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Atracurium dose efficacy & timing comparision in rapid sequence intubation

DETERMINATION OF DOSE AND EFFICACY OF ATRACURIUM FOR RAPID SEQUENCE INDUCTION OF ANAESTHESIA: A RANDOMIZED PROSPECTIVE STUDY"

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/08/044610
Enrollment
100
Registered
2022-08-03
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: J439- Emphysema, unspecified Health Condition 2: O666- Obstructed labor due to other multiple fetuses Health Condition 3: K652- Spontaneous bacterial peritonitis

Interventions

Control Intervention1: Atracurium: 0.75mg/kg IV loading dose only for intubation Control Intervention2: Atracurium: DOSE OF 0.75MG/KG IV loading dose for intubation Control Intervention3: ATRACURIUM:

Sponsors

Manchala priyanka
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age group of 20 to 65 years of ASA grades I and II of both sexes

Exclusion criteria

Exclusion criteria: Patients of ASA grades III and IV. Age less than 20 years and greater than 65 years

Design outcomes

Primary

MeasureTime frame
Time taken for intubation in 0.75mg/kg/mim vs 1mg/kg/min doses comparisionTimepoint: time taken for intubation 60sec 90sec 120sec—

Secondary

MeasureTime frame
ease of intubation and cardiovascular haemodynamics in 0.75mg/kg/mim and 1mg/kg/minTimepoint: preinduction 1min 3min 5min pre intubation 1min 3min 5min post intubation 1min 3min 5min—

Countries

India

Contacts

Public ContactMANCHALA PRIYANKA

BLDE deemed to be university

drvijay8@gmail.com9844095250

Outcome results

None listed

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