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NCT06803056 · ClinicalTrials.gov registry record · NA
QUANTIFY: Quantitative Understanding of Advanced Novel Techniques for Imaging Fasciitis and Yielding Biomarkers
A NA study of Achilles Tendinopathy and Plantar Fasciopathy, sponsored by Ruth Chimenti.
- Recruiting
- Registry status
- NA
- Development phase
- 120
- Enrollment target
- 1
- Study location
NCT06803056 is a NA study of Achilles Tendinopathy and Plantar Fasciopathy that is actively recruiting participants, run by Ruth Chimenti. The registered enrollment target is 120 participants, above the 103-participant average among 3 other Achilles Tendinopathy trials with a reported enrollment target (17% higher). The trial reports 1 study location across 1 state.
The verdict
NCT06803056, a NA study of Achilles Tendinopathy and Plantar Fasciopathy, is actively recruiting participants, sponsored by Ruth Chimenti.
- RECRUITING
- Registry status
- NA
- Development phase
- 120 participants
- Enrollment target
- 1
- Study location
Study Summary
This study is to create a test that can accurately find and measure the problem areas in muscle and fascia tissue, also known as myofascial pain. The hypothesis is that a combination of imaging findings will be able to detect when myofascial pain is present. The goal is to improve management of myofascial pain by making better tools to find changes in the muscle and fascia tissues for a more personalized treatment. This project was funded by the HEAL initiative (https://heal.nih.gov/).
Conditions Studied
Interventions
- DIAGNOSTIC_TEST Ultrasound imaging
- DIAGNOSTIC_TEST Magnetic Resonance Imaging
- DIAGNOSTIC_TEST Clinical exam
Study Locations (1)
Iowa
- University of Iowa Health Care - Iowa City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Start Date | 2025-05-22 |
| Est. Completion | 2026-08 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06803056
The ClinicalTrials.gov registry entry for NCT06803056 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 103-participant average among 3 other Achilles Tendinopathy trials with a reported enrollment target (17% higher). The listed sponsor is Ruth Chimenti, which has 4 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Achilles Tendinopathy appearing as the primary indexed condition, and to 3 interventions - of which Ultrasound imaging is the first listed.
NCT06803056 reports 1 study location spanning 1 distinct geographic area - top geographies include Iowa.
Frequently Asked Questions
What is clinical trial NCT06803056 about?
NCT06803056 is a clinical study titled "QUANTIFY: Quantitative Understanding of Advanced Novel Techniques for Imaging Fasciitis and Yielding Biomarkers". This study is to create a test that can accurately find and measure the problem areas in muscle and fascia tissue, also known as myofascial pain. The hypothesis is that a combination of imaging findings will be able to detect when myofascial pain is present. The goal is to improve management of myof...
What is the current status of trial NCT06803056?
This trial is currently recruiting. It is a NA study. The enrollment target is 120 participants. The study started on 2025-05-22. Estimated completion is 2026-08.
What conditions does trial NCT06803056 study?
This clinical trial studies the following conditions: Achilles Tendinopathy, Plantar Fasciopathy, Controls.
What interventions are being tested in trial NCT06803056?
The interventions under investigation include: Ultrasound imaging (DIAGNOSTIC_TEST), Magnetic Resonance Imaging (DIAGNOSTIC_TEST), Clinical exam (DIAGNOSTIC_TEST).
Who is sponsoring clinical trial NCT06803056?
This trial is sponsored by Ruth Chimenti, which has 4 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06803056 being conducted?
This trial has 1 study location across Iowa. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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