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EFFECT OF 2% LIGNOCAINE INJECTION ON PROPOFOL CONSUMPTION IN PATIENTS UNDERGOING COLONOSCOPY

Not yet recruiting
Conditions
Diseases of the digestive system,
Registration Number
CTRI/2023/03/050700
Lead Sponsor
Dr Freeda Praveena Cutinha
Brief Summary

- This study aims at evaluating whether Intravenous 2% Lignocaine Hydrochloride administration can reduce Propofol dose requirement, and pain reduction on injection of propofol.

- To study the effect of 2% Intravenous Lignocaine Hydrochloride with Propofol in preserving hemodynamic and respiratory normality.

- To compare the ease ofprocedure for endoscopists and patient satisfaction and comfort during theprocedure

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
70
Inclusion Criteria
  • Adults aged more than 20 years and less than 60 years.
  • Patients with American Society of Anaesthesiolgists(ASA I and II).
  • Patients scheduled for colonoscopy.
  • Time for the procedure fewer than 45 mins.
Exclusion Criteria
  • Age less than 20 years and more than 60 years.
  • American society of Anaesthesiologists(ASA) III and above.
  • Procedure time more than 45 minutes.
  • Pregnancy and Lactation.
  • Pre-existing hypoxemia( Pulse oximetry SpO2<90%) Hypotension (Systolic blood pressure <90mmHg) Bradycardia(Heart rate<50beats/minute) Uncontrolled Hypertension(Systolic blood pressure >170mmHg, Diastolic blood pressure >100 mmHg) Respiratory Insufficiency.
  • Severe Renal or Liver Failure.
  • Allergy to Lignocaine.
  • Atrioventricular block.
  • Neuropsychiatric disorders using sedative hypnotics.
  • Analgesics >3 months .
  • Previous colectomy.
  • Hyperalgesia or Refractory cancer pain.
  • Intravenous anesthesia contraindication.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Recovery time.During induction | After induction | 1 min | 3 mins | 5 mins | 10 mins | 15 mins | 20 mins | 25 mins | 30 mins | 35 mins | 40 mins | 45 mins | At the end of procedure | At the time of recovery | 1 hour | 2 hour
Induction Dose of Propofol for the Procedure.During induction | After induction | 1 min | 3 mins | 5 mins | 10 mins | 15 mins | 20 mins | 25 mins | 30 mins | 35 mins | 40 mins | 45 mins | At the end of procedure | At the time of recovery | 1 hour | 2 hour
Maintenance Dose of Propofol for the Procedure.During induction | After induction | 1 min | 3 mins | 5 mins | 10 mins | 15 mins | 20 mins | 25 mins | 30 mins | 35 mins | 40 mins | 45 mins | At the end of procedure | At the time of recovery | 1 hour | 2 hour
Total amount of Propofol administered during the procedure.During induction | After induction | 1 min | 3 mins | 5 mins | 10 mins | 15 mins | 20 mins | 25 mins | 30 mins | 35 mins | 40 mins | 45 mins | At the end of procedure | At the time of recovery | 1 hour | 2 hour
Induction time.During induction | After induction | 1 min | 3 mins | 5 mins | 10 mins | 15 mins | 20 mins | 25 mins | 30 mins | 35 mins | 40 mins | 45 mins | At the end of procedure | At the time of recovery | 1 hour | 2 hour
Secondary Outcome Measures
NameTimeMethod
1. Intra Operative Hemodynamic Variables.-Heart Rate (HR).

Trial Locations

Locations (1)

Kasturba Medical College Hospitals.

🇮🇳

Kannada, KARNATAKA, India

Kasturba Medical College Hospitals.
🇮🇳Kannada, KARNATAKA, India
Dr Freeda Praveena Cutinha
Principal investigator
8197967512
freeda810@gmail.com

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