Skip to content

A study to assess post operative pain in a patient of kidney transplant recipient

Comparison of epidural infusion versus continuous erector spinae plane block for post operative analgesia in patients undergoing renal transplant - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/054808
Enrollment
52
Registered
2023-07-05
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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: Erector Spinae plane block: Erector Spinae plane block is given at T8-T12 spinous process and continuous infusion with Inj. Bupivacaine 0.125% at the rate of 0.1ml/kg/hr till 48hrs post

Sponsors

Post Graduate Institute of Medical Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patient undergoing kidney transplant surgery (living donor and cadaveric) aged 18-65 years

Exclusion criteria

Exclusion criteria: Patient who refuse to give consent Patient with coagulation disorders Patient with opioid addiction Patient who are allergic to local anesthetics Patient with known psychiatric or mental problems Patient having local infection of the skin where block is to be given

Design outcomes

Primary

MeasureTime frame
To compare VNRS scores 24 hours post operatively at rest, between continuous erector spinae plane block (CESPB) and continuous epidural infusion (CEI) groupsTimepoint: To compare VNRS scores 24 hours post operatively at rest, between continuous erector spinae plane block (CESPB) and continuous epidural infusion (CEI) groups

Secondary

MeasureTime frame
(1) To measure pain (VNRS score) at 0 (extubation), 4, 8,12,24,48 hours after surgery during rest and coughing/movement (2) Intraoperative fentanyl consumption (3) 48hours rescue analgesia consumption (4) incidence of hypotension (MAP 20% of baseline) (5) Duration of hospital stay (6) Patient satisfaction score (7) Incidence of complication such as Post operative nausea and vomiting, respiratory depression, bradycardia, Local anesthetic toxicity (LAST)Timepoint: (1) To measure pain (VNRS score) at 0 (extubation), 4, 8,12,24,48 hours after surgery during rest and coughing/movement (2) Intraoperative fentanyl consumption (3) 48hours rescue analgesia consumption (4) incidence of hypotension (MAP 20% of baseline) (5) Duration of hospital stay (6) Patient satisfaction score (7) Incidence of complication such as Post operative nausea and vomiting, respiratory depression, bradycardia, Local anesthetic toxicity (LAST)

Countries

India

Contacts

Public ContactDr Sameer Sethi

Post Graduate Institute of Medical Education and Research

sameersethi29@gmail.com9317851002

Outcome results

None listed

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