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This study compares two methods of pain relief at the area from where skin is taken for a skin graft

Comparison of USG guided femoral plus lateral femoral cutaneous nerve block versus bupivacaine soaked dressing for donor site analgesia in patients undergoing split skin grafting - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/113043
Enrollment
70
Registered
2026-06-19
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: USG guided femoral plus lateral femoral cutaneous nerve block: USG Guided Femoral and Lateral Femoral Cutaneous nerve block with 20 ml 0.25% bupivacaine will be performed on the lower l

Sponsors

Pandit BD Sharma, PGIMS Rohtak
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 70 patients of 18-60 years of age, of either sex, American society of Anaesthesiologists physical status I and II, scheduled to undergo split skin grafting with graft size between 100cm2 - 200cm2 under general anaesthesia will be enrolled for this study

Exclusion criteria

Exclusion criteria: Unwillingness to participate in this study Known hypersensitivity or allergy to local anaesthetics Pre-existing bleeding disorders Infection at the site of the block Pre-existing peripheral neuropathy

Design outcomes

Primary

MeasureTime frame
Pain assessment will be done by a junior resident who will be blinded to the groups, using VAS where 0 denotes no pain and 10 denotes intolerable pain.Timepoint: 30min, 1hr, 2hr, 6hr, 12hr, 24hr—

Secondary

MeasureTime frame
Patient satisfaction wil be assessed via the Likert scale based questionnaire.Timepoint: 30min, 1hr, 2hr, 6hr, 12hr, 24hr—

Countries

India

Contacts

Public ContactDr Ashutosh Tripathi

Pandit BD Sharma, PGIMS Rohtak

ashutoshtripathi199@gmail.com9638506093

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026