General AnesthesiaNCT06423313
Effects of Anesthesia Type on QoR-40
An observational study of General Anesthesia and İnhalation Anesthetics, run by Zonguldak Bulent Ecevit University at 1 site in Turkey (Türkiye).
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). Read more about this study
- Who is it for?
- Ages 18 to 65 yearsHealthy volunteers can take part
- Conditions the study is for
- General Anesthesia, İnhalation Anesthetics, Quality of Recovery
- What is being tested?
- maintenance of anesthesia
- Type of treatment
- Surgery or procedure
- How many people
- 1 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 1 May 2024to 31 Dec 2024
- How long will I take part?
- 1 Day
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: The study will include intubated patients who will undergo septorhinoplasty surgery under general anesthesia, aged 18-65 years, in the American Society of Anesthesiology (ASA) I-II-III risk class.
Who may be able to join
- 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
Who cannot join
- -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
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site
Zonguldak Bülent Ecevit University Medicine Faculty
Zonguldak, Kozlu, 67600
About this study
Official title: The Comparison of Total Intravenous Anesthesia and Inhalation Anesthesia Effects on Postoperative Recovery by Quality of Recovery (QoR-40) in Septorhinoplasty
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).
- Being tested
- maintenance of anesthesia
- Keywords
- total intravenous anesthesia, anesthesia maintenance, inhalation anesthesia, quality of recovery-40
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
maintenance of anesthesiaProcedure or surgery
Types used to maintain anesthesia
| Study group | Role | What they receive |
|---|---|---|
| Group TIVA | Not described Receives: Procedure: maintenance of anesthesia | |
| Group Inhalation | Not described Receives: Procedure: maintenance of anesthesia |
What is being measured
The primary outcome is the main question the study is designed to answer.
quality of recovery-40 questionnaire
measurement of recovery quality in the first 24 hours after extubation with quality of recovery-40 questionnaire. Quality of recovery-40 questionnaire scores range from 40 (extremely poor quality of recovery) to 200 (excellent quality of recovery).
Measured: up to 24 hour after surgery
Secondary outcomes (2)
postoperative complications
complications that may occur in the postoperative period
Measured: up to 24 hour after surgery
duration of extubation
time between the last suture and extubation
Measured: end of the surgery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 May 2024
- Study start1 May 2024
- Primary completion30 Nov 2024
- Study completion31 Dec 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for General AnesthesiaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 1 participants (actual)
- Target duration
- 1 Day
Sponsor and investigators
- Lead sponsor
- Zonguldak Bulent Ecevit University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Çağdaş Baytar, Zonguldak Bulent Ecevit University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06423313
- Sponsor's protocol ID
- 2024/07-1
- Status last verified
- Apr 2025
- First submitted
- 3 May 2024
- Last updated
- 22 Apr 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 22 Apr 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Comparison of Total Intravenous Anesthesia and Inhalation Anesthesia Effects on Postoperative Recovery by Quality of Recovery (QoR-40) in Septorhinoplasty
- ClinicalTrials.gov ID
- NCT06423313
- Acronym / sponsor ID
- 2024/07-1
- Keywords
- total intravenous anesthesia, anesthesia maintenance, inhalation anesthesia, quality of recovery-40
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 1 participants (actual)
- Lead sponsor
- Zonguldak Bulent Ecevit UniversityUniversity, hospital or other
- Study start
- 1 May 2024 (actual)
- Primary completion
- 30 Nov 2024 (actual)
- Study completion
- 31 Dec 2024 (actual)
- First posted
- 21 May 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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).
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 1 Day
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Group TIVA | – | Procedure: maintenance of anesthesia |
| Group Inhalation | – | Procedure: maintenance of anesthesia |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- The study will include intubated patients who will undergo septorhinoplasty surgery under general anesthesia, aged 18-65 years, in the American Society of Anesthesiology (ASA) I-II-III risk class.
Key inclusion criteria (4 listed)
- 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
Key exclusion criteria (7 listed)
- -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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| maintenance of anesthesiaTypes used to maintain anesthesia | Procedure or surgery | Group Inhalation, Group TIVA |
Primary outcome
quality of recovery-40 questionnaire
Time frame: up to 24 hour after surgery
measurement of recovery quality in the first 24 hours after extubation with quality of recovery-40 questionnaire. Quality of recovery-40 questionnaire scores range from 40 (extremely poor quality of recovery) to 200 (excellent quality of recovery).
2 secondary outcomes
postoperative complications
Time frame: up to 24 hour after surgery
duration of extubation
Time frame: end of the surgery
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Apr 2025.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of General Anesthesia and İnhalation Anesthetics, run by Zonguldak Bulent Ecevit University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 22 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
quality of recovery-40 questionnaire (time frame: up to 24 hour after surgery). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Apr 2025; AzTrials last refreshed its copy on 6 Nov 2026.