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Comparison of recovery between patient following enhanced recovery after caesarian delivery and patient treated with normal post caesarian section recovery protocol

Maternal Outcomes Following Elective Caesarean Section:A Randomized Controlled Trial Of ERAS versus Conventional care

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/097347
Enrollment
100
Registered
2025-11-13
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: Z488- Encounter for other specified postprocedural aftercare Health Condition 2: Z488- Encounter for other specified postprocedural aftercare

Interventions

Control Intervention1: conventional arm: Foley’s catheter removed within 24-48 hours of surgery, injectable antibiotics and analgesics continued for 48 hours postoperatively followed by five days oral

Sponsors

K Varshini
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.singleton pregnancy 2.18-45 years of age group 3.more than 28 weeks gestation

Exclusion criteria

Exclusion criteria: 1.Women undergoing emergency cesarean delivery 2.Hypertensive disorders of pregnancy 3.Cardiac diseases, pulmonary diseases 4.Chronic renal diseases 5.Women diagnosed with antepartum hemorrhage Placenta previa, Placenta accreta spectrum 6.Nonconsenting women 7.Patients with hemorrhagic diathesis

Design outcomes

Primary

MeasureTime frame
Primary objective: To assess the effectiveness of the ERAS protocol in reducing post operative recovery time (measured by time to mobilization, time to oral intake, and length of hospital stay) following elective cesarean deliveryTimepoint: More than 28 weeks period of gestation

Secondary

MeasureTime frame
Secondary objectives: 1.To compare the postoperative pain scores (using standardized pain scales such as VAS) between ERAS & standard care groups 2.To evaluate maternal satisfaction with postoperative care 3.To assess the incidence of postoperative complications, including nausea, vomiting, wound infection, & bleeding Timepoint: More than 28 weeks period of gestation

Countries

India

Contacts

Public ContactK Varshini

JNMC, KLE

anitamgan@gmail.com9448140343

Outcome results

None listed

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