A study to compare the efficacy of sevoflurane versus propofol in patients undergoing brachial plexus repair surgery

A comparative randomized control study of induction and maintenance of general anaesthesia with sevoflurane versus propofol without neuromuscular blockers for brachial plexus repair surgery

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2021/12/038639

Enrollment

Registered

2021-12-15

Start date

Unknown

Completion date

Unknown

Last updated

2022-02-21

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

Conditions

Health Condition 1: S143- Injury of brachial plexus

Interventions

Intervention1: Sevoflurane: Inhalational induction with 8% Sevoflurane and maintenance with 3% sevoflurane throughout the procedure Control Intervention1: Propofol: Intravenous induction with 3mg/kg

Eligibility

Inclusion criteria

Inclusion criteria: 1) Adults of age between 18 to 45 years, 2) ASA grade I and II,3)Mallampatti grade 1 and 2, 4)Informed consent from the patient, 5)Patient diagnosed with brachial plexus injury undergoing brachial plexus repair surgery

Exclusion criteria

Exclusion criteria: 1)patient not giving consent, 2)patient having coexisting cardiovascular,renal,respiratory,endocrinal and metabolic disorders 3)patient whose physical characteristics suggest difficult intubation (MP III and IV) 4)Non brachial plexus repair surgeries

Design outcomes

Primary

Measure	Time frame
Ease of intubation in both the groups Hemodynamic stability in both groupsTimepoint: Baseline,1minute, 5 minutes, 10 minutes, 20 minutes, 1 hour, 2 hour and 3 hours	—

Secondary

Measure	Time frame
Emergence timeTimepoint: After surgical procedure	—

Countries

India

Contacts

Public ContactDr Mhonisha B

Ganga Medical Centre and Hospitals

drboopathiv@yahoo.co.in9443338677

Outcome results

None listed

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