MedPath

To compare Fentanyl versus Dexmedetomidine as an additional drug to hyperbaric Ropivacaine for spinal anaesthesia in below umbilical surgeries.

Phase 4
Registration Number
CTRI/2024/08/072444
Lead Sponsor
Dr Ashmeet Laller
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

AMERICAN SOCIETY OF ANESTHESIOLOGISTS(ASA) PHYSICAL STATUS CLASS 1 AND 2

Exclusion Criteria

1.Patient’s refusal .

2.Patient having Bleeding disorders .

3.Patient having Neurological disease.

4.Patient having Local skin infections at the site of spinal block.

5.Patient having Severe back deformities.

6.Patient having Raised intracranial pressure

7.Patient having Cardiac and respiratory disease

8.Patient of Morbid obesity

9.Patient having allergy to study drugs

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.Onset of sensory block: The onset of sensory block at T-10 level will be taken as the time from injection of anesthetic solution to the loss of sensation to pinprick. <br/ ><br>2.Duration of sensory block: Duration will be taken as from time of onset to time at which patient feel sensation to pinprick. <br/ ><br>3.Onset of motor block: Onset time of motor block will be taken as the time to acquire complete motor block after the intrathecal injection of local anesthetic. <br/ ><br>4.Duration of motor block: Total duration will be taken as time to completely recover from the motor block. <br/ ><br>Timepoint: Total duration will be taken as time to completely recover from the block
Secondary Outcome Measures
NameTimeMethod
•Hypotension <br/ ><br>•Bradycardia <br/ ><br>•Nausea <br/ ><br>•Vomiting <br/ ><br>•Shivering <br/ ><br>Timepoint: Total duration will be taken upto 6 hours.
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