Shivering Clinical Trial
Official title:
Prophylactic Paracetamol or Dexamethasone for Post-spinal Anesthesia Shivering in Patients Undergoing Non-obstetric Surgeries: a Randomized Controlled Trial
Verified date | September 2018 |
Source | Ain Shams University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study was conducted to evaluate the effects of a prophylactic dose of oral paracetamol on shivering compared with prophylactic intravenous infusion (IVI) dexamethasone in patients undergoing non-obstetric surgeries under spinal anesthesia.
Status | Completed |
Enrollment | 300 |
Est. completion date | August 31, 2018 |
Est. primary completion date | August 31, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility |
Inclusion Criteria: - • on 300 patients aged 18-60 years - of the American Society of Anesthesiologists (ASA) physical status I or II - underwent non-obstetric surgeries under spinal anesthesia. A written informed consent was obtained from all patients to participate in the study. Exclusion Criteria: - • Patient`s refusal, - duration of surgery more than 120 min, - obesity with body mass index (BMI) >35 kg/m2, - generalized infection or localized infection at level of blockade, - neurologic disease, - coagulation disorder, - patients with hypo- or hyperthyroidism, - cardiopulmonary disease, - psychological disorders, - a need for blood transfusion during surgery, - an initial body temperature >38.0C or <36.0C, - a known history of alcohol or substance abuse, - or receiving vasodilators, or medications likely to alter thermoregulation |
Country | Name | City | State |
---|---|---|---|
Egypt | Ibrahim Mamdouh Esmat | Heliopolis | Cairo |
Lead Sponsor | Collaborator |
---|---|
Ain Shams University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Total participants received pethidine for treatment of post-spinal shivering in the three groups till 20 minutes after the end of the procedure (in the recovery room) | Total participants received pethidine for treatment of post-spinal shivering in the three groups till 20 minutes after the end of the procedure (in the recovery room) | Till 20 minutes after the end of the procedure (in the recovery room) |
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