Prospective Randomized Controlled Study Comparing injection Lignocaine Infusion Versus injection Magnesium Infusion for surgery Outcomes in Optimized Reactive Airway Disease Patients for Laparoscopic Surgeries

Prospective Randomized Control Study Comparison of IV Lignocaine Infusion Versus Magnesium Infusion for Perioperative Outcomes in Optimized Reactive Airway Disease Patients for Laparoscopic Surgeries - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/05/087130

Enrollment

Registered

2025-05-20

Start date

Unknown

Completion date

Unknown

Last updated

2025-05-26

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

Conditions

Health Condition 1: J958- Other intraoperative and postprocedural complications and disorders of respiratory system, not elsewhere classified

Interventions

Intervention1: magnesium sulphate and lidocaine: For Group A After Routine induction Lignocaine 1.5 mg/kg i.v. bolus diluted to 10 mL with normal saline given and 1.5 mg/kg/hour i.v. infusion was cont

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age 18-60, both male and female patient 2.reactive airway Patient undergoing elective laparoscopic surgery 3.American Society of Anesthesiologists (ASA) physical status I -II.

Exclusion criteria

Exclusion criteria: 1.Contraindications to iv lignocaine and mgso4. 2.Refusal to participate. 3.Severe cognitive impairement. 4.Previous participations for same study. 5.Significant comorbities uncontrolled DM, CVD, & CKD etc.

Design outcomes

Primary

Measure	Time frame
Perioperative OutcomeTimepoint: 2hour, 4hour,6hour,8hour,12hour,24hour	—

Secondary

Measure	Time frame
Secondary objectives 1.Hospital stay 2.SafetyTimepoint: 2 hour, 4 hour,6 hour,8 hour,10 hour,12 hour, 24 hour	—

Countries

India

Contacts

Public ContactDr Swati Verma

GSVM Medical College

chandrashekhar77@gmail.com9236072730

Outcome results

None listed

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