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A clinical trial to comparatively evaluate the analgesic efficacy of ultrasound guided erector spinae plane block versus wound site infiltration in patients undergoing open nephrectomy.

Ultrasound guided erector spinae plane block versus wound site infiltration for postoperative analgesia in patients undergoing open nephrectomy - Nil

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/062847
Enrollment
44
Registered
2024-02-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: N19- Unspecified kidney failure

Interventions

Intervention1: Ultrasound guided erector apinae plane block: Patients in group A will recieve 30ml of 0.2% ropivacaine after induction of general anaesthesia. Control Intervention1: Wound site infiltr

Sponsors

Dayanand Medical college and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients of 18-75 years of age, American Society of Anaesthesiologists (ASA) I-III undergoing open nephrectomy with flank incision

Exclusion criteria

Exclusion criteria: 1. Patients allergic to local anaesthetics being used 2. Infection at the site of infiltration of local anaesthetic 3. Patients with uncontrolled bleeding diathesis evidenced by history and laboratory investigations 4. Patients with Psychiatric disorder 5. Patients unable to comprehend VAS score 6. Patients with chronic opioid abuse 7. Refusal to participate in the study

Design outcomes

Primary

MeasureTime frame
To evaluate the analgesic efficacy of ESPB and wound site infiltration in open nephrectomy patients in post operative period.Timepoint: Comparative consumption of the total amount of rescue opioid analgesic in a 24 hour period among both the groups will be noted and bidirectional Visual Analogue Scale(VAS) will be recorded at rest and on movement preoperatively i.e prior to block administration before induction of general anesthesia and then postoperatively every hourly for the first 4 hours, 2 hourly for next 2 hours and 4 hourly till 24 hours.

Secondary

MeasureTime frame
Duration of analgesia and Quality of revovery questionnareTimepoint: Quality of recovery questionnare at 24 hours postoperatively

Countries

India

Contacts

Public ContactDr Inayat Jearth

Dayanand Medical College and Hospital

inayat.jearth80@gmail.com9815855260

Outcome results

None listed

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