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

Effect of Preservative free 2% Lignocaine Hydrochloride on Propofol consumption in patients undergoing colonoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/03/050700
Enrollment
70
Registered
2023-03-15
Start date
Unknown
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Health Condition 1: K00-K95- Diseases of the digestive system

Interventions

None listed

Sponsors

Dr Freeda Praveena Cutinha
Lead Sponsor

Eligibility

Inclusion criteria

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. BMI Time for the procedure fewer than 45 mins.

Exclusion criteria

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 Hypotension (Systolic blood pressure Bradycardia(Heart rate 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. Epilepsy.

Design outcomes

Primary

MeasureTime frame
Induction Dose of Propofol for the Procedure. Maintenance Dose of Propofol for the Procedure. Total amount of Propofol administered during the procedure. Induction time. Recovery time.Timepoint: 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

MeasureTime frame
1. Intra Operative Hemodynamic Variables. -Heart Rate (HR). -Systolic Blood Pressure (SBP). -Diastolic Blood Pressure (DBP). -Mean Arterial Pressure (MAP). -Oxygen Saturation (SpO2). -Respiratory Rate (RR). 2.Pain Reduction on Injection with Propofol assessed by VAS 1-10. 3.Ease of Procedure for Endoscopist assessed 6-point Likert Scale. 4.Recovery time. 5.Patient Satisfaction and comfort during the procedure assessed by 6-point Likert scale and Modified Gloucester comfort scale respectively. 6.Post Procedure events -Pain and Fatigue assessed by VAS 1-10. -Recall. -Dizziness. -Nausea and Vomiting. Timepoint: 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

Countries

India

Contacts

Public ContactDr Shaila S Kamath

Kasturba Medical College, Mangalore

shaila.kamath@manipal.edu9844090231

Outcome results

None listed

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