Overview

Selective Spinal Anaesthesia With Hyperbaric Prilocain With 2%Provides Better Perioperative Hemodynamic Stability for Patients With Peripheral Vascular Disease and Cardiac Dysfunction in Lower Limb Surgery

Status:
Recruiting
Trial end date:
2024-12-01
Target enrollment:
0
Participant gender:
All
Summary
to compare the safety and efficacy of spinal anesthesia using Hyperbaric Prilocaine 2% versus Hyperbaric Bupivacaine 0.5% for patients with peripheral vascular disease and cardiac dysfunction.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Assiut University
Treatments:
Bupivacaine
Prilocaine
Criteria
Inclusion Criteria:

- Adult patients of aged >18 years old. Both sexes, males and females.

- The time of surgery does not exceed 75 min.

- Compensated cardiac dysfunction

- ASA physical status: II- IV

Exclusion Criteria:

- refusal

- Allergy to the studied drugs.

- Patients with contraindications to spinal anesthesia.

- Patients with advanced decompensated cardiac, renal, hepatic disease

- Coagulopathy or thrombocytopenia