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To study the effect of intravenous lignocaine infusion on spinal anaesthesia in patients undergoing total knee replacement.

Effect of intravenous lignocaine infusion on subarachnoid anaesthesia in patients undergoing total knee replacement;A Randomised double blind controlled study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/12/038538
Enrollment
28
Registered
2021-12-09
Start date
Unknown
Completion date
Unknown
Last updated
2023-12-19

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: intravenous infusion of lignocaine: Effect of lignocaine infusion of 1.5mg/kg loading dose followed by intravenous infusion of 1.5 mg/kg/hr lignocaine prepared in a volume of 20ml/hr fo

Sponsors

Amulya Kodkani
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American College of Anaesthesiologists(ASA) physical status grade 1

Exclusion criteria

Exclusion criteria: 1.Revision Total Knee Replacement 2.Contraindications to spinal anaesthesia or previous failed spinal anaesthesia 3.Allergy to lidocaine 4.History of long standing diabetes mellitus,cardiac or neurological disease 5.Impaired Renal or Hepatic Function 6.Psychiatric illness affecting pain perception e.g severe depression,anxiety disorder 7.chronic Pain,other than chronic knee pain 8.Alcohol or substance abuse,regular use of strong opiods 9.Patients with obesity,anticipated difficult airway 10.Pregnant patients

Design outcomes

Primary

MeasureTime frame
Duration of sensory block after spinal anaesthesiaTimepoint: T1-time to loss of pinprick at T10 dermatome T2-Time to achieve highest level of sensory block T3-Time to recovery of sensory block

Secondary

MeasureTime frame
total requirement of analgesia in first 24 hours after surgeryTimepoint: in the first 24 hours postoperatively;anaesthesiologist rating the quality of anaesthesiaTimepoint: after completion of the surgery;bispectoral index (BIS)Timepoint: every 5 mins throughout the surgical procedure;duration of motor block after spinal anaesthesiaTimepoint: from administration of spinal drug to the return of bromage scale score to 0;INTRAOPERATIVE HEMODYNAMICS -HR,SBP,DBP and MAPTimepoint: every 5 mins throughout the surgical procedure;onset of motor blockTimepoint: from administration of spinal drug to modified bromage scale score of 3;onset of sensory blockTimepoint: from administration of spinal drug upto absence of pin prick at the T10 dermatome;postoperative VAS scoreTimepoint: at 4,8,12 and 24 hours postoperatively;surgeons rating of quality of operative conditionsTimepoint: after completion of the surgery;time for first postoperative analgesic requestTimepoint: postoperative period;total intraoperative sedation ( midazolam ) requiredTimepoint: to achieve a Ramsay Sedation Score of 3 during the surgical procedure

Countries

India

Contacts

Public ContactAnju R Bhalotra

Maulana Azad Medical College

drakgk@yahoo.co.in9968604219

Outcome results

None listed

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