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Clinical Trials/CTRI/2024/05/067077
CTRI/2024/05/067077
Not yet recruiting
Phase 4

Clinical Efficacy of Hyperbaric Ropivacaine 0.75% Alone or with Fentanyl in Spinal Anaesthesia for Abdominal Hysterectomy; a Prospective Randomised Double Blind Study - NI

I0 sites0 target enrollmentTBD
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Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
I
Status
Not yet recruiting
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
I

Eligibility Criteria

Inclusion Criteria

  • •Patients with American Society of Anesthesiologists physical status I\-II, Scheduled for elective abdominal hysterectomy under Spinal Anaesthesia, Height \= 140cm, Weight: 40kg \- 65kg

Exclusion Criteria

  • •Patient refusal, Patient with Coagulopathies or on anticoagulant medication, any specific disease with absolute contraindications of Spinal Anaesthesia, hypothyroidism or diabetic neuropathy and Psychiatric disorder / disease and history of allergic reaction to study drugs.

Outcomes

Primary Outcomes

Not specified

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