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Impact of modified versus traditional early recovery after surgery on new kidney graft outcomes following kidney transplant

The effect of modified versus conventional ERAS on clinical and graft outcomes in kidney transplant recipients: A randomised controlled trial - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/065091
Enrollment
70
Registered
2024-04-02
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

Health Condition 1: N186- End stage renal disease

Interventions

Intervention1: Group A: Modified ERAS: Minimal incision + ICE bag technique + TAP block catheter (ropivacaine TID) with or without PCA- fentanyl infusion Control Intervention1: Group B: Conventional

Sponsors

AIIMS NEW DELHI
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • 18 years to 70 years • Both genders • Live donor kidney transplant

Exclusion criteria

Exclusion criteria: • Patients less than 18 years and more than 70 years • Patient refusal to participate in the study • Pregnant or lactating mother • patients with allergy to local anaesthetic drugs • Extended criteria live donors (donor age more than 60 years or donor age more than 50 years with at least two comorbidities) • Deceased donor transplant • Combined liver – kidney or kidney – pancreas transplant. • Follow-up of less than 3 months after kidney transplant

Design outcomes

Primary

MeasureTime frame
1. Clinical and graft outcome scoreTimepoint: up to 7 days

Secondary

MeasureTime frame
1. Length of hospital stay 2. Time to first oral intake 3. Time to return of activity 4. Pain score (VAS) 5. Post-operative opioid consumption days 6. Postoperative complications (vascular, urological, and graft parenchymal) 7. Readmission rates 8. Cost-analysis: Hospital stay charges, hemodialysis sessions, interventional radiology procedures, blood tests, trough levels, biopsy charges etc. Timepoint: 1. days to weeks 2. up to 7 days 3. up to 7 days 4. VAS score 5. up to 7 days 6. up to 3 months 7. up to 3 months 8. In Rupees

Countries

India

Contacts

Public ContactDr Pritee Trivedee

All India Institute of Medical Sciences New Delhi

tpritee12@gmail.com9717628127

Outcome results

None listed

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