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Trials / Completed

CompletedNCT06394960

Factors Predicting Blood Pressure Change With Interscalene Block

Factors Predicting Blood Pressure Change Associated With Interscalene Block, Prospective and Observational Study

Status
Completed
Phase
Study type
Observational
Enrollment
110 (actual)
Sponsor
Konya City Hospital · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Accepted

Summary

The primary aim of this study is to identify potential anthropometric features that predict the relationship between the Interscalene Block procedure and changes in blood pressure

Detailed description

This prospective, randomized study will be carried out after obtaining the necessary ethical approval and informed consent from the patients. 110 adult volunteer patients who will undergo ISB for shoulder surgery anesthesia will be included in this study. Evaluation of the patients before ISB and anthropometric measurements before and after Interscalene Block will be performed by an anesthesiologist who is not involved in the study.

Conditions

Timeline

Start date
2024-05-02
Primary completion
2024-07-10
Completion
2024-07-20
First posted
2024-05-01
Last updated
2024-07-23

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT06394960. Inclusion in this directory is not an endorsement.

Factors Predicting Blood Pressure Change With Interscalene Block (NCT06394960) · Clinical Trials Directory