Comparison Low-volume Versus Standard-volume Ultrasound-guided Bilateral Intermediate Cervical Plexus Block
- NCT ID
- NCT07789548
- Registry status
- Recruiting
- Study type
- Interventional
- Phase
- Phase 4
- Sponsor
- Assiut University
- Conditions
- Post Operative Pain Relief After Thyroidectomy
Overview
ClinicalTrials.gov lists this study as Recruiting.
Official title: Comparison Between Low-volume Versus Standard-volume Ultrasound-guided Bilateral Intermediate Cervical Plexus Block for Patients Undergoing Thyroidectomy: A Randomized Controlled Trial.
Enrollment: 60 participants (Estimated).
What is being studied
- Drug: Bupivacain only
Who may be eligible
- Ages
- 18 Years to 65 Years
- Sex
- All
- Healthy volunteers accepted
- No
ClinicalTrials.gov lists the following eligibility criteria.
Study locations
1 study location is listed.
Recruiting site status is explicitly provided for 1 location; 1 is listed as Recruiting.
Countries: Egypt
Sample of listed locations
- Assiut main university hospital — Asyut, Egypt — Recruiting
Study details
- Start date
- September 1, 2026
- Primary completion date
- September 25, 2028
- Completion date
- October 25, 2028
- First posted
- August 27, 2026
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT07789548
- Registry last updated
- September 1, 2026
- QualifiedStudies registry data refreshed
- October 5, 2026
- QualifiedStudies record fetched
- October 5, 2026
View NCT07789548 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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