Viewing Study NCT06600048



Ignite Creation Date: 2024-10-26 @ 3:40 PM
Last Modification Date: 2024-10-26 @ 3:40 PM
Study NCT ID: NCT06600048
Status: RECRUITING
Last Update Posted: None
First Post: 2024-09-12

Brief Title: Spinal Anesthesia by Hyperbaric Prilocaine in Day-Case Perianal Surgery
Sponsor: None
Organization: None

Study Overview

Official Title: Spinal Anesthesia by Hyperbaric Prilocaine in Day-Case Perianal Surgery A Randomized Controlled Trial
Status: RECRUITING
Status Verified Date: 2024-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The aim of this study is to evaluate the effect of spinal anesthesia by hyperbaric prilocaine in day-case perianal surgery
Detailed Description: Day-case spinal anesthesia with short-acting local anesthetics such as lidocaine and chloroprocaine can provide short times to discharge However the association of lidocaine with transient neurologic symptoms TNS and chloroprocaine with neurologic injury has limited the use of these agents in spinal anesthesia

Hyperbaric bupivacaine has been used for spinal anesthesia for decades owing to the low incidence of TNS

Prilocaine is also an amide local anesthetic that has an intermediate duration of action It is available in the hyperbaric form that can be used for spinal anesthesia in day-case surgeries

Hyperbaric prilocaine provides faster spinal block onset and earlier patient recovery in ambulatory surgery compared to plain prilocaine

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None