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Study of the effects of various airway preservation methods on anesthesia complications

Comparison of laryngeal mask and tracheal tube on duration and complications of anesthesia in reconstructive hand surgery patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240721062495N1
Enrollment
90
Registered
2024-07-30
Start date
2024-08-10
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Examination of the airway during anesthesia.

Interventions

Intervention 1: Intervention group: Tracheal tube. Intervention 2: Intervention group: Laryngeal mask.

Sponsors

Khoram-Abad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients undergoing hand reconstruction surgery Patients aged 18-60 years Patients with ASA class ?-,? Patients' consent to participate in the study

Exclusion criteria

Exclusion criteria: Congenital diseases of the jaw and face Pregnant patients Abnormal airway anatomy Gastric aspiration during surgery Hemodynamic changes such as increased blood pressure

Design outcomes

Primary

MeasureTime frame
Determining and comparing the duration and complications of anesthesia over time after using laryngeal mask and tracheal tube in patients undergoing hand reconstruction surgery. Timepoint: Laryngeal mask - tracheal tube. Method of measurement: observasion.;Measurement time. Timepoint: Before anesthesia, 10 and 20 minutes after anesthesia, recovery room. Method of measurement: observation.;Age. Timepoint: Number of years of life. Method of measurement: interview.;Sore throat. Timepoint: Recovery. Method of measurement: Feeling of pain by the patient (Likert scale) Visual Analogue Scale.;Duration of anesthesia. Timepoint: before the time of intervention until the end of anesthesia. Method of measurement: Stopwatch.;Systolic blood pressure. Timepoint: Before anesthesia, 10 and 20 minutes after surgery, recovery room. Method of measurement: Medical sphygmomanometer.;Diastolic blood pressure. Timepoint: Before anesthesia, 10 and 20 minutes after surgery, recovery room. Method of measurement: Medical sphygmomanometer.;Heart rate. Timepoint: Before anesthesia, 10 and 20 minutes after surgery, recovery room. Method of measurement: Anesthesia monitor device.;Breathing rate. Timepoint: Before anesthesia, 10 and 20 minutes after surgery, recovery room. Method of measurement: Anesthesia monitor device.;Blood oxygen saturation. Timepoint: Before anesthesia, 10 and 20 minutes after surgery, recovery room. Method of measurement: Anesthesia monitor device (Pulse oximeter).;Occurrence of cardiac arrhythmia. Timepoint: Before anesthesia, 10 and 20 minutes after surgery, recovery room. Method of measurement: Anesthesia monitor device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKian Karami

Khoram-Abad University of Medical Sciences

kiankarami23@gmail.com+98 66 3332 4132

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026