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Comparison between efficacy of Clonidine and Dexmedetomidine with Levobupivacaine while being used in Spinal Anesthesia for lower limb surgery in Medical College Kolkata

Phase 4
Conditions
Health Condition 1: O- Medical and SurgicalHealth Condition 2: M218- Other specified acquired deformities of limbs
Registration Number
CTRI/2023/09/057773
Lead Sponsor
Dr Anjana Ghosh Dastidar Bose
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Patients scheduled for elective lower limb surgeries under spinal anesthesia during the period of data collection.

Patients with physical status ASA-I and ASA-II.

Patients with Mallampati score 1 and 2.

Exclusion Criteria

Patient refusal.

Patients undergoing emergency surgery.

Any known comorbidities.

Patients with uncontrolled diabetes mellitus, heart disease, morbid obesity, vertebral deformity.

Known allergy to drugs to be used in the study.

Previous bleeding disorder or coagulopathy.

Height <150 cm and >170 cm.

Patients suffering from renal or hepatic derangements.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the onset of sensory & motor block. <br/ ><br> <br/ ><br>To compare the duration of sensory and motor block. <br/ ><br> <br/ ><br>To compare the duration of post operative analgesia. <br/ ><br> <br/ ><br>Time to first rescue analgesia.Timepoint: Baseline, 4 weeks, 8 weeks
Secondary Outcome Measures
NameTimeMethod
To compare the change in vitals of a patient between before & after injection of the above drugs. <br/ ><br> <br/ ><br>To measure the pulse rate via ECG, SPO2 via pulse oximetry. <br/ ><br> <br/ ><br>To compare the changes in blood pressure, pulse rate, product of mean blood pressure and pulse rate. <br/ ><br> <br/ ><br>To check for any adverse effects or abnormal response to the drugs.Timepoint: Baseline, 4 weeks, 8 weeks
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