A clinical study to compare pain relief for block performed before and after surgery in patients having surgeries in the jaw
Not Applicable
- Conditions
- Health Condition 1: S02- Fracture of skull and facial bones
- Registration Number
- CTRI/2019/11/021902
- Lead Sponsor
- SRM Medical College Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with ASA Physical Status I and II posted for fractures of mandible
Exclusion Criteria
1. All patients with ASA Physical Status III and above
2. Patients who refuse to participate in the study
3. Patients who are allergic to amide local anaesthetics
4. Patients who are pregnant
5. Patients with chronic cardiac, renal or hepatic condition
6. Patients with coagulation abnormalities
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of postoperative analgesiaTimepoint: within 24 hours of surgery
- Secondary Outcome Measures
Name Time Method Haemodynamic parametersTimepoint: The heart rate,and blood pressure intraoperatively will be observed.;Morphine consumptionTimepoint: The total consumption of morphine in the first 24 hours in PCA pump will be recorded