Last updated: January 21, 2024
Sponsor: Cairo University
Overall Status: Active - Recruiting
Phase
N/A
Condition
Stress
Treatment
u/s guided intermediate cervical plexus block
Clinical Study ID
NCT06064214
cervical plexus block
Ages 18-65 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- 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 orfixation. 4. Genders eligible for study: both sexes
Exclusion
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
Study Design
Total Participants: 66
Treatment Group(s): 1
Primary Treatment: u/s guided intermediate cervical plexus block
Phase:
Study Start date:
January 01, 2024
Estimated Completion Date:
December 01, 2024
Study Description
Connect with a study center
Ahmed Raafat
Giza, October 002
EgyptActive - Recruiting
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