Clinical trial · Observational
Multi-modal Quantitative Imaging of the Skin
DermaFlow Alpha - Multi-modal Quantitative Imaging of the Skin
NCT06989216CI-TRIAL-00090166DermaFlowrecruitingClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This clinical trial is about evaluating the suitability of multi-modal imaging technology, which covers virtually the entire body, to evaluate the possibility of screening and early detection of disease.
Conditions
Conditions (7)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Atopic Dermatitis | — | UNRESOLVED | — |
| Diabetic Foot | — | UNRESOLVED | — |
| Peripheral Arterial Disease | — | UNRESOLVED | — |
| Psoriasis | — | UNRESOLVED | — |
| Raynaud Disease | — | UNRESOLVED | — |
| Skin Cancer | Malignant Skin Neoplasm | ALIAS | 0.90 |
| Skin Diseases | — | UNRESOLVED | — |
Interventions
Interventions (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (1)
- label
- patient_cohort
- description
- The study participants mainly consist of a prospective primary care population. All patients visiting the clinical sites, seeking care, or as separately invited, are offered to participate in this investigation. This includes sub-groups of patients with skin cancer and dermatological conditions.
Primary outcomes (5)
- measure
- Sensitivity for detection of lesions requiring excision in comparison to visual inspection
- timeFrame
- Typically same day as enrolment, or if follow-up then 1 year following enrolment.
- description
- Evaluate the sensitivity of detecting lesions that required excision by inspection and labelling of full-body color images acquired by full-body photography. Manual labelling of images acquired by full-body photography will be compared to ocular inspection by doctor on-site, performed as part of a standard primary care flow. An expert reviewer blinded to outcome from ocular inspection will perform the manual labelling of images.
- measure
- Difference in body metrics between full-body 3D photography and traditional measurements
- timeFrame
- Typically same day as enrolment, or if follow-up then 1 year following enrolment.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion criteria: * Adult patients that are part of the regular healthcare patient flow at the investigational sites, or as separately invited to participate in this investigation. * Patients with signed informed consent Exclusion criteria: * Cognitive impairment * Patients unable to understand the oral and written study information in Swedish or English * Other severe disorder or terminal disease * Patients unable to provide an informed consent * Patients not able to keep balance, while standing up with closed eyes, without any aid * Claustrophobic patients
References
Publications (0)
Data not yet available
No reference posted for this study.