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Evaluating of suppressive effect of remifentanil on responses to the endotracheal tube during emergence from general anesthesia.

Effect of low-dose remifentanil on responses to the endotheracheal tube during emergence from general anesthesia on patients undergoing elective nasal surgery in emam khomeyni hospital of awaz

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201103186089N1
Enrollment
Unknown
Registered
2011-10-28
Start date
2010-06-07
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

Condition 1: heart rate. Condition 2: systolic blood pressure. Condition 3: cough. Condition 4: nausea-vomiting. Symptoms and signs involving the circulatory and respiratory systems Abnormal blood-pressure reading, without diagnosis Cough Nausea and vomiting

Interventions

Intervention 1: 0.02 micro/kg/min of remifentanil in treatment group 1. Intervention 2: use of plasbo (normal salin) in control group. Intervention 3: 0.05 micro/kg/min of remifentanil in treatment gr
Prevention
0.02 micro/kg/min of remifentanil in treatment group 1
use of plasbo (normal salin) in control group
0.05 micro/kg/min of remifentanil in treatment group 2

Sponsors

Ahvaz Jundishapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients aged 18-40 years ; ASA classI; undergoing nasal surgery. Exclusion criteria: patients under 18 years; above 40 years; history of respiratory infection ; history of irritable airway; difficult intubation; G-E reflux; post-op PONV;motion sickness.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Heart rate,systolic blood pressure,cough,nausea-vomiting. Timepoint: from end of surgery to 4 min after extubation. Method of measurement: noninvasive blood pressure monitoring, pulse oxymeter, scoring system of coughing & nausea-vomiting.—

Secondary

MeasureTime frame
The time of extubation ,arrive to recovery and discharge from recovery. Timepoint: from end of surgery to discharge from recovery. Method of measurement: cornometer.—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mohamadreza Gousheh

Ahvaz Jundishapur University of Medical Sciences

mgoushe@gmail.com+98 61 1222 2114

Outcome results

None listed

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