Clinical Trial

The Effect of Anthropometric Measurements on Block Success, Performance Time , and Ultrasound Visibility Score.

Enrolling by Invitation
View on ClinicalTrials.gov →
Summary
The primary objective of this study is to determine whether patients' physical characteristics hold predictive value regarding the difficulty or ease of performing an interscalene block. By pre-identifying patients prone to difficult blocks, predicting procedure duration, and elucidating the factors influencing ultrasound image quality, this study aims to contribute to clinical practice and patient safety.
Trial Details
NCT Number NCT07688889
Lead Sponsor Amasya University
Conditions Interscalene Blocks
Enrollment 84 participants
Start Date 2026-06-16
Primary Completion 2027-03-01 (estimated)
Study Completion 2027-03-01 (estimated)
Updated on ClinicalTrials.gov 2026-07-07