Comparing pain relieving efficacy of oral clonidine and oral pregabalin given pre-emptively to patients planned for upper limb surgeries under regional anesthesia
Not Applicable
- Conditions
- Health Condition 1: null- Patients posted for upper limb surgeries under supraclavicular block having ASA Grade I-II.
- Registration Number
- CTRI/2018/08/015353
- Lead Sponsor
- Dr RPGMC Kangra at Tanda
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Scheduled for upper limb surgeries under supraclavicular block.
2. ASA Grade I-II.
3. BMI 18.5-29.9.
Exclusion Criteria
1. Patientâ??s refusal for block
2. Patients with known drug allergy to study
3. Patients who have taken analgesics 48hrs before
4. Use of antiepileptics drugs
5. Hepatic and renal pathologies affecting drug clearence
6. History of long term usage of NSAIDs and opioid analgesics
7. Patient in whom the block effect will be partial and will require supplementary analgesic
8. Diabetes mellitus and other neuropathic disorders
9. Any contraindications for peripheral nerve blocks
10. Coagulopathy disorders
11. Psychiatric disorders
12. Addiction to any drug
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To study and compare block characteristics and rescue analgesic requirement with pre-emptive oral clonidine and oral pregabalin.Timepoint: 24hours
- Secondary Outcome Measures
Name Time Method To study and compare post-operative sedation and patient satisfaction.Timepoint: 24hours