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Presence of the Arcade of Struthers on Preoperative Ultrasound

N/A

Waitlist Available

Led By Tuna Ozyurekoglu, MD

Research Sponsored by Christine M. Kleinert Institute for Hand and Microsurgery

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Be older than 18 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up through study completion, average of 1 day/visit

Awards & highlights

No Placebo-Only Group

Summary

To determine the correlation between the presence of the arcade of Struthers on preoperative ultrasound and during endoscopic surgery for cubital tunnel syndrome, and to determine the reliability of a portable ultrasound probe to detect the arcade of Struthers in the arm.

Eligible Conditions

Cubital Tunnel Syndrome

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ through study completion, average of 1 day/visit

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~through study completion, average of 1 day/visit

This trial's timeline: 3 weeks for screening, Varies for treatment, and through study completion, average of 1 day/visit for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.

Primary study objectives

Presence of the arcade of Struthers

Awards & Highlights

No Placebo-Only Group

All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups

Experimental Treatment

Group I: ParticipantsExperimental Treatment1 Intervention

Patients diagnosed with cubital tunnel syndrome who are being scheduled for a primary endoscopic cubital tunnel release by the principle investigator will be recruited

Treatment

First Studied

Drug Approval Stage

How many patients have taken this drug

Ultrasound

2013

Completed Phase 1

~4090

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