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Clinical Trials/CTRI/2023/07/054969
CTRI/2023/07/054969
Not yet recruiting
Phase 4

To evaluate the efficacy of hyperbaric bupivacaine versus hyperbaric ropivacaine in equipotent doses in unilateral spinal anaesthesia in patients undergoing infraumblical surgeries

DEPARTMENT OF ANAESTHESIA0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: S820- Fracture of patellaHealth Condition 2: S822- Fracture of shaft of tibiaHealth Condition 3: S821- Fracture of upper end of tibia

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Health Condition 1: S820- Fracture of patellaHealth Condition 2: S822- Fracture of shaft of tibiaHealth Condition 3: S821- Fracture of upper end of tibia
Sponsor
DEPARTMENT OF ANAESTHESIA
Status
Not yet recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • •HEMODYNAMICALLY STABLE
  • •BMI \-18\.5\-29\.9

Exclusion Criteria

  • •PATIENTS REFUSAL
  • •PATIENT WITH AUTONOMICAL DEFORMITIES
  • •PATIENT WITH BLEEDING DISORDER
  • •PATIENT WITH LOCAL INFECTION AT SITE OF SPINAL ANAESTHESIA
  • •PATIENTS WITH HISTORY OF CARDIOVASCULAR RENAL HEPATIC RESPIRATORY ENDOCRINE
  • •PATIENTS ON ANTICOAGULANTS
  • •DURATION OF SURGERY MORE THAN 2 HOURS

Outcomes

Primary Outcomes

Not specified

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