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Evaluation of the Combined Effect of Preoperative Patient Education and Gradual Extubation on Hemodynamic Stability and Recovery Quality in Rhinoplasty Surgery

Evaluation of the Combined Effect of Preoperative Patient Education and Gradual Extubation on Hemodynamic Stability and Recovery Quality in Rhinoplasty Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210222050463N3
Enrollment
60
Registered
2026-05-04
Start date
2026-06-27
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Gradual Extubation in Rhinoplasty Surgery.

Interventions

Intervention group: Phase 1 (Patient Selection and Pre-operative Preparation): Eligible patients will be selected. In the pre-operative session, the anesthesia procedure will be explained to the patie

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Age range: 18-35 years Physical status: American Society of Anesthesiologists (ASA) Class I-II Candidates for general anesthesia and endotracheal intubation Willingness to participate in the study

Exclusion criteria

Exclusion criteria: Physical status: American Society of Anesthesiologists (ASA) Class III or higher History of cognitive and psychiatric disorders (dementia, severe depression) Patients taking specific medications (e.g., anxiolytics, sedatives, antipsychotics, or antiepileptics) Body Mass Index (BMI) greater than 30 kg/m² History of difficult airway (Cormack-Lehane grade 2 or higher) or more than one intubation attempt Unwillingness to participate in the study

Design outcomes

Primary

MeasureTime frame
Hemodynamic parameters (blood pressure, heart rate, oxygen saturation). Timepoint: Before induction of anesthesia, 2. At the end of the procedure (before extubation), 3. One minute after extubation, 4. Three minutes after extubation. Method of measurement: Monitoring device in the operating room and recovery room.;Extubation Quality Scale. Timepoint: After Extubation. Method of measurement: Psychometrically validated researcher-made checklist.;Time to achieve the best Aldert score in minutes (including: activity, breathing, circulation, alertness, skin color). Timepoint: In the recovery unit. Method of measurement: Psychometrically validated researcher-made checklist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNooshin Sarvi- Sarmeydani

Ahvaz University of Medical Sciences

sarvi.n@ajums.ac.ir+98 61 3314 0000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026