Clinical trial · Observational
Bone Marrow Imaging and Clinical Outcomes Across Hematologic, Oncologic, and Other Relevant Conditions
NCT07743476CI-TRIAL-00126422recruitingClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 19, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260919-000001
Summary
Brief summary (as posted)
An observational study of patients with hematologic, oncologic, and other relevant conditions undergoing bone marrow imaging, with longitudinal collection of imaging, treatment, and clinical outcome data to characterize bone marrow features and changes over time
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Bone Marrow | — | UNRESOLVED | — |
| Hematologic | — | UNRESOLVED | — |
| Oncologic | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Data Collection | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- Bone marrow imaging characteristics.
- timeFrame
- Through study completion; an average of 1 year.
- description
- Evaluation of bone marrow imaging findings and longitudinal changes in patients with hematologic, oncologic, and other relevant conditions.
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
Inclusion Criteria * Diagnosis of a hematologic, oncologic, or other condition relevant to the study. * Availability of clinical, imaging, laboratory, treatment, and/or outcome data relevant to the study. * Ability to provide informed consent for prospective participation or, for pediatric participants, parent/legal guardian permission with assent when applicable. * Participants undergoing research MRI must be eligible for MRI according to institutional safety requirements. Exclusion Criteria * Inability to provide required informed consent or parental/legal guardian permission for prospective participation. * Insufficient clinical information to support study participation * Pregnancy. * Contraindication to MRI will exclude participants from research-specific MRI but not necessarily from other study components.
References
Publications (0)
Data not yet available
No reference posted for this study.