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The Quality of Recovery After General Anesthesia With Desflurane and Sevoflurane in Endoscopic Ureteral Lithotripsy

The Quality of Recovery After General Anesthesia With Desflurane and Sevoflurane in Endoscopic Ureteral Lithotripsy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04712162
Enrollment
60
Registered
2021-01-15
Start date
2019-11-19
Completion date
2020-05-07
Last updated
2021-01-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia

Brief summary

The good quality of recovery after general anesthesia is one of goals for short procedures and ambulatory surgeries. The study's objective was to compare the quality of recovery after general anesthesia with desflurane and sevoflurane with laryngeal mask airway for endoscopic ureteral lithotripsy.

Detailed description

This is a randomized controlled trial. There were 60 cases of endoscopic ureteral lithotripsy under general anesthesia with laryngeal mask airway were enrolled. All cases were randomly divided into two group (desflurane or sevoflurane). Each group had 30 cases. Primary outcome was time to awakening. Secondary outcomes were time to wash-out of volatile anesthetics, time to extubation, irritation after awakening, and modified Aldrete score. Statistical analysis was performed by using Kaplan-Meieir curve and log-rank test for time to adequate depth of anesthesia and time to awakening; t-test for time to wash-out of volatile anesthetics; chi-square test for depth of anesthesia by PRST score, irritation after awakening and Aldrete score; Fisher test for adverse effects of volatile anesthetics. The research was approved by Gia Dinh People Hospital ethics committee

Interventions

OTHEROther

Compare time to awakening and quality of recovery after general anesthesia between two groups.

Sponsors

Gia Dinh People Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* All eligible subjects who underwent endoscopic ureteral lithotripsy under general anesthesia * ASA I and II

Exclusion criteria

* Contraindication to laryngeal mask airway. * Indication for conversion to tracheal intubation during surgery. * History of malignant hyperthermia. * Pregnancy. * Obese (BMI \>25 kg/m2). * Substances abuse.

Design outcomes

Primary

MeasureTime frameDescription
Time to awakeningAfter stopping volatile anesthetics to patient awakening, up to 30 minutes.Time required for awakening

Secondary

MeasureTime frameDescription
Time to wash-out of volatile anestheticsAfter stopping volatile anesthetics to complete wash-out of volatile anesthetics, up to 30 minutesTime required for washing out volatile anesthetics
Time to extubationAfter stopping volatile anesthetics to readiness for extubation, up to 30 minutesTime required for successful extubation.
Irritation after awakeningAfter awakening to eligible discharge, up to 2 hours.Aono score \>2
Adverse effects of volatile anestheticsAfter providing volatile anesthetics until they were stopped, up to 90 minutesHypotension, cough, nausea and vomitting.

Countries

Vietnam

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026