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Comparison of two different drugs given in spinal anaesthesia in patients undergoing any surgeries below umbilicus

Phase 2
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2023/07/054934
Lead Sponsor
Kempegowda 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.Patient aged between 18-60 years of either sex.

2.American Society Of Anaesthesiology , physical status 1&2

3.Patients scheduled to undergo infraumbilical surgeries requiring spinal anaesthesia.

Exclusion Criteria

1.Spine deformity

2.Coagulopathy.

3.Patient with severe hypovolemia

4.Infection at the lumbar puncture site.

5.Increased intracranial tension.

6.Neuromuscular disorders.

7. Pregnant women and lactating women

8.Patient with hypersensitivity to local anaesthetics.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess & compare the duration of sensory & motor block. <br/ ><br>Timepoint: sensory by pin prick method every 2 mins until the highest level is achieved then every 30min till block regress. Motor block by Modified Bromage Scale every 2mins till the bromage 3 is obtained then every 30 mins till motor block regress. <br/ ><br>0-no motor block <br/ ><br>1- inability to raise extended legs able to move knees & feet <br/ ><br>2-inability to raise extended legs & knees but able to move feet <br/ ><br>3-complete motor block
Secondary Outcome Measures
NameTimeMethod
To assess & compare the time for the need of first rescue analgesia.Timepoint: first 24 hours of post operative time.
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