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Effect of Dexmedetomidine Upon Sleep Postoperatively

NCT00333632 · Status: WITHDRAWN · Phase: PHASE4 · Type: INTERVENTIONAL

Last updated 2014-07-14

No results posted yet for this study

Summary

The purpose of this study is to determine whether an intravenous infusion of dexmedetomidine administered to surgical patients intra-operatively will improve the characteristics of sleep post-operatively.

Conditions

  • Sleep

Interventions

DRUG

Dexmedetomidine

DRUG

Propofol

DRUG

Midazolam

DRUG

Fentanyl

DRUG

Isoflurane

Sponsors & Collaborators

Principal Investigators

  • David B MacLeod, MD · Duke University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2006-06-30
Completion
2011-06-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Drugs
Companies

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 NCT00333632 on ClinicalTrials.gov