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Effect of intravenous warm fluids on surgery shivering and core temperature in patients undergoing abdominal surgery

Investigation the effect of intravenous warm fluids on surgery shivering and core temperature in patients undergoing abdominal surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201601163311N2
Enrollment
70
Registered
2016-04-10
Start date
2015-12-01
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

surgery shivering. Hypothermia following anaesthesia

Interventions

Intervention 1: Intervention group: Patients in intervention group will received warm fluids (Ringer serum) 38 Celsius after warming and checking by Warmer. Intervention 2: Control group: Patients in
Prevention
Intervention group: Patients in intervention group will received warm fluids (Ringer serum) 38 Celsius after warming and checking by Warmer
Control group: Patients in control group will received fluids (Ringer serum) with temperature same as room

Sponsors

Kurdistan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients undergoing abdominal surgery; Volunteer for research participation; Non-emergency surgery; Term (37-42 week) pregnancy in cesarean surgery; General or spinal anesthesia; Lack of corticosteroids; NSAIDs; Lack of Magnesium sulfate; Lack of Antihypertensives drugs; Lack of Endocrine disease; Lack of Vascular disease; Lack of Thyroid disease; Lack of Hypertension; Lack of Fever; Lack of addiction Exclusion criteria: Blood transfusion during surgery; Hypotension during surgery; Patient dissuasion

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Shivering. Timepoint: Just entering recovery room and after 30 Min. Method of measurement: CROSSLEY AND MAHAJAN Scale.;Core temperature. Timepoint: Just entering recovery room and after 30 Min. Method of measurement: Tympanic Thermometer.

Secondary

MeasureTime frame
SPO2, Systolic and Diastolic pressure, Pulse. Timepoint: Just entering recovery room and after 30 Min. Method of measurement: Pulse oximeter, Sphygmomanometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSina Valiee

Kurdistan University of Medical Sciences

sinavaliee@yahoo.com+98 87 3316 7525

Outcome results

None listed

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