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Decreasing the duration of stay in hospital after caesarean delivery by using early discharge guidelines.

Comparing the enhanced recovery after caesarean delivery with conventional care in maternal outcome: A randomised controlled study. - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/065365
Enrollment
140
Registered
2024-04-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

None listed

Interventions

Intervention1: Caesarean delivery-Conventional care: PRE-OP-NBM more than 8 hours, patient may be counselled, IV fluids may be started, antibiotics may be given. INTRA-OP: No prophylactic vasopressors

Sponsors

S Nijalingappa medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1] Age group :21-45 years women having gestational age more than 37 weeks 2] Elective caesarean deliveries done under Spinal Anaesthesia 3] ASA (American Society Of Anaesthesiologists) physical status II

Exclusion criteria

Exclusion criteria: 1] Refusal to Enroll for the study 2] Any contraindications for spinal anaesthesia 3] Multiple gestation 4] Hypertensive disorders of pregnancy 5] Uncontrolled diabetes mellitus 6] Obesity BMI more than 40kg/m2 7] Other obstetric complications during surgery like post-partum hemorrhage, bladder injury, bowel injury [will be excluded from the study] 8] Any other medical illness like anemia, cardiac diseases, renal diseases

Design outcomes

Primary

MeasureTime frame
Decreased length of stay and early discharge.Timepoint: 72 hours

Secondary

MeasureTime frame
Better maternal satisfaction and maternal bonding with the baby. It also helps in decreasing the burden on maternal socioeconomic status and health care system.Timepoint: 72 hours

Countries

India

Contacts

Public ContactDr Harshitha G

S NIjalingappa Medical college

rameshkoppaldr@gmail.com9845504515

Outcome results

None listed

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