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NCT05762159

Analgesic Territory Assessment of the Spinal Erector Block Using Pupillometry

Centre Hospitalier Universitaire de Saint Etienne·ClinicalTrials.gov·otherRecruiting
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Study focus
Disease/Condition
Anesthesia, Local
Drug/Device/Intervention
data collected
Study type
Observational
Intervention type
other
Sponsor & location
Primary sponsor
Centre Hospitalier Universitaire de Saint Etienne
Location
Saint-Étienne, France
Timeline & enrollment
Phase
N/A
Start date
Mar 10, 2023
End date
Nov 01, 2023
Enrollment
40 participants
Primary outcome

variation of the pupil size (in percentage)

Summary

Few works have studied the area of analgesia covered by the spinal erector block in an
 objective manner, especially on the cephalo-caudal spread. The available data are dissection
 works or subjective data such as thermoalgesic or epicritic sensitivity.
 
 This information would however be relevant in order to propose a better analgesia. Indeed, it
 could explain certain failures by insufficient diffusion of the block. The use of a
 multistage block could be relevant, especially in the case of osteosynthesis on several
 vertebral levels.

ICD-10 classifications
Local anaestheticsAnaesthetic, unspecifiedOther and unspecified general anaestheticsPoisoning: Local anaestheticsParenteral anaesthetics
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT05762159
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT05762159 through Pure Global AI's free database. This phase not specified trial is sponsored by Centre Hospitalier Universitaire de Saint Etienne and is currently Recruiting. The study focuses on Anesthesia, Local. Target enrollment is 40 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.