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Study about faster recovery after cesarean delivery to improve mother's health and reduce hospital stay.

A Randomized Controlled Trial on the Implementation of Enhanced Recovery After Cesarean (ERAC) Protocol: Impact on Maternal Clinical Outcomes and Length of Hospital Stay. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/102720
Enrollment
200
Registered
2026-02-02
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Intervention1: Enhanced Recovery After Cesarean Protocol: Preop, intraop and postop interventions as per ERAC guidelines Intervention2: Preoperative day: Counselling about ERAC and postoperative recov

Sponsors

Maharana Bhupal Government Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: women aged 18-45 years with singleton pregnancy scheduled for elective cesarean section

Exclusion criteria

Exclusion criteria: Multifetal pregnancies Significant comorbidities like uncontrolled diabates, severe hypertension, preeclampsia, eclampsia

Design outcomes

Primary

MeasureTime frame
duration of length of hospital stay and maternal outcomesTimepoint: postop day—

Secondary

MeasureTime frame
postoperative pain (VAS) scoreTimepoint: At 6, 12, 24 & 48 hours postoperatively;time to ambulationTimepoint: continuously recorded assessed at 6 12 & 24 hours post surgery;initiation of time of breastfeedingTimepoint: time of first successful breastfeeding within 24 hours;maternal satisfactionTimepoint: 48 hours postoperatively & at discharge—

Countries

India

Contacts

Public ContactDr Vanshika Shrivastava

R.N.T Medical College

savitriverma1997@gmail.com9414736507

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026