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Postoperative Sleep Quality of Patients Anesthesia With Propofol or Sevoflurane Undergoing Thyroidectomy

NCT02146976 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 124

Last updated 2016-01-29

No results posted yet for this study

Summary

The investigators designed a study to determine whether Propofol or Sevoflurane would provide same postoperative sleep quality in patients undergoing thyroidectomy.

Conditions

  • Postoperative Sleep Quality

Interventions

DRUG

propofol

introvenious infusion of propofol

DRUG

sevoflurane

sevoflurane (1.0-1.3 Minimum Alveolar Concentration)

Sponsors & Collaborators

  • China Medical University, China

    lead OTHER

Principal Investigators

  • Hong Ma, M.D.,Ph.D. · the Anesthesiology Department

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2014-10-31
Primary Completion
2015-09-30
Completion
2015-10-31

Countries

  • China

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 NCT02146976 on ClinicalTrials.gov