Comparison of 2 different doses of dexmedatomidine with 0.5 percent levobpivacaine for post operative analgesia

Not yet recruiting

• Conditions: Other specified injuries of elbowand forearm,

• Registration Number: CTRI/2020/05/025249
• Lead Sponsor: CHETTINAD HOSPITAL AND REASERCH INSTITUTE

Brief Summary

Patients who are posted for elective and emergency upperlimb procedures

Patients who are classified under american society of anaesthesiologists,who comes under ASA-1 and ASA-2

For elective surgeries adequate NPO status of six hours is maintained preoperatively

T.Dizepam 5mg and T.Rantac150 mg is given preoperative night before surgery

For emergency procedure NPO status of six hours is followed

A total number of 56 patients are allocated randomly using computer generated code,Group 50 receives 29 ml of 0.5% levobupivacaine groupD75 recieves 75 microgram of dexmedatomidine and 29 ml of 0.5 percent levobupivacaine

Motor onset and sensory onset are recorded

Surgeries done only under block

Intraoperative and post operative hemodynamic variables are recorded for each patient

Patient shifted to surgical ICU after the procedure and post operatively patient is monitored

If patient have VAS score more than 3/10 then rescue analgesia is given with tramadol 100 mg

Detailed Description

Not available

Study Timeline

• Study Start: 2020-05-20
• Last Update Posted: 2020-05-20

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 56

Inclusion Criteria

All ASA-1 AND ASA-2 patients undergoing either elective or emergency upperlimb surgical procedure.

Exclusion Criteria

Pediatric patients Geriatric patients(age more than 70 years) Patients with known comorbities(diabetes,hypertension,asthma,seizure disorder,hypothyroidism) patients who are allergic to local anaesthetic drugs Patients who are not not willing for surgical procedure under regional anaesthesia.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
every 30 min till the onset of pain	every 30 min after injecting drug till the onset of pain

Secondary Outcome Measures

Name	Time	Method
effect on hemodynamics	onset and duration of of sensory and motor blokade

Trial Locations

Locations (1)

Chettinad hospital and research institute; 🇮🇳 Kancheepuram, TAMIL NADU, India

Chettinad hospital and research institute

🇮🇳Kancheepuram, TAMIL NADU, India

DrASHOK KULASEKHAR

Principal investigator

9840498420

ashokk_dr@yahoo.com