Ain Shams University
Cairo, Egypt
Location status: Recruiting
NCT Number: NCT07154849
The aim and purpose of this study is to compare the efficacy of intravenous hydrocortisone and intravenous dexmedetomidine for prevention and treatment of postoperative shivering after general anesthesia for abdominal surgeries.
Interested in participating?
Request Info18 year–65 year
All sexes
Interventional
Phase 4
Cairo, Egypt
Location status: Recruiting
All patients will be assessed preoperatively by careful history taking, full physical examination, and laboratory evaluation. An informed written consent will be taken from every patient just before the surgery.
Patients will be divided into two groups:
Approximately 30 minutes before the anticipated completion of surgery, the study drugs will be given to the two groups.
Ephedrine (10 mg IV bolus) will be given for hypotension (systolic blood pressure < 80 mmHg) and atropine (0.5 mg IV bolus) will be given for bradycardia (HR < 50 BPM).
At the end of surgery, extubation will be done and patients will be transferred to the post-anaesthesia care unit (PACU), for further monitoring.
Core temperature will be measured directly after endotracheal intubation and every 15 minutes during the operation. Upon transferal of the patient to the post-anesthesia care unit (PACU), core temperature will be measured and shivering will be graded from (0-3) according to the shivering scale validated by Crossley and Mahajan as follows: 0 = no shivering, 1 = mild fasciculation of the face or neck, 2 = visible tremor involving more than one muscle group, 3 = gross muscular activity involving the entire body.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
any patient undergoing abdominal surgery ASAI or II.
-
Exclusion criteria
received 2mg/kg.
received 1 µg/kg
Time frame: 30 minutes
In this study it was targeted to assess the efficacy of hydrocortisone and dexmedetomidine in reducing shivering that occur post operatively.
Contact information is provided by the study sponsor or research team.
Ain Shams University
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07511491
Cesarean Section, Intravenous
Tanta, El-Gharbia, Egypt
View Trial DetailsNCT07489742
Intravenous, Lozenge
Tanta, El-Gharbia, Egypt
View Trial DetailsNCT04730609
Dose Finding Study, Shivering
Rochester, Minnesota, United States
View Trial DetailsNCT06708169
Shivering, Spinal Anesthesia
Seoul, Jongno-gu, South Korea
View Trial Details