Comparison of face mask ventilation efficiency with early or late administration of muscle relaxant for better airway management: Double blinded randomised control study

Comparison of face mask ventilation efficiency before and after neuromuscular blockade: Double blinded randomised control study - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/05/067114

Enrollment

120

Registered

2024-05-09

Start date

Unknown

Completion date

Unknown

Last updated

2024-05-27

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: Giving NMBD before checking mask ventilation: After inducing the patient, the NMDB is also given as bolus of 0.1mg/kg for Vecuronium or 0.5mg/kg for Atracurium without checking status a

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients of either gender aged 18-65 years of ASA I and II posted for elective surgery under general anaesthesia.

Exclusion criteria

Exclusion criteria: Anticipated difficult airway Patient refusal Allergy to the study drug

Design outcomes

Primary

Measure	Time frame
Vte at 30, 60, 90, 120, 150 and 180s for a total of 180s of face mask ventilation after cessation of response using mechanical ventilator.Timepoint: At 30, 60, 90, 120, 150 and 180 seconds	—

Secondary

Measure	Time frame
Ease of laryngoscopy (vocal cord movement, limb movement, and coughing)Timepoint: Throughtout intubation;Han’s grading for face mask ventilationTimepoint: During apneic ventilation;Intubation timeTimepoint: From laryngoscopy to appreance of first capnography wave	—

Countries

India

Contacts

Public ContactDr Varun Kumar S

Sri Ramachandra Medical College and Research Hospital

vjram2001@yahoo.co.in9841219820

Outcome results

None listed

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