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Evaluation of the Effect of Hypothermia Prevention Program in Children Undergoing Orthopedic Surgery

Evaluation of the Effect of Hypothermia Prevention Program on, Recovery Time, Shivering and Hemodynamic Status in Pediatric Undergoing Orthopedic Surgery Under General Anesthesia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200501047254N2
Enrollment
60
Registered
2022-02-23
Start date
2022-03-06
Completion date
Unknown
Last updated
2022-03-08

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

Conditions

Condition 1: Hypothermia of newborn. Condition 2: Hypothermia. Hypothermia of newborn

Interventions

Intervention 1: Control group: Performing routine care in the operating room to maintain the patient's temperature and prevent hypothermia. Intervention 2: Intervention group: In this group, heated so

Sponsors

Gonabad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 18 Years

Inclusion criteria

Inclusion criteria: Children undergoing surgery with a minimum time of 30 minutes Age 3 to 18 years The patients who are candidate for general anesthesia Patients with ASA class 1 and 2 Body temperature 36.5 to 37 ° C No drug addiction Reluctance to continue participating in the project

Exclusion criteria

Exclusion criteria: Occurrence of any condition that affects the patient's normal course of anesthesia and surgery, such as excessive bleeding and cardiac arrest during surgery Significant decrease in blood pressure during surgery (20% decrease in blood pressure compared to before anesthesia) Temperatures above 37.5 ° C or below 36 ° C before surgery Receiving blood and blood products during surgery Take corticosteroids Receiving non-steroidal analgesics and magnesium sulfate Prohibition to control body temperature through the tympanic membrane Receiving drugs other than fentanyl during surgery

Design outcomes

Primary

MeasureTime frame
Hypothermia. Timepoint: The measurement of the variable in eight shifts will include the following: 5 minutes before the start of anesthesia, 5 minutes after induction of anesthesia and one minute before the start of surgery, 30 minutes after the start of surgery, after the end of surgery, at the beginning of recovery, 30 minutes and 1 hour after transferring the patient to recovery will be monitored. Method of measurement: Tympan thermometer.;Hemodynamic status. Timepoint: The measurement of the variable in eight shifts will include the following: 5 minutes before the start of anesthesia, 5 minutes after induction of anesthesia and one minute before the start of surgery, 30 minutes after the start of surgery, after the end of surgery, at the beginning of recovery, 30 minutes and 1 hour after transferring the patient to recovery will be monitored. Method of measurement: Anesthesia monitor.;Shivering. Timepoint: The measurement of the variable at the beginning of recovery, 30 minutes and 1 hour after transferring the patient to recovery will be monitored. Method of measurement: Mahajan and Crossley criteria will be used to evaluate the incidence of postoperative shivering. The number zero indicates the patient without shivering, the number 1 = mild shivering (hair straightening), the number 2 = moderate shivering (muscle tremors visible in one group of muscles), the number 3 = severe shivering) muscle tremors in more than one group of Muscles but not in the whole body (generalized) and the number 4 - will show very strong vibration (generalized body vibration).;Recovery time. Timepoint: From the moment of arrival until the patient is discharged from recovery. Method of measurement: Timer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Pouladkhay

Gonabad University of Medical Sciences

pouladkhay.fatemeh@gmail.com+98 51 5722 3028

Outcome results

None listed

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