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comparing intravenous lignocaine and fentanyl for endoscopic colon examination

Comparison of Intravenous Fentanyl and Lignocaine as adjuvant to Propofol based sedation for Colonoscopy- A Randomized Double Blind Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/08/015477
Enrollment
100
Registered
2018-08-27
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: K929- Disease of digestive system, unspecified

Interventions

Control Intervention1: fentanyl,lignocaine: use of fentanyl along with propofol for sedation in colonoscopy in comparison with lignocaine Control Intervention2: lignocaine: use of lignocaine along wit

Sponsors

blk superspeciality hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA I and II

Exclusion criteria

Exclusion criteria: 1) Refractory hemodynamic instability, including: a. SBP b. HR c. 2nd & 3rd degree AV block-. d. Patients with history of cardiac arrhythmias 2) Clinically significant liver/renal dysfunction. 3) Neurovascular patients with a history of CVA/TIA. 4) Pregnancy or breast feeding. 5) Patient with history of allergy to local anaesthetic drugs. 6) Procedure duration more than 30 minutes.

Design outcomes

Primary

MeasureTime frame
1. To compare the total consumption of propofol between lignocaine and fentanyl group during colonoscopy. 2. To compare time taken to recover from sedation after procedure. 3. To compare time taken to attain discharge fitness.Timepoint: at 0 minutes(prior to sedation), every 5 minutes after that till discharge criteria are met.

Secondary

MeasureTime frame
Colonoscopy Satisfaction Score Patient Pain ScoreTimepoint: 1 year

Countries

India

Contacts

Public Contactvarun aggrawal

Anesthesiology

drshriprakashsingh@blkhospital.com9810072232

Outcome results

None listed

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