Skip to content

Comparative study of ultrasound guided infraclavicular block versus retroclavicular block with 0.5 percent levobupivacaine

Comparison between Ultrasound guided infraclavicular block versus retroclavicular block with 0.5 percent levobupivacaine - Nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088054
Enrollment
76
Registered
2025-06-02
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Interventions

Intervention1: Infraclavicular block, retroclavicular block: Ultrasound guided infraclavicular block versus retroclavicular block using 0.5% levobupivacaine in orthopedic surgery of upper limb Control

Sponsors

Department of Anaesthesia and critical care and pain medicine
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients willing to participate in study. Patients above the age of 18 years having the concerned disease. Elective surgery of the hand, wrist, forearm or elbow. Able to provide valid written consent.

Exclusion criteria

Exclusion criteria: Patients refusal Systemic or local infection at the needle entry point Coagulopathy Severe pulmonary condition Local anaesthetic allergy Pregnancy Preexisting neurologic symptoms in the ipsilateral limb

Design outcomes

Primary

MeasureTime frame
Extent and duration of motor and sensory block. Intraoperative and postoperative pain, assessment using VAS SCORE. Extent of block and duration of block assessed using dermatomal distribution at 30 min, 2 hours, 4 hours, 6 hours, 12 hours, 24 hours postoperatively.Timepoint: 5 min,10 min, 15 min, 20 min, 25 min,30 min, 2 hours, 4 hours, 6 hours, 12 hours, 24 hours

Secondary

MeasureTime frame
Needle visibility Block success rate Number of attempts to achieved full effect. Block performance time Procedure related pain, complications and patients and surgeon satisfaction.Timepoint: 5 min,10 min, 15 min, 20 min, 25 min,30 min, 2 hours, 4 hours, 6 hours, 12 hours, 24 hours

Countries

India

Contacts

Public ContactDr Chandrashekhar Singh

GSVM Medical College kanpur

chandrashekhar77@gmail.com9759101491

Outcome results

None listed

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