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Clinical Trials/CTRI/2018/05/014273
CTRI/2018/05/014273
Recruiting
Phase 2

Comparative evaluation of two different doses of dexmedetomidine as an adjunct to levobupivacaine for subarachnoid block for lower abdominal surgeries

Srishti Verma0 sites0 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Not specified
Sponsor
Srishti Verma
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Srishti Verma

Eligibility Criteria

Inclusion Criteria

  • ASA grade I and gradeII patients
  • patients with weight from 45kgs to 85kgs
  • patients with height not less than 150 cms
  • Patients undergoing lower abdominal surgeries

Exclusion Criteria

  • Patients refusal to be a part of the study
  • Previous spinal surgeries( technically difficult subarachnoid block)
  • Spine deformities
  • Local site infection and coagulation abnormalities, allergy to local anaesthetics or study medications
  • neuromuscular diseases
  • patients with hematological , neurological and psychiatric diseases
  • patients with heart block ,dysrrthymias and labile hypertension

Outcomes

Primary Outcomes

Not specified

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