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Active (not recruiting) Phase 4 NCT07539935

Analgesic Effect of Superficial Cervical Plexus Block in Postoperative Neck Surgeries

Phase 4 – monitoring after market approval
Conditions: Postoperative Pain

Sponsor: Sohag University

trial.available_in: БГ
Overview
analgesic effect of superficial cervical plexus block by using ultrasound in patients undergoing neck surgeries
Description
The efficacy of ultrasound-guided bilateral superficial cervical plexus block on postoperative pain relief in patients undergoing neck surgeries, prospective randomized controlled study,To assess the analgesic efficacy of bilateral superficial cervical plexus block in reducing post-operative pain following neck surgery, decrease total opoid consumption during first 24h post operative.
Who can participate
Inclusion Criteria: * The study include all patients between 18 and 60 years of age who underwent elective neck surgery under general anesthesia Exclusion Criteria: * 1\. Patient refusal . 2. Patient with significant neurological , psychological disease . 3. patient known allergy to local anesthesia . 4. Patient uncorrected coagulapathy or anticoagulant therapy . 5. Patient with sever neck deformity . 6. Patient with infection at site of injection . 7. Patient with sever respiratory disease . 8. patients with regular use of analgesic medications
Interventions
superficial cervical plexus block guided by ultrasound with bupivacaine
PROCEDURE
Paracetamol (500 mg) tablets
DRUG
Locations 1
Egypt (1)
Faculty of medicine, Sohag University.
Sohag
Technical details
Status
Active (not recruiting)
Phase
Phase 4
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Maximum age
60 Years
Healthy volunteers
No
Start date
16.03.2026
Completion date
30.10.2027
Registry ID
NCT07539935
Source
clinicaltrials.gov
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