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Comparison of the effects of the two drugs dexmedetomidine and midazolam when given for spinal anaesthesia

Not Applicable
Conditions
Health Condition 1: null- Patients with major co-morbid conditions
Registration Number
CTRI/2018/03/012353
Lead Sponsor
Dr J Jancy
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1)Age 18-60 years.

2)American Society of Anaesthesiologists (ASA) Grade I and II.

Exclusion Criteria

1)Patient refusal for subarachnoid block

2)Known allergy to the study drugs

3)Infection at the puncture site

4)Coagulation disorders

5)Neurological disorders

6)Hepatic and renal disorders

7)Use of antipsychotic medications

8)Body mass index >= 30kg/m2

9)Pregnancy & lactation

10)ASA >= III

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Onset and duration of sensory and motor blockTimepoint: 1)Onset of motor and sensory block will be assessed every 3min for the first 15 min after spinal anaesthesia. <br/ ><br>2) Duration of motor and sensory block will be assessed at the end of surgery in the post operative period.
Secondary Outcome Measures
NameTimeMethod
Haemodynamic stability <br/ ><br>Duration of analgesiaTimepoint: During the course of surgery <br/ ><br>At the end of 24hr
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