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Comparison Low-volume Versus Standard-volume Ultrasound-guided Bilateral Intermediate Cervical Plexus Block

Name: Comparison Low-volume Versus Standard-volume Ultrasound-guided Bilateral Intermediate Cervical Plexus Block — clinical trial record (NCT07789548)
Creator: DataLookout
License: https://creativecommons.org/licenses/by/4.0/

Study acronym: ICPB

StatusRecruiting

PhasePhase 4

SponsorAssiut University

Started2026-09-01

View on ClinicalTrials.gov ↗

Amendment history

2026-08-31

Study Status, Contacts/Locations v1

Recruitment opened

Start dateestimated 2026-09-25→confirmed 2026-09-01

Study sitesdetails revised at 1 of 1 site

2026-08-24

Original filing

Assiut University

1,604 trials monitored

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Thyroidectomy is commonly associated with mild-to-moderate postoperative pain that may affect respiratory function and recovery. Bilateral intermediate cervical plexus block provides effective analgesia, but larger local anesthetic volumes may increase phrenic nerve spread and diaphragmatic dysfunction. Low-volume ultrasound-guided block may provide adequate analgesia while better preserving diaphragmatic function and postoperative respiratory performance

Trial Details

NCT Number	NCT07789548
Lead Sponsor	Assiut University
Conditions	Post Operative Pain Relief After Thyroidectomy
Enrollment	60 participants
Start Date	2026-09-01
Primary Completion	2028-09-25 (estimated)
Study Completion	2028-10-25 (estimated)
Updated on ClinicalTrials.gov	2026-09-01