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Ultrasound guided Suprascapular nerve block compared with intravenous fentanyl for analgesia in patients with traumatic scapular fractures: An open label prospective randomized controlled trial

Ultrasound guided Suprascapular nerve block compared with intravenous fentanyl for analgesia in patients with traumatic scapular fractures: An open label prospective randomized controlled trial - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/080294
Enrollment
60
Registered
2025-02-10
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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 Health Condition 2: T07- Unspecified multiple injuries

Interventions

Intervention1: Ultrasound Guided Suprascapular Nerve Block: Dose and agent used:2-5 ml of Lignocaine 2% used Frequency: stat dose Route of administration: local infiltration Total duration of obse

Sponsors

Dr Sanjeev Bhoi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: adults traumatic scapular fractures high pain score greater than seven on DVPRS giving valid consent

Exclusion criteria

Exclusion criteria: patients less than eighteen years old not giving consent in cardio respiratory arrest coagulopathy active hemorrhage known allergy to local anesthetics pregnant and lactating woman unstable vital signs altered mental status patients who received anesthesia outside

Design outcomes

Primary

MeasureTime frame
Comparison of analgesic efficacy and adverse events of Suprascapular nerve block compared to intravenous fentanylTimepoint: Patients in both arms are followed up at baseline, 30 minutes, 1 hour, 2 hours, 4 hours and 6 hours post intervention

Secondary

MeasureTime frame
1.reduction in painful time 2.requirement of additional anesthesia 3.interrater agreement on performing nerve block procedureTimepoint: Patients in both arms are followed up at 30 min, 60 min, 120 min, 240 min and 360 min post intervention

Countries

India

Contacts

Public ContactDr Anmol Chanda

AIIMS New Delhi

sanjeevbhoi@gmail.com8527050391

Outcome results

None listed

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