MedTrace Logo

Adequacy of Anaesthesia for Colonoscopic Procedures

NCT03922815 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 158

Last updated 2020-10-23

No results posted yet for this study

Summary

The aim of this randomized prospective trial is to assess the utility of Adequacy of Anaesthesia technique (Response Entropy and Surgical Pleth Index) for monitoring pain perception intraoperatively and its influence on postoperative pain perception, both patients' and operators' satisfaction in patients undergoing colonoscopic procedures under intravenous sedation using propofol and fentanyl.

Conditions

  • Colonic Diseases, Functional

Interventions

DRUG

rescue fentanyl

a rescue dose of fentanyl 0,5 mcg per kilogram of body

DRUG

rescue propofol

propofol in a single dose of 0,5 mg/kg of body weight

Sponsors & Collaborators

  • Medical University of Silesia

    lead OTHER

Principal Investigators

  • Michał J Stasiowski, M.D · Medical University of Silesia

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-09-01
Primary Completion
2020-01-31
Completion
2020-01-31

Countries

  • Poland

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03922815 on ClinicalTrials.gov