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Comparison of propofol or isofluran anesthesia for sinus surgery

Comparison of surgical condition and bleeding during propofol or isofluran anesthesia for endoscopic sinus injury

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201102081138N7
Enrollment
44
Registered
2011-03-14
Start date
2010-06-13
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Chronic Sinusitis. Chronic sinusitis, unspecified

Interventions

Intervention 1: Group A) propofol (50/mg/kg/min) + remifentanyl (0/1 mg/kg/min) group. Intervention 2: Group B) Insofluran group (0-0/6%).
Treatment - Drugs
Group A) propofol (50/mg/kg/min) + remifentanyl (0/1 mg/kg/min) group
Group B) Insofluran group (0-0/6%)

Sponsors

Guilan University of Medical Sciences, Vice Chancellor for Research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients candidated for elective endoscopic sinus surgery (15-45yr); ASA class I,II; Patients with completely treated nose and sinus infections Exclusion criteria: History of hemorrhagic disease; Seizure; Drugs that affect on the surgical homeostasis; Anemia (Hb <10); Poor controlled cerebrovascular accident; History of significant CAD; Arrhythmia; Liver or kidney dysfunction; Electrolyte or metabolic abnormalities; COPD; Severe asthma or other severe respiratory disease; History of PUD; Pregnancy

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Surgical field condition. Timepoint: Every 15 minutes. Method of measurement: With table.

Secondary

MeasureTime frame
Intraoperative bleeding percent. Timepoint: Every 15 minutes Intraoperatively. Method of measurement: Maximum allowable blood loss formula.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Sudabeh Haddadi

Guilan University of Medical Sciences

So_haddadi@gums.ac.ir+98 13 1222 5242

Outcome results

None listed

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