Comparaing Intubating Conditions After Administration Of Rocuronium And Succinylcholine For Endotracheal Intubation In Paediatric Patients

Comparative Study Of Intubating Conditions After Administration Of Rocuronium And Succinylcholine For Endotracheal Intubation In Paediatric Patients - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/03/105901

Enrollment

106

Registered

2026-03-11

Start date

Unknown

Completion date

Unknown

Last updated

2026-03-30

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: Succinylcholine: Intubating Conditions after administration of 2mg/kg Succinylcholine during induction for endotracheal intubation in paediatric patients Control Intervention1: Rocuroni

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade I or II fit patients Paediatric patients aged between 5 and 12 years of age Patients undergoing paediatric surgeries under GA Hemodynamically stable patients with all routine investigations within normal limits without any comorbidities. Written informed consent from concerned parents

Exclusion criteria

Exclusion criteria: Patients who are not willing to participate in the study Patients with ASA grade III and above physical status Patients who are aged less than 5 or more than 12 Patients posted for emergency procedures Patients with known allergy to study drugs Patients with known neuromuscular disease History of cardiac/renal/hepatic disorders Patient receiving medications known to influence neuromuscular function Patients with difficult intubation Patients suffering from acute respiratory illness

Design outcomes

Primary

Measure	Time frame
To compare onset of action, assess intubating conditions after administration of succinylcholine and rocuronium and time required to optimum intubating conditionsTimepoint: Intubating conditions will be assessed at 60 seconds according to the four-point scale of Cooper et al. Tracheal intubation will not be performed until the intubating conditions are excellent or good according to the scale. Subsequent intubation attempts will be assessed if required and noted accordingly	—

Measure

Time frame

To compare onset of action, assess intubating conditions after administration of succinylcholine and rocuronium and time required to optimum intubating conditionsTimepoint: Intubating conditions will be assessed at 60 seconds according to the four-point scale of Cooper et al. Tracheal intubation will not be performed until the intubating conditions are excellent or good according to the scale. Subsequent intubation attempts will be assessed if required and noted accordingly

—

Secondary

Measure	Time frame
To compare onset of action, assess intubating conditions after administration of succinylcholine and rocuronium and time required to optimum intubating conditionsTimepoint: Haemodynamic monitoring after Injecting the drug, During laryngoscopy, Post intubation - 1 min, 5min and 10 min, End of surgery and Post extubation and observe side effects if any	—

Countries

India

Contacts

Public ContactDr Chhaya Suryawanshi

Dr. D. Y. Patil Medical College, Hospital and Research Centre

chhayasuryawanshi@gmail.com9922888201

Outcome results

None listed

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