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To compare efficacy of levobupivacaine alone or alongwith lignocaine with adrenaline in ultrasound guided supraclavicular block for upper limb surgeries in reducing pain and quality of recovery afterwards.

Comparison of Perioperative Analgesic Efficacy and Quality of recovery on addition of lignocaine with adrenaline to Levobupivacaine in Ultrasound Guided Supraclavicular Block for Upper Limb Orthopaedic Surgeries: A Randomised Control Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/050744
Enrollment
80
Registered
2023-03-15
Start date
Unknown
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Health Condition 1: S424- Fracture of lower end of humerus Health Condition 2: S525- Fracture of lower end of radius Health Condition 3: S526- Fracture of lower end of ulna Health Condition 4: S523- Fracture of shaft of radius Health Condition 5: S522- Fracture of shaft of ulna Health Condition 6: S521- Fracture of upper end of radius Health Condition 7: S520- Fracture of upper end of ulna Health Condition 8: S529- Unspecified fracture of forearm

Interventions

Intervention1: Levobupivacaine and lignocaine with adrenaline: Supraclavicular block given using 14 ml of Levobupivacaine (0.5%), 14 ml of lignocaine with adrenaline and 2 ml of normal saline Control

Sponsors

Government medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA I , II, III

Exclusion criteria

Exclusion criteria: Infection at local sites, hypersensitivity to Local Anaesthetic drugs, per existing neuropathy, bleeding disorders,pregnancy, any hepatic , renal,neurological,psychiatric or neuromuscular diseases.

Design outcomes

Primary

MeasureTime frame
1 To measure first rescue analgesia 2 to measure total analgesic requirementTimepoint: 1) time at which first rescue analgesia given will be recorded. 2) total analgesia required in 24 hours.—

Secondary

MeasureTime frame
1)to compare QoR score in both groups. 2) to blockade characteristics 3) conversion rate to general anaesthesia. 4) peri operative hemodynamic and side effects.Timepoint: 1) QoR-15 score to be compared after 24 hrs of blockade. 2)sensory and motor blockade will be assessed every 1 min for 15 mins. 3)patient complaining of pain in any one nerve distribution even after 30 mins of administration of block. 4)Vital monitoring and side effect will noted every 5 mins for 40 mins And thereafter every 10 mins for 90 mins. Post operative monitoring will be done hrly for 6 hrs and then at 8hr, 12hr, 18hr and 24hr interval.—

Countries

India

Contacts

Public ContactJyoti

BPS GMC Khanpur

meenu297@yahoo.com9467823780

Outcome results

None listed

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