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A study on infraclavicular block ultrasound for upper limb surgeries

A Randomised controlled trial to compare the efficacy of single versus triple injection technique for ultrasound-guided infraclavicular block in upper limb surgeries

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/06/043301
Enrollment
50
Registered
2022-06-16
Start date
Unknown
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

Health Condition 1: S520- Fracture of upper end of ulna

Interventions

Intervention1: NIL: NIL Intervention2: ultrasound-guided infraclavicular block of triple injection technique: A 7 to 13 MHz linear probe will be placed in the deltopectoral groove in the sagittal plan

Sponsors

SRM Medical College Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged from 18-65 years of both sexes ASA grade I-III BMI

Exclusion criteria

Exclusion criteria: Not willing to participate Coagulopathy Sepsis Hepatic or Renal Failure Pregnancy Allergy to Local anaesthetics Pre-existing Musculocutaneous/Median/ Radial/Ulnar Neuropathy Prior Surgery in The Infraclavicular Fossa

Design outcomes

Primary

MeasureTime frame
To compare the time of onsetof sensory and motor blockTimepoint: 18 MONTHS—

Secondary

MeasureTime frame
To compare the: 1.Time to perform the block. 2. duration of analgesia. 3. incidence of sparing- requiringsupplemental nerve blocks or conversion to GA. 4. Complications of block (Vascular puncture, Pneumothorax,Paresthesia, LA toxicity). 5. Intraoperative fentanyl consumption. 6.Post-operative analgesic consumption Timepoint: 18 MONTHS—

Countries

India

Contacts

Public ContactVEDAVYAS RAKSHA

SRM MEDICAL COLLEGE HOSPITAL AND RESEARCH CENTRE, CHENNAI

drcrsaravanan@gmail.com9884001153

Outcome results

None listed

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