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NCT06423313 Clinical Trial

Effects of Anesthesia Type on QoR-40

General Anesthesia Clinical Trial

Official title:
The Comparison of Total Intravenous Anesthesia and Inhalation Anesthesia Effects on Postoperative Recovery by Quality of Recovery (QoR-40) in Septorhinoplasty

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT06423313
Other study ID # 2024/07-1
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date May 1, 2024
Est. completion date October 1, 2024

Study information
Verified date May 2024
Source Zonguldak Bulent Ecevit University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

To compare the effects of total intravenous anesthesia and inhalation anesthesia used for maintenance on postoperative recovery in patients undergoing septorhinoplasty surgery under general anesthesia, using the recovery quality score (QoR-40).

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 1
Est. completion date October 1, 2024
Est. primary completion date August 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - 18-65 years old - ASA I-II-III risk group - Patients whose consent was obtained with an informed consent form - Patients who will undergo septorhinoplasty surgery Exclusion Criteria: - -ASA >3 - Psychiatric illness that prevents them from answering the questionnaire - Patients with a history of chronic opioid and benzodiazepine use as it may affect recovery time - Severe renal and hepatic insufficiency - Severe respiratory and cardiovascular disease - Patients with a body mass index >30 kg m2 - Patients with a known history of allergy or contraindication to any of the drugs to be used in the study

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• maintenance of anesthesia
Types used to maintain anesthesia

Locations
Country Name City State
Turkey Zonguldak Bülent Ecevit University Medicine Faculty Zonguldak Kozlu

Sponsors (1)
Lead Sponsor Collaborator
Zonguldak Bulent Ecevit University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary quality of recovery-40 questionnaire measurement of recovery quality in the first 24 hours after extubation up to 24 hour after surgery
Secondary postoperative complications complications that may occur in the postoperative period up to 24 hour after surgery
Secondary duration of extubation time between the last suture and extubation end of the surgery
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