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Clinical Trials/CTRI/2024/02/062503
CTRI/2024/02/062503
Not yet recruiting
Phase 2

Assessment Of Ambulatory Profile Following Spinal Anaesthesia With Equipotent doses Of 0.5% Bupivacaine Versus 0.75% Ropivacaine In Perineal Surgeries- A Comparative Study - nil

Kadhij FathimaM0 sites0 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Health Condition 1: K602- Anal fissure, unspecifiedHealth Condition 2: O- Medical and SurgicalHealth Condition 3: O- Medical and Surgical
Sponsor
Kadhij FathimaM
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Kadhij FathimaM

Eligibility Criteria

Inclusion Criteria

  • 1\. All ASA I, II and III patients planned for Perineal Surgeries under Spinal Anaesthesia
  • 2\. Duration of surgery less than 2 hours

Exclusion Criteria

  • 1\. Patient refusal
  • 2\. Patients who are categorized above ASA III
  • 3\. Patients with Spine deformities
  • 4\. Patients with known allergies to Local Anaesthetics and Fentanyl
  • 5\. Patients with known neurological, psychiatric and vestibular disease

Outcomes

Primary Outcomes

Not specified

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