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Evaluation of effects of lignocaine infusion on postoperative pain relief for abdominal surgery.

Evaluation of effects of intravenous lignocaine infusion on postoperative analgesia after upper abdominal surgery.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/04/024743
Enrollment
30
Registered
2020-04-20
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: K87- Disorders of gallbladder, biliarytract and pancreas in diseases classified elsewhere Health Condition 2: K566- Other and unspecified intestinal obstruction

Interventions

Intervention1: Group Lignocaine ( Group L): Patients allotted to lignocaine (group L) will receive bolus dose of lignocaine 1.5 mg/kg through a dedicated intravenous line followed by an infusion@ 1.5m

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patients in age groups 18- 70 Healthy patients belonging to ASA PS I and II Patients undergoing elective upper abdominal surgery.

Exclusion criteria

Exclusion criteria: Inability to understand preoperative instructions regarding use of PCA pump or pain score Planned elective postoperative mechanical ventilation Patients known to be on anti-arrhythmic drug therapy History of COPD, cardiac, hepatic, renal or nervous system disorder Known allergy to lignocaine

Design outcomes

Primary

MeasureTime frame
TIME INTERVAL between skin closure and first morphine PCA request. TOTAL MORPHINE CONSUMPTION at the end of 2nd, 6th, 12th, 24th and 36th postoperative hour. Timepoint: Immediate postoperative period 36 hours after surgery

Secondary

MeasureTime frame
PAIN SCORE (NRS) at rest, on deep inspiration, cough and movement (side to side or leg raising) at the end of 2nd, 6th, 12th, 24th and 36th postoperative hour. Any complaints of â??perioral numbness, light headedness. Sedation level Timepoint: Immediate postoperative period 36 hours after surgery

Countries

India

Contacts

Public ContactDr Lokvendra Singh Budania

Kasturba Medical College, Manipal, Manipal Academy Of Higher Education

eeshwar.kmc@gmail.com9740122272

Outcome results

None listed

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