Perioperative Continuous Intravenous Lidocaine Infusion For Evaluation Of Postoperative Recovery Profile In Orthognathic Surgery.
Phase 2
- Conditions
- Bimaxillary orthognathic surgery.00
- Registration Number
- IRCT201308141674N8
- Lead Sponsor
- Vice-Chancellery of Research and Technology, Shiraz University Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Patients with no history of systemic disease and without taking any analgesic medications criteria that were willing to cooperate in this study were enrolled; and Exclusion criteria included known allergy to the study drugs; Serious adverse drug reaction to amide local anaesthetics; hepatic and renal dysfunction ; patients with heart block including second or third degree (without pacemaker) ; Severe sinoatrial block (without pacemaker) ; Use of opioid or analgesics 3 days before the study; Acute Porphyria; Accelerated idioventricular rhythm ; Bradycardia ; and Patients who did not sign the informed consent.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Heart rate and blood pressure monitoring. Timepoint: During operation and end of surgery. Method of measurement: Heart rate and blood pressure measuring device.;The severity of postoperative pain. Timepoint: In the recovery room. Method of measurement: Visual analog scale.;The amount of intraoperative bleeding. Timepoint: During surgery and in the recovery room. Method of measurement: Cc in volume suction and Surgical gauze counting.
- Secondary Outcome Measures
Name Time Method