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Intermediate Cervical Plexus Block on Stress Response - Trial NCT06064214

Access comprehensive clinical trial information for NCT06064214 through Pure Global AI's free database. This phase not specified trial is sponsored by Cairo University and is currently Not yet recruiting. The study focuses on Stress. Target enrollment is 66 participants.

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NCT06064214
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Trial Details
ClinicalTrials.gov • NCT06064214
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Intermediate Cervical Plexus Block on Stress Response
Effect of Bilateral Ultrasound-Guided Intermediate Cervical Plexus Block Combined With General Anesthesia on THE Stress Response in Patients Undergoing Anterior Cervical Spine Surgery. A Randomized Controlled Study

Study Focus

Stress

u/s guided intermediate cervical plexus block

Interventional

procedure

Sponsor & Location

Cairo University

Timeline & Enrollment

N/A

Dec 01, 2023

Dec 01, 2024

66 participants

Primary Outcome

• The serum cortisol level 24 hours postoperatively

Summary

The aim of the present study is to investigate the effect of Bilateral Ultrasound-Guided
 intermediate cervical plexus Block combined with general anesthesia on the stress and
 inflammatory response in patients undergoing anterior cervical spine surgery (ACSS)

ICD-10 Classifications

Stress, not elsewhere classified
Other reactions to severe stress
Reaction to severe stress, unspecified
Undue concern and preoccupation with stressful events
State of emotional shock and stress, unspecified

Data Source

ClinicalTrials.gov

NCT06064214

Non-Device Trial