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A Study to comapre two regional anesthesia technique for pain relief in Proximal Humerus Fracture Surgeries

A randomized comparative trial on evaluation of cervical erector spina plane block versus interscalene brachial plexus blocks for proximal humerus fracture surgeries. - NIL

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/086467
Enrollment
50
Registered
2025-05-07
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: S422- Fracture of upper end of humerus

Interventions

Intervention1: interscalene brachial plexus block: Interscalene block will be given under ultrasound guidance once before incision Control Intervention1: cervical erector spina plane block: cervical e

Sponsors

Sancheti Institute of Orthopedics and Rehabilitation
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All adult patients (18 years and over) scheduled for fracture proximal humerus repair using a nerve block as part of their anesthetic care

Exclusion criteria

Exclusion criteria: 1. Patients who refused to participate in the study. 2. Patients with a history of cardiac, renal, or hepatic disease. 3. Patients with pre-existing neurologic deficits or neuropathy affecting the brachial plexus. 4. Patients with contraindications to peripheral nerve block. 5. Patients with known allergies to local anesthetic drugs.

Design outcomes

Primary

MeasureTime frame
1.Incidence of diaphragmatic paresis or paralysis assessed as change in the diaphragmatic excursion (measured bilaterally using ultrasonography)Timepoint: Once After shifting to PACU.

Secondary

MeasureTime frame
1. time to first analgesic 2. pain scores 3. intraoperative fentanyl consumption 4. Postoperative opioid use 5. overall satisfactionTimepoint: 1. time to first analgesic: in the postoperative period 2. pain scores: tim3 0,1 ,4, 8 ,24 hours 3. intraoperative fentanyl consumption during surgery 4. Postoperative opioid use in first 24 hopurs 5. overall satisfaction at 24 hours

Countries

India

Contacts

Public ContactDr Sandeep Diwan

Sanchti Institute of Orthopedics and Rehabilitation

sdiwan1965@gmx.com8484914584

Outcome results

None listed

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