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Clinical Trials in the Netherlands / NCT05912153
Recruiting Observational

SPECT-CT vs MRI for the Diagnosis of Osteoarthritis in the Foot and Ankle

NCT05912153 · tracked via the Priya Life Science Netherlands tracker
Phase
Observational
Started
2023-07-04
Last updated
2026-02-27

Condition(s) studied

Osteoarthritis AnkleOsteoarthritis

Investigational drug(s) / intervention(s)

SPECT/CTMRI

SPECT/CT: SPECT/CT of the foot and ankle

MRI: MRI of the foot and ankle

Study summary

The diagnose of symptomatic osteoarthritis in the ankle, mid- and hind foot remains challenging. There is no gold standard for the work-up and various hospitals use different protocols. Current literature shows a promising role for SPECT-CT imaging in ankle, hind- and midfoot OA. In a previous study investigating the role of SPECT-CT in a reproducible group we have observed a change in diagnosis in 53% when SPECT-CT data was added to the data of conventional workup alone. In 26% of patients addition of SPECT-CT data resulted in change of the original treatment plan. To our knowledge no prospective studies are available on this subject for both SPECT-CT and MRI. In our clinic both SPECT-CT and MRI are used in the work-up for patients with ankle, hind- and midfoot pain. Although we experience good result with SPECT-CT, MRI might be able to detect symptomatic OA as well. Moreover MRI provide more information about soft tissue and is less harmful for the patient in comparison to SPECT-CT. The aim of this study is to determine the diagnostic performance of SPECT-CT and MRI when used routinely in patients with symptomatic OA of the ankle, hind- and midfoot.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Suspected symptomatic ankle, hind- or midfoot OA * Informed consent * Age ≥ 18 years * Average NRS ≥4 over the past week. Exclusion Criteria: * Contraindication for surgery * Contraindication for SPECT-CT or MRI * Contraindication for intra-articular injections * Isolated forefoot pathology * Fracture, ligamentous or tendon injury of the ankle, hind- and/or midfoot trauma within one year before presentation * History of neurological disease * History of foot and/or ankle surgery (affected side) * Inability to read and understand the written information

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Martini Hospital Groningen Netherlands Recruiting

More Martini Hospital Groningen trials in the Netherlands

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05912153 on ClinicalTrials.gov ↗ ← All trials in the Netherlands