum Maternal fatigue maternal satisfaction EPDS assessment After 24 hours postpartum Postpartum infection assessment At 1 minute after birth APGAR score At 5 minutes after birth APGAR score

Countries

India

Contacts

Public ContactDr Ankita Raval

Pt Khushilal Sharma Government Autonomous Ayurveda College and Institute Bhopal 462003

basantiayu75@gmail.com9827579276

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026