A study to see the additive epidural analgesic effect of two drugs dexmedetomidine & fentanyl
Phase 1
- Conditions
- Health Condition 1: G890- Central pain syndrome
- Registration Number
- CTRI/2020/05/025233
- Lead Sponsor
- Ptjnm medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients undergoing lower thoracic (below T8)& lumbosacral spine fixation
Exclusion Criteria
1.Refuse to participate, 2.chronic pain syndrome, 3. cardiac diseases,4.hematological disease, 5.psychiatric disease,6.allergy to local anaesthetic, 7.upper thoracic & 8.cervical spine surgery,9.tubercular spine
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Analgesia using VISUAL ANALOG SCORE.Timepoint: 1year
- Secondary Outcome Measures
Name Time Method Patients satisfaction <br/ ><br>Ramsay sedation score <br/ ><br>Heart rate <br/ ><br>Blood pressure <br/ ><br>Side effectsTimepoint: 24 hours