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Comparison of two anesthesia methods, sevoflurane fentanyl and propofol fentanyl, on the severity of cough and laryngospasm in orthopedic surgeries under one hour.

Comparison of two anesthesia methods, sevoflurane fentanyl and propofol fentanyl, on the severity of cough and laryngospasm in orthopedic surgeries under one hour.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20231014059718N1
Enrollment
148
Registered
2024-02-03
Start date
2024-01-21
Completion date
Unknown
Last updated
2024-03-06

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

Conditions

Respiratory system problem. Other postprocedural complications and disorders of respiratory system, not elsewhere classified

Interventions

Intervention 1: Intervention group 1: 100 mcg per kilogram of body weight will receive propofol for induction of anesthesia. Intervention 2: Intervention group 2: will receive sevoflurane with MAC=2 f

Sponsors

Bandare-abbas University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Age 18 to 75 Consent to participate in the study

Exclusion criteria

Exclusion criteria: Heart and kidney diseases Hemodynamic instability Drug abuse

Design outcomes

Primary

MeasureTime frame
Severity of cough. Timepoint: During the operation and after casteob and fifteen minutes later and half an hour and an hour later. Method of measurement: Aldrete score.;Laryngospasm. Timepoint: During the operation and after casteob and fifteen minutes later and half an hour and an hour later. Method of measurement: Aldrete score.;Oxygen saturation percentage of arterial blood. Timepoint: During the operation and after casteob and fifteen minutes later and half an hour and an hour later. Method of measurement: Pulse oximeter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Majid vatankhah

Bandare-abbas University of Medical Sciences

hormozgan91@yahoo.com+98 76 5224 1819

Outcome results

None listed

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