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Comparison of Continuous Erector Spinae Block(pain reliving technique) with Continuous Epidural Analgesia (pain reliving technique)

Comparison of Post-operative analgesic efficacy of Continuous erector spinae plane block with Continuous Epidural Analgesia in Renal transplant Recipient surgery- a randomized, open label, non-inferiority trial. - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/064246
Enrollment
70
Registered
2024-03-15
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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 Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Continuous Erector spinae block for postoperative pain managment: Patients will receive Erector spinae block at T10-T11 level with 20g catheter with local anaesthetic for 48 hrs after e

Sponsors

Tapas Kumar Singh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients planned for renal transplant recipient surgery under general anaesthesia

Exclusion criteria

Exclusion criteria: Patient’s refusal, difficult sonoanatomy, BMI greater than 25, inability to understand PCA pump

Design outcomes

Primary

MeasureTime frame
Total IV PCA Fentanyl consumption at 48 hr time pointTimepoint: 48 hr time point after the end of surgery—

Secondary

MeasureTime frame
Time for ambulationTimepoint: after surgery;Amount of Noradrenaline consumed during surgery (in micrograms.Timepoint: during surgery (intraoperatively);Postoperative nausea and vomiting (PONV)Timepoint: 48 hr time point after the end of surgery;Recipient satisfaction with analgesia: YES or No.Timepoint: 48 hr time point after the end of surgery;Static and Dynamic pain scoresTimepoint: 30 mins, 2, 24 and 48 hours after the end of surgery—

Countries

India

Contacts

Public ContactTapas kumar singh

Sanjay Gandhi Postgraduate Institute of Medical Sciences

sandeepsahu09@gmail.com08004904598

Outcome results

None listed

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