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Ultrasound guided Costoclavicular versus Supraclavicular Block in Upper Limb Orthopaedic Surgeries

A Comparative study of Ultrasound guided Costoclavicular versus Supraclavicular Block in patients undergoing Upper Limb Orthopaedic Surgeries. - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112629
Enrollment
100
Registered
2026-06-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: S525- Fracture of lower end of radius Health Condition 2: S526- Fracture of lower end of ulna Health Condition 3: S523- Fracture of shaft of radius Health Condition 4: S522- Fracture of shaft of ulna Health Condition 5: S521- Fracture of upper end of radius Health Condition 6: S520- Fracture of upper end of ulna

Interventions

Intervention1: Costoclavicular Block: Ultrasound Guided Costoclavicular Block with with 20ml of 18 ml Inj Ropivacaine 0.75% + 2ml Dexamethasone(8mg) given intra operatively Control Intervention1: Supr

Sponsors

Gujarat Cancer Society Medical College Hospital and Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients who are willing with informed consent 2. Age 18-70 years 3. Either Gender 4. ASA grade1/2/3

Exclusion criteria

Exclusion criteria: 1. Unwilling to participate/Refusing to consent 2. Contraindication to regional anesthesia 3. Pregnant Women 4. Infection at site of needle insertion 5. Coagulopathies 6. Contralateral phrenic nerve paralysis 7. Hypersensitivity to study drug 8. Significant pulmonary pathology 9. Bilateral forearm surgeries. 10. Major systemic illnesses 11. ASA 4/5

Design outcomes

Primary

MeasureTime frame
Primary Objectives: Block Performance Time Time of Onset of Sensory and Motor Block Time to achieve complete sensory and motor block Timepoint: 0 min 5 min 15 min 20 min until effect of block occurs

Secondary

MeasureTime frame
Total duration of analgesia by NRS Score Time to first rescue analgesia Total dose of post-operative analgesia received in first 24hr period Complications (if any)Timepoint: 0 min 5 min 15 min 20 min 30 min 60 min 90 min 120 min or until block effect wears off & NRS score more than 5

Countries

India

Contacts

Public ContactDr. Divya Kheskani

Gujarat Cancer Society Medical College Hospital and Research Centre

divya.kheskani@gmail.com8980738209

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026