UnknownNot Applicable

Intermediate Cervical Plexus Block on Stress Response

Egypt66 participantsStarted 2024-01-01

Plain-language 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)

Who can participate

Age range18 Years – 65 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 1\. ASA I \& ASA II patients.(The American Society of Anesthesiologists) 2. Age group: from 18 to 65 years old. 3. Patients undergoing anterior cervical discectomy or fixation. 4. Genders eligible for study: both sexes Exclusion Criteria: * • Patient refusal. * Patient Undergoing posterior fixation in addition to anterior. * An allergy to local anaesthetics. * Infection at block puncture site. * Bleeding disorders (Coagulopathy: PTT(partial thromboplastin time) \> 40seconds, INR(international normalised ratio) \> 1.2, platelet count \< 120 x 103 / L.). * Emergency surgeries \& patients in sepsis

What they're measuring

• The serum cortisol level 24 hours postoperatively

Timeframe: pre operative and after 24 hours of operation

Trial details

NCT IDNCT06064214

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-11-01

Contact for this trial

ahmed raafat, master's

01278996596 ahmedtaha840@hotmail.com

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