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A study to find minimum volume of a particular local painkiller drug required for ultrasound guided forearm nerve block

A study to find minimum effective volume of 0.5% ropivacaine for ultrasound guided costoclavicular block

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/01/022714
Enrollment
50
Registered
2020-01-13
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- A patient with elbow , wrist or hand injury Health Condition 2: S529- Unspecified fracture of forearm Health Condition 3: S529- Unspecified fracture of forearm

Interventions

Intervention1: volume for costoclavicular block: In ultrasound guided costoclavicular block with 0.5 % ropivacaine , first candidate will receive 20ml of drug depending upon the success or failure of

Sponsors

all india institute of medical sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All adults posted for surgeries of elbow , forearm , wrist and hand American society of anaesthesia grade I/II patient Body mass index 18 to 30 kg/ m sq

Exclusion criteria

Exclusion criteria: Patients refusal for brachial plexus block Sepsis coagulopathy Known neuropathy or injury of musculocutaneous , radial , ulnar or median nerve Known allergy to local anaesthetic drugs Abnormal neck or shoulder anatomy Previous surgery in infraclavicular fossa

Design outcomes

Primary

MeasureTime frame
to calculate mev of ropivacaine in 90% of patients for costocavicular bliockTimepoint: Adequate surgical anaesthesia at 30 minutes post block assessment interval

Secondary

MeasureTime frame
1.Supplementation required to achieve adequate surgical anaesthesia 2.Tourniquet pain 3.Onset time of adequate surgical anaesthesia 4.Block performance time 5.Incidence of immediate complications like vascular puncture, pleural puncture, paresthesias or local anaesthetic toxicity. Delayed complications like persistent paresthesias and motor deficit will be enquired one week after the block Timepoint: nil

Countries

India

Contacts

Public Contactchhavi sawhney

All India Institute of Medical Sciences, new delhi

drchhavisawhney@gmail.com9818357051

Outcome results

None listed

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