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To study the advantages of local anaesthetic drug levobupivacaine alone with or addition of other drugs

A comparision of effects of Levobupivacaine with and without adjuvants in supraclavicular brachial plexus block.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/06/034424
Enrollment
60
Registered
2021-06-28
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: - Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Randomised prospective double blinded trial: Patients will be randomly allocated into 3 groups by a computer generated randomised table. Group L- patient receives 25ml of 0.5% plain le

Sponsors

Dr Shwetha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients posted for upper limb (elbow or forearm) orthopedic surgery under brachial plexus block.

Exclusion criteria

Exclusion criteria: Patient refusal, history of allergy to the study drugs, seizure disorder, pre-existing neurological deficits, on anticoagulation.

Design outcomes

Primary

MeasureTime frame
The primary outcome is to assess the block characterisctics of 0.5% Levobupivacaine and 0.5% Levobupivacaine with additives in Ultrasound guided supraclavicular brachial plexus block. to evaluate duration of analgesia , onset of sensory and motor blockade, sedation score. The additives used in our trial are buprenorphine or nalbuphine.Timepoint: Intraoperatively post block for 30 min and post surgery duration of block—

Secondary

MeasureTime frame
Not applicableTimepoint: Not applicable—

Countries

India

Contacts

Public ContactDR SHWETHA

Kasturba Medical College, Manipal Academy of Higher Education (MAHE), Manipal

shajimanipal@yahoo.co.in6360834412

Outcome results

None listed

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