New shoulder dye could sharpen MRI images
NCT ID NCT07057037
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new injection called NEMO-103 to see if it makes shoulder MRI pictures clearer for diagnosing problems like torn tendons or cartilage. About 85 adults with known or suspected shoulder issues will get both a regular MRI and one with the injection. The goal is to see if the dye improves image quality to help doctors make better diagnoses.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 85 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2025
- Expected to finish
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Aug 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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19 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age ≥19 years at the time of informed consent. 2. Suspected or known shoulder joint diseases requiring MRA for diagnosis or evaluation at screening. 3. Voluntarily decided to participate in the study and provided written consent after receiving a sufficient explanation about this study and after fully understanding the information. Exclusion Criteria: 1. Subjects with contraindications to MRI 2. Subjects expected to be clinically unstable during the study 3. Subjects who have received or used another IP or investigational device within 4 weeks or ≥5 half-lives, whichever is longer, prior to informed consent. 4. Pregnant or breast-feeding women, or women of childbearing potential and men who do not agree to use appropriate methods of contraception during the study. 5. Determined to be ineligible to participate in the study by the investigator due to any other reasons.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Asan Medical Center
Seoul, Seoul Teugbyeolsi, 5505, South Korea
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Gangnam Severance Hospital
Seoul, Seoul Teugbyeolsi, 06273, South Korea
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Konkuk University Medical Center
Seoul, Seoul Teugbyeolsi, 05030, South Korea
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Korea University Guro Hospital
Seoul, Seoul Teugbyeolsi, 08308, South Korea
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Seoul National University Bundang Hospital
Seongnam-si, Gyeonggi-do, 13620, South Korea
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Seoul National University Hospital
Seoul, Seoul Teugbyeolsi, 0308, South Korea
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The Catholic University of Korea Seoul ST. Mary's Hospital
Seoul, Seoul Teugbyeolsi, 06591, South Korea
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Yonsei University Health System, Severance Hospital
Seoul, Seoul Teugbyeolsi, 03722, South Korea
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Muscle chain therapy put to the test for frozen shoulder
- Can a Stomach-Derived peptide help tendons heal faster after surgery?
- Can a patch make torn shoulder tendons heal stronger?
- Blood-derived injections may mend torn shoulder tendons without surgery
- Can radiofrequency waves unfreeze a stiff shoulder?
- Ultrasound 'Tissue Stiffness' test could reveal hidden rotator cuff healing problems