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

NCT07688889 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 84

Last updated 2026-07-07

No results posted yet for this study

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.

Conditions

  • Interscalene Blocks

Sponsors & Collaborators

  • Amasya University

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-06-16
Primary Completion
2027-03-01
Completion
2027-03-01

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07688889 on ClinicalTrials.gov