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Evasluation of the effect of remifentanil on postoperative shivering after ambulatory gynecologic procedures

Comparison of Postoperative Shivering after Remifentanil-Propofol versus fentanyl-propofol Intravenous Anesthesia in patients undergoing ambulatory Gynecologic Procedures

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015043011700N7
Enrollment
100
Registered
2015-08-20
Start date
2014-12-22
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

Postoperative shivering. R68.0 Hypothermia, not associated with low environmental temperature ,hypothermia (due to)(of):anaesthesia (T88.5)

Interventions

Intervention 1: Interventional group: In remifentanil group, general anesthesia will induce with midazolam0.05 mg/kg IV, propofol 2-2.5 mg/kg IV and follow by infusion of propofol 5-10µg/kg/h.Then,rem
Prevention
Treatment - Drugs
Interventional group: In remifentanil group, general anesthesia will induce with midazolam0.05 mg/kg IV, propofol 2-2.5 mg/kg IV and follow by infusion of propofol 5-10µg/kg/h.Then,remifentanil 1 µg/k
Control group: In group fentanyl (group F)general anesthesia will induce with midazolam0.05 mg/kg IV, propofol 2-2.5 mg/kg IV and follow by infusion of propofol 5-10µg/kg/h .Then, fentanyl 1 µg/kg IV

Sponsors

Tabriz azad Islamic University ,faculty of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
17 Years to 52 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with American Society of Anesthesiology (ASA) physical status I or II; patients scheduled for ambulatory gynecologic procedures Exclusion criteria: patients with ASA class III or higher; patients with cardiopulmonary diseases; Preoperative fever; use of any anti pyretic or anti-inflammatory medication; any surgery time longer than 2 hours

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of postoperative shivering. Timepoint: in recovery every 15 minutes until discharge from recovery. Method of measurement: Crossly and Mahjon five-point scoring system.

Secondary

MeasureTime frame
Pain. Timepoint: in recovery room every 15 minutes until discharge from recovery. Method of measurement: visual analog score.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarnaz Moslemi

Research Center, Tabriz University of Medical Sciences

moslemifa@gmail.com+98 41 3553 9161

Outcome results

None listed

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