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Comparison of efficacy of two techniques of brachial plexus block for anesthesia of arm in patients being operated for fracture humerus.

Comparison of efficacy of ultrasound guided continuous Interscalence block vs continuous Costoclavicular Brachial Plexus Block for Humerus Fractures in obese patient. A single center randomized control trial.

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/097419
Enrollment
60
Registered
2025-11-13
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Health Condition 1: M25- Other joint disorder, not elsewhere classified

Interventions

Intervention1: Continuous interscalene brachial plexus block.: All obese patient having humerus fracture will be given continuous interscalne brachial plexus block for the surgerical anesthesia and

Sponsors

Government Institute of Medical Science
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA one, two , three , BMI more than equal to 25Kilogram per meter square having fracture of humerus scheduled for open reduction and internal fixation.

Exclusion criteria

Exclusion criteria: Refusal to participate, BMI less than 25 kiligram per meter square, pre-existing moderate-severe pulmonary disease (obstructive or restrictive), pre-existing neuropathy of the operative limb, coagulopathy, hepatic failure (Child-Turcotte-Pugh score more than 9) or renal failure (creatinine more than 2 milligram per decilitre or peritoneal di alysis or hemodialysis), infection at the puncture site, hypersensi tivity or allergy to LA, pregnancy, inability to communicate or cooperate and patients having chronic pain condition.

Design outcomes

Primary

MeasureTime frame
To compare the efficacy of continuous interscalene block and continuous costoclavicular block in obese patients undergoing surgery for humerus fracture.Timepoint: 0 minute. 15minute,30 minute, 6 hours,12hours,18 hours, 24 hours , 36hours, 48hours.

Secondary

MeasureTime frame
1.Diaphragmatic excursion 2.Patient having any complications like Hoarseness, Dsypnoea Horners syndrome, PONV, Bradycardia ,Hypotension, Incidence of LAST, Pneumothorax 3.Accidental catheter dislodgement.Timepoint: 0 minute. 15minute,30 minute, 6 hours,12hours,18 hours, 24 hours , 36hours, 48hours.

Countries

India

Contacts

Public ContactAnupriya saxena

Government Institute of Medical Science

anupriya.pmch@gmail.com9953090044

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Sep 19, 2026