The Comparison of Semiconductor Embedded Therapeutic Arm Sleeves for the Treatment of ECRB Tendinopathy
Stopped early · Not applicable · Has a placebo group
Conditions studied: ECRB Tendinopathy
In brief
This study seeks to identify patient reported and clinically measured outcomes for pain management and elbow function with application of semiconductor embedded fabric combined with PRP+ASC injections in the affected area.
Key facts
- Study ID
- NCT06846593
- Run by
- INCREDIWEAR HOLDINGS, INC.
- People needed
- 5
- Starts
- 2024-11-01
- Expected to finish
- 2026-05-20
- Last updated by the study team
- 2026-05-22
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients diagnosed with ECRB tendinopathy as determined by radiographic assessment or ultrasound imaging.
- Patients age 18-65
- Patients who are willing and able to adhere to follow-up schedule and protocol guidelines.
- Patients who are willing and able to sign corresponding research subject consent form.
You may not qualify if…
- Patient has a history of neurological conditions, including multiple sclerosis or Parkinson's disease
- Patient has severe medical condition, including recent myocardial infarction, unstable angina, heart failure, severe anemia
- Patient has had prior surgical treatment of the elbow in the last 5 years or injection treatment(s) in the last 2 years
- Patient has complete tear of ECRB tendon or other surgical indication
- Patient has chronic pain conditions unrelated to elbow condition
- Patient has auto-immune or auto-inflammatory diseases
- Patient has used tobacco within the last 90 days
- Patient is not within the ages of 18-65
- Patient has a history of metabolic disorders
- Patient has an active infection (local or systemic)
- Patient is unwilling or unable to sign the corresponding research subject consent form
- Patient meets any other criteria or has any other condition that, in the opinion of the investigator, would prevent them from completing the study or that, in the opinion of the investigator, would confound study results.
Where it is running
- Bluetail Medical Group — Chesterfield, Missouri, United States
Full record on ClinicalTrials.gov
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