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A study comparing two different methods for evaluation of brachial plexus block

Correlation between two monitoring tool by subjective and objective method for evaluation of adequacy of brachial plexus block:an observational study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2020/01/023066
Enrollment
100
Registered
2020-01-31
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: S599- Unspecified injury of elbow and forearm

Interventions

Intervention1: Nil: Nil Control Intervention1: Nil: Nil

Sponsors

Department of Anesthesiology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All the male and female patients of age between 20 to 60 with upper limb fractures of ASA grade I and II with written informed consent

Exclusion criteria

Exclusion criteria: Refusing consent, diabetic, drug allergy, bleeding disorder, systemic illness, psychiatric illness, previous nerve injury, on anticoagulants, antenatal female, history of drug dependence

Design outcomes

Primary

MeasureTime frame
Time for peak effect of motor block by perfusion index and pin prickTimepoint: 30 min—

Secondary

MeasureTime frame
Vital Parameters, Surgeons satisfaction, supplementation to brachial block needed or notTimepoint: 30minutes—

Countries

India

Contacts

Public ContactDr Komal Shah

goverment medical college bhavnagar

shah.komal@rediffmail.com9427215252

Outcome results

None listed

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