Skip to content

Comparison of patient extubation after septoplasty operation

Comparison of patient extubation in sitting versus supine position after septoplasty operation in 501 AJA hospital.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110103005536N7
Enrollment
60
Registered
2020-07-01
Start date
2015-07-07
Completion date
Unknown
Last updated
2020-07-13

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

Conditions

septoplasty. Deflection or deviation of septum

Interventions

Intervention 1: Intervention group: Patients using the Simple Random Sampling sampling method are divided into two groups using black and white cards (30 people per group). In one group, after the ope

Sponsors

Artesh University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: patient in 20-60 years old ASA 1

Exclusion criteria

Exclusion criteria: patient with ASA II, III, IV hematologic disorders cervical rheumatoid arthritis

Design outcomes

Primary

MeasureTime frame
Position of extubation. Timepoint: during the intervention. Method of measurement: observation. this parameter evaluates in two position: supine and sitting.

Secondary

MeasureTime frame
Systolic blood pressure. Timepoint: during the intervention. Method of measurement: monitoring of patient blood pressure.;Heart rate. Timepoint: during the intervention. Method of measurement: monitoring of patient heart rate.;Arterial oxygen saturation. Timepoint: during the intervention. Method of measurement: monitoring of patient arterial oxygen saturation.;Laryngospasm. Timepoint: during the intervention. Method of measurement: clinical.;Agitation. Timepoint: during the intervention. Method of measurement: Richmond agitation sedation scale (RASS).;Oral suction. Timepoint: during the intervention. Method of measurement: Count the number of times you need to suction with the device.;Age. Timepoint: before start of intervention. Method of measurement: patient identification card.;Gender. Timepoint: Before start of intervention. Method of measurement: based on the phenotype.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mohamadreza Rafiei

Artesh University of Medical Sciences

mo_rafiei@armyums.ac.ir+98 31 3261 6302

Outcome results

None listed

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