Chloroprocaine for Inguinal Herniorrhaphy

Status Completed

Clinical Trial Summary

This study is to determine the minimum effective dose for intrathecal chloroprocaine in inguinal herniorrhaphy in outpatients using a Combined Spinal Epidural (CSE) anesthesia.

Clinical Trial Description

A standard CSE procedure will be conducted in which the patient is placed in an upright sitting position on the side of the operation table and a epidural Tuohy needle 18G will be inserted into L3-L4 interspace via a loss-of-resistance technique. The dura will be punctured using a 27-gauge pencil-point spinal needle and a certain dose of chloroprocaine 1% will be given. After the spinal needle is withdrawn, an epidural catheter will be placed and the epidural needle will be withdrawn. After fixation of catheter the patient will be placed in a supine position.

The first spinal dose of chloroprocaine 1% to start with is 50mg. This dose has been successfully used for spinal anesthesia in hernia repair outpatients to reach an adequate analgesia. Each time there will be added 2,5 microgram of sufentanil for prolongation of the analgesia. The testing interval is 2 mg. ;

Study Design

Related Conditions & MeSH terms

Spinal Anesthesia

Clinical Trial Details

NCT number	NCT03805503
Study type	Interventional
Source	University Hospital, Ghent
Contact
Status	Completed
Phase	Phase 4
Start date	September 16, 2015
Completion date	December 4, 2018

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