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Desflurane and Postoperative Sleep Quality in Patients Undergoing Elective Breast Surgery

NCT04805775 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 118

Last updated 2023-05-31

No results posted yet for this study

Summary

This study intends to investigate the effects of desflurane on postoperative sleep quality to guide perioperative patient management.

Conditions

  • Desflurane
  • Propofol
  • Postoperative Sleep
  • PSQI
  • Breast Tumor

Interventions

DRUG

Desflurane Inhalation

Subjects were randomized in a 1:1 ratio to undergo breast surgery under maintenance of anesthesia with the classical intravenous anesthetic drug propofol (reference group) or the inhaled anesthetic drug desflurane (test group).

Sponsors & Collaborators

  • Zhongnan Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-10-21
Primary Completion
2022-09-09
Completion
2023-03-10

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 NCT04805775 on ClinicalTrials.gov