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se of 2-chloroprocaine by adding fentanyl and dexmedetomidine in short duration orthopaedic surgeries

Phase 4
Conditions
Health Condition 1: S80-S89- Injuries to the knee and lower leg
Registration Number
CTRI/2020/07/026388
Lead Sponsor
Sri Venkateswara Institute of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Patients of American society of Anesthesiologists physical status grade 1 and 2

2. Patients of age group between 20 to 65 years

3. patients posted for elective lower limb orthopaedic surgeries with duration of 1.5 to 2 hrs

Exclusion Criteria

1. Patients who are not willing to participate in the study.

2. Patients who do not give consent for spinal anaesthesia.

3. H/o spinal surgeries.

4. H/o coagulation and bleeding disorders.

5. Local site infections.

6. H/o hypersensitivity to study drugs.

7. H/o uncontrolled HTN and DM & H/o CAD.

8. Increased serum creatinine and liver enzymes:

2-3 times of normal.

9. H/o neuropsychiatric disorders and communication problems

10. Patients who cannot understand visual analog scale (VAS) measurements.

11. Pregnant women and lactating mothers.

12. Height- <140 cm & BMI > 35 Kg/m2.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Duration of analgesiaTimepoint: Time of the first analgesic request
Secondary Outcome Measures
NameTimeMethod
1.Onset of sensory block <br/ ><br>2.Onset of motor block <br/ ><br>3.Height of the sensory block <br/ ><br>4.Duration of sensory block <br/ ><br>5.Duration of motor block <br/ ><br>6.Regression time below L1 <br/ ><br>7.VAS score of pain <br/ ><br>8.VAS score of patient satisfaction <br/ ><br>9.Adverse hemodynamic effects during the study period <br/ ><br> <br/ ><br>Timepoint: 0,3 min, 6 min, 9 min, 12 min, 15 min, 30 min, 45 min, 60 min, 2 hrs, 3 hrs and 4 hrs after injection of study drug. <br/ ><br>
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