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Desflurane and Postoperative Sleep Quality in Patients Undergoing Elective Breast Surgery | Clinical Trials | Clareo Health

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Desflurane and Postoperative Sleep Quality in Patients Undergoing Elective Breast Surgery

Effect of Desflurane on Postoperative Sleep Quality in Patients Undergoing Elective Breast Surgery: A Non-inferiority Randomized Controlled Trial

NCT04805775•Zhongnan Hospital

View on ClinicalTrials.gov

Summary

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

Eligibility

Age

18 - 75 years

Sex

FEMALE

Healthy Volunteers

Yes

Inclusion Criteria

•1. Undergoing elective breast surgery
•2. Age 18-75 years old
•3. ASA-PS grade I or II
•4. Those who voluntarily participate in the research and sign the informed consent

Exclusion Criteria

•1. Cognitive impairment (MMSE \<27) before the operation
•2. The patients received adjuvant chemotherapy before the operation
•3. At present, they are taking psychoactive, opioid, anti-anxiety, and hypnotic drugs
•4. Known or treated patients with obstructive sleep apnea
•5. Patients with other cancers

Locations (1)

Zhongnan Hospital of Wuhan University

Wuhan, Hubei, China

Key Dates

Start Date

October 21, 2021

Primary Completion Date

September 9, 2022

Completion Date

March 10, 2023

Last Updated

May 31, 2023

Enrollment

118

ACTUAL participants

Conditions

DesfluranePropofolPostoperative SleepPSQIBreast Tumor

Interventions

Desflurane Inhalation

DRUG

Induction Agent Choice With Early Mortality and Prognostic Outcomes in Critically Ill Patients

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RECRUITING

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: May 31, 2023Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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Desflurane and Postoperative Sleep Quality in Patients Undergoing Elective Breast Surgery

Inclusion Criteria

Exclusion Criteria

Induction Agent Choice With Early Mortality and Prognostic Outcomes in Critically Ill Patients

Minto and Eleveld Remifentanil Target Controlled Infusion (TCI) Models: a Clinical Comparison

A Comparative Study of Eleveld and Schnider Pharmacokinetic Models for Target-Controlled Infusion of Propofol in Sedation of Mechanically Ventilated ICU Patients

Hemodynamic Effects of a High Dose Versus Low Dose Propofol During Induction of Anesthesia.

The Effect of Dexmedetomidine and Esketamine Combined Infusion Quality of Sleep Undergoing Modified Radical Mastectomy

Propofol-Fentanyl-Dexmedetomidine and Propofol-Fentanyl-Sevoflurane Anesthesia for Major Spine Surgery Under Somato Sensory- and Motor- Evoked Potential Monitoring