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Comparing the effectiveness of two drugs the control 0.5 percent levobupivacaine and the test 0.75 percent ropivacaine used in ultrasound guided below clavicle nerve block in patients posted for lower arm and forearm surgeries

Comparison of the efficacy of 0.5 percent levobupivacaine versus 0.75 percent ropivacaine in ultrasound guided costoclavicular block for upper limb surgeries - A prospective randomized control study. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/090314
Enrollment
60
Registered
2025-07-07
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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: Drug intervention: Group L- a single injection of 20ml of 0.5% levobupivacine under ultrasound guidance given as a peripheral nerve block with a duration of action up to 6 to 8 hours Co

Sponsors

Dr Diksha Dmello
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age between 18 and 65 years ASA physical status 1 and 2 and 3 Voluntary participation in the trial Surgeries for upper limb below mid shaft of humerus under brachial plexus block

Exclusion criteria

Exclusion criteria: Refusal to participate Local anesthetic allergy Infection at block site Prior infraclavicular fossa surgery Bleeding or evidence of coagulopathy

Design outcomes

Primary

MeasureTime frame
To assess the mean duration of sensory block between the two groups Timepoint: 2, 4, 6, 8, 10 , 12 hours post operatively

Secondary

MeasureTime frame
onset of sensory blockTimepoint: 0, 5, 10, 15, 20, 25 and 30 mins after injection;onset of motor blockTimepoint: 0, 5, 10, 15, 20, 25 and 30 minutes after injection;Duration of motor blockTimepoint: from time of injection to 2, 4, 6, 8, 10 and 12 hours post operatively or upto motor block receeding.;time to first analgesic requirementTimepoint: to be assessed at 2,4,6,8,10 & 12 hours post operatively for pain;Incidence of block failureTimepoint: assessed at 0, 5, 10, 15, 20, 25 up to 30 mins after injection

Countries

India

Contacts

Public ContactDr Diksha Dmello

Manipal Academy of Higher Education

dikshadmello27@gmail.com9591463444

Outcome results

None listed

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