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COMPARISON OF ATRACURIUM VERSUS CIS-ATRACURIUM REGARDING DURING GENERAL ANAESTHESIA

Compare Atracurium Versus Cis-atracurium on basis of Haemodynamic parameters, Time of Onset and Intubating Conditions during General anaesthesia - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/075659
Enrollment
86
Registered
2024-10-23
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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: Atracurium: Atracurium is an intermediate-acting, non-depolarizing neuromuscular blocking drug of benzylisoquinolinium class used for endotracheal intubation and provide skeletal muscle

Sponsors

Jawaharlal Nehru Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: This research study will include ASA Grades I and II patients between the ages of 18 and 60 who are scheduled for elective surgery and will require general anaesthesia with endotracheal intubation and do not have any concomitant diseases.

Exclusion criteria

Exclusion criteria: 1. Grades III and IV of the ASA 2. Mallampati Grade III and Mallampati Grade IV are both excluded. 3. Expected difficult airway 4. Comorbid systemic problems, including cardiovascular, hepatic, and renal dysfunction, as well as neuromuscular abnormalities. 5. Patients using aminoglycosides, MgSO4 6. Any known allergy to any of the study medications. 7. Women who are pregnant.

Design outcomes

Primary

MeasureTime frame
Atracurium is a more effective neuromuscular blocking agent than cisatracurium at the same dose, while higher doses of cisatracurium provide efficient, more rapid onset, with longer duration of action, stable hemodynamic status with no signs of histamine release clinically.Timepoint: At baseline, 0 minute, 1 minute, 3 minutes, 5 minutes.

Secondary

MeasureTime frame
The onset time, duration of action and haemodynamic parameters will be assessed.Timepoint: 1 minute, 3 minutes, 5 minutes after intubation.

Countries

India

Contacts

Public ContactDr Neeta Verma

Datta Meghe Institute of Medical Science and research

neetachaudhary1234@gmail.com9589715074

Outcome results

None listed

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