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Comparison the effect of two methods of warming on the physiological indices during and after laparoscopic abdominal surgery at the Alzahra Hospital of Isfahan in 2017

Comparison the effect of two methods of warming on the physiological indices during and after laparoscopic abdominal surgery at the Alzahra Hospital of Isfahan in 2017

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017041533435N1
Enrollment
96
Registered
2017-05-16
Start date
2017-03-08
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

hypothermia and Shivering. Other complications of anaesthesia

Interventions

Intervention 1: Patients immediately after induction of anesthesia under a forced air system with maximum temperature will be 45 ° C. Intervention 2: Warming IV fluids (38 ° C) is recommended immediat
Prevention
Patients immediately after induction of anesthesia under a forced air system with maximum temperature will be 45 ° C.
Warming IV fluids (38 ° C) is recommended immediately after induction of anesthesia
Control group receive routine care.

Sponsors

Vice chancellor for research, Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria: satisfaction; no underlying disease (hypothyroidism, hyperthyroidism, diabetes and hypertension) and cardiovascular disease; no fever; aged between 18 and 65 years; surgery time up to 2 hours; no received Corticosteroids and non-steroidal anti-pain; lack of infection; ASA = I - II; BMI = 18.5 - 38. The exclusion criteria: the need for open surgery or return the patient to the operating room; and said heat felt by the patient in recovery; need for blood transfusions during and after surgery; intra-abdominal infections; blood loss during surgery more than 1 liter; Sensitivity to anesthetic drugs; get more than 5 liters of intravenous fluids during surgery; temperature more than 37.5 or less than 36.5 prior to surgery; the need for cardiopulmonary resuscitation during surgery; intraoperative hemodynamic changes include a severe drop in blood pressure and pulse; using humid and warm CO2 gas for pneumoperitoneum.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Core body temperature. Timepoint: Before induction of anesthesia, immediately after induction of anesthesia and then every 15 minutes until 30 minutes after the end of surgery. Method of measurement: Tympanic thermometers.;Blood pressure. Timepoint: Before induction of anesthesia, immediately after induction of anesthesia and then every 15 minutes until 30 minutes after the end of surgery. Method of measurement: Blood Pressure Monitor (monitoring vital signs).;Pulse. Timepoint: Before induction of anesthesia, immediately after induction of anesthesia and then every 15 minutes until 30 minutes after the end of surgery. Method of measurement: Pulse oximetry (monitoring vital signs).;Respiratory rate. Timepoint: Before induction of anesthesia, immediately after induction of anesthesia and then every 15 minutes until 30 minutes after the end of surgery. Method of measurement: Counting (monitoring vital signs).;Oxygen saturation. Timepoint: Before induction of anesthesia, immediately after induction of anesthesia and then every 15 minutes until 30 minutes after the end of surgery. Method of measurement: Pulse oximetry (monitoring vital signs).;Shivering. Timepoint: after surgery. Method of measurement: Visual assessment scale.

Secondary

MeasureTime frame
Duration of anesthesia. Timepoint: after suegery. Method of measurement: Since the induction of anesthesia until extubation.;Intravenous fluids. Timepoint: after suegery. Method of measurement: Observation.;Duration of surgery. Timepoint: after suegery. Method of measurement: from making the surgical incision to skin closure and dressing.;Pneumoperitoneum time. Timepoint: after suegery. Method of measurement: Since the introduction of gas into the abdomen until removing it from the abdomen.;The volume of carbon dioxide input. Timepoint: after suegery. Method of measurement: Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFereshteh Baradaran Fard

Isfahan University of Medical Sciences

baradaranfard.f@gmail.com+98 31 3792 7510

Outcome results

None listed

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