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To compare the effects of cisatracurium and atracurium on levels of tryptase, Ig E and absolute eosinophil count in adult patients undergoing general anesthesia for elective surgery.

Comparison of effects of cisatracurium and atracurium upon Tryptase, IgE levels and Absolute eosinophil counts in adult patients undergoing general anesthesia for elective surgery.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/09/036550
Enrollment
80
Registered
2021-09-15
Start date
Unknown
Completion date
Unknown
Last updated
2023-10-16

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 Health Condition 2: 8- Other Procedures

Interventions

Control Intervention1: Inj Atracurium Besylate: Blood samples will be taken from patients at following times: i. before induction, ii.one and two hours after giving first dose of study drug (Inj Atrac

Sponsors

ABVlMS and Dr RML hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Consenting adult patients with ASA Grade 1/2 and modified Mallampati grade 1/2

Exclusion criteria

Exclusion criteria: Patients with anticipated difficult airway. Patients with peripheral neuropathy, diabetes mellitus, neuromuscular disorders and myopathies. Patients on antibiotics (e.g., aminoglycosides, tetracyclins, bacitracin, lincomycin, clindamycin, colistin). Patients on drugs like Magnesium sulphate, lithium, procainamide and quinidine. Patients with history of atopy and asthma. Patients with known allergy to any of the drugs involved in study. pregnant patients.

Design outcomes

Primary

MeasureTime frame
Patients tryptase levels,IgE levels, absolute eosinophil count, hemodynamic parameters (heart rate and SBP/DBP), cilinical side effects ( flushing of skin, rashes, hypotension, tachycardia, bronchospasm, anaphylaxis, arrhythmias)Timepoint: Blood samples will be taken before induction , one and two hour after giving first dose of study drug and additional sample if and when any side effects occurs.

Secondary

MeasureTime frame
nilTimepoint: nil

Countries

India

Contacts

Public ContactDr Vijay Kumar Nagpal

ABVIMS and Dr RMLH, New Delhi

nagpalvijaykumar@gmail.com09968304240

Outcome results

None listed

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