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Comparison effect of warm serum and Hot air Radiant on post operative complication in cesarean surgery

Comparison effect of warm serum and Hot air Radiant on prevention of Headache - nausea and vomiting after cesarean surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017020232361N1
Enrollment
75
Registered
2017-05-27
Start date
2017-05-05
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

surgical complication of cesarean section. Other surgical procedures

Interventions

Intervention 1: Control group: receiving Serum with Equal operation room temperature and without Hot air Radiant. Intervention 2: The first intervention group: This group of patients recived warm int
Treatment - Drugs
Prevention
Control group: receiving Serum with Equal operation room temperature and without Hot air Radiant.
The first intervention group: This group of patients recived warm intravenous serum(37.5 degrees) For complet time of surgery and recovery.Heating serum is by Hot Line Manufacturing Co. Hotline® Blood
Patients in the intervention group II: This group of similar patients in the control group, except that after entering the recovery room warm air radiation (by heating warm-med making Turkey) to the e

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria include: age between 20–60 years old; undergoing cesarean surgery under spinal anesthesia;and duration of surgery between ./5 and 2 h. Exclusion criteria include: Having a history of thyroid disease, use of anticholinergic drugs, patients with infection in surgical location, diabetic, emergency surgery; Having a history of headaches, Patients with very high weight BMI>35, Body Temperature>38 or <36, A history of motion sickness, Received blood products during surgery and emergency surgery.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Bleeding. Timepoint: Intraoperative. Method of measurement: Weight change gases, and Long gases and blood volume within the botel suction.;Core temperature. Timepoint: Every 15 minutes , before induction of anesthesia to the end of Recovery. Method of measurement: Using a tympanic thermometer.;Blood pressure. Timepoint: Before Surgery then every 15 minutes to the end of the recovery. Method of measurement: Using cardiac pressure monitoring device.;Shivering. Timepoint: After the intervention in recovery. Method of measurement: Three-point scale of shivering.;Anxiety. Timepoint: Before Surgery- after surgery and then 6-12 and 24 h after surgery. Method of measurement: spielberger anxiety questionnaire.

Secondary

MeasureTime frame
Nausea and vomiting. Timepoint: Since his arrival in recovery every six hours in first 24h. Method of measurement: Based on the VAS scale.;The duration of anesthesia. Timepoint: During the injection -end of operation and then every 15 min to complet motor and sensory recovery. Method of measurement: base on Bromage scale.;Pain. Timepoint: every 6h and before analgesics druge Prescription. Method of measurement: base on VAS scale.;Anxiety. Timepoint: before operation- post operation- 6,12 and 24 h after operation. Method of measurement: base on Spielberger questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHojjat Torkmandi

Semnan University of Medical Sciences

hojjat.or@gmail.com+98 23 3365 4191

Outcome results

None listed

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