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Comparing Two Methods of Pain Control for Putting a Dislocated Shoulder Back in Place: Shoulder block Injections and Intravenous Medicines

Efficacy of Combined Suprascapular and Axillary Nerve Block Compared to Intravenous Procedural Analgesia for Reduction of Anterior Shoulder Dislocation: A Randomized Clinical Trial - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/07/113899
Enrollment
40
Registered
2026-07-13
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: M218- Other specified acquired deformities of limbs

Interventions

Intervention1: combined suprascapular and axillary nerve block: Combined suprascapular and axillary nerve block with 0.75% ropivacaine in shoulder dislocation surgery Control Intervention1: procedural

Sponsors

Uttar Pradesh University of Medical Sciences Saifai Etawah UP
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: The study will be conducted on 1. Adult patients aged from 18 to 60 years old of either sex with a BMI less than 30 2. American Society of Anaesthesiologists physical status I and II and III 3. Planned for closed reduction for anterior shoulder dislocation.

Exclusion criteria

Exclusion criteria: 1. Patients for whom informed consent could not be obtained 2. Patients with systolic blood pressure less than 90 mm Hg or pulse less than 60 per minute 3. Patients with known chronic renal or liver failure 4. Patients are allergic to the medications to be used 5. Patients diagnosed with a fracture, together with the dislocation 6. Polytrauma patients.

Design outcomes

Primary

MeasureTime frame
pain score using VASTimepoint: pain score using VAS at baseline and at 2 hour after the procedure

Secondary

MeasureTime frame
The number of attempts required for successful reductionTimepoint: noted at the end of surgery;hemodynamic adverse eventsTimepoint: throughout the perioperative period noted at the end of surgery;Respiratory adverse eventsTimepoint: throughout the perioperative period noted at the end of surgery;patient satisfaction scoreTimepoint: asked single time at 24 hour after the surgery

Countries

India

Contacts

Public ContactDr Shipra Verma

Uttar Pradesh University of Medical Sciences, Saifai, Etawah, Uttar pradesh

lamhe.17@gmail.com9458657706

Outcome results

None listed

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