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Evaluation of propofol sparing effect of intravenous lignocaine in patients undergoing daycare upper Gastro Intestinal endoscopic procedures

Evaluation of propofol sparing effect of intravenous lignocaine in patients undergoing daycare upper G.I. endoscopic procedures

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/10/028697
Enrollment
90
Registered
2020-10-28
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: - Health Condition 2: K87- Disorders of gallbladder, biliarytract and pancreas in diseases classified elsewhere Health Condition 3: O- Medical and Surgical Health Condition 4: K831- Obstruction of bile duct

Interventions

Intervention1: Lignocaine: Patients will receive perioperative intravenous bolus of 1.5â??mg/kg lignocaine over 10â??seconds (2% lignocaine) followed by 4â??mg/â??kg/â??hour continuous lidocaine infus

Sponsors

Indira Gandhi Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of age 18-65 years ASA Grade-I & II Undergoing day care upper G.I. endoscopic procedures under sedation

Exclusion criteria

Exclusion criteria: Patient refusal ASA Grade-III & IV Unstable hemodynamic status Mental disorders, such as schizophrenia and psychosis on long-term psychotropic drugs Hyperalgesia or refractory cancer pain Allergic to study agent

Design outcomes

Primary

MeasureTime frame
1. Total amount of propofol administered during the procedure 2. Total supplemental amount of propofol after induction and 3. Number of boluses of supplemental propofol Timepoint: After procedure

Secondary

MeasureTime frame
Recovery scores VAS scoreTimepoint: postoperatively

Countries

India

Contacts

Public ContactMumtaz Hussain

Indira Gandhi Institute of Medical Sciences

drhussain72@yahoo.co.in9973152076

Outcome results

None listed

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