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Pupillary Diameter Under Different Concentrations of Propofol

NCT02998424 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2018-06-26

No results posted yet for this study

Summary

Resting pupillary diameter was measured at a randomized Effect-site target concentration of propofol used as a sole anesthetic.

Conditions

  • Anesthesia

Interventions

DRUG

Propofol

Continuous infusion

DEVICE

Pupillary diameter measurement

Instantaneous measure

Sponsors & Collaborators

  • Hôpital Armand Trousseau

    lead OTHER

Principal Investigators

  • Isabelle Constant, MD-PHD · Hopital Armand Trousseau, Université Paris 6, Département d'anesthésie

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
13 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-05-31
Primary Completion
2016-10-31
Completion
2016-12-31

Countries

  • France

Study Locations

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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 NCT02998424 on ClinicalTrials.gov