Clinical trial · Observational
Development Study of Check-Cap Imaging System in Healthy Volunteers
NCT03989180CI-TRIAL-00056583completedClinicalTrials.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)
To evaluate the performance of Check-Cap Imaging System in healthy volunteers in a variety of operating scenarios. The Back recorder unit is the primary module for evaluation The participants DO NOT ingest a capsule and the capsules do not have any radioactive source
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Colo-rectal Cancer | Colon Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| C-Scan System | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- Performance of the C-Scan system in terms of communication between the C-Scan Capsule and the System Track in different locations, positions and configurations.
- timeFrame
- 36 months
- description
- The C-Scan System performance will be tested in different versions, configurations and locations. The C-Scan Cap with no radioactive source will be placed on the subject's abdomen and the C-Scan Track will be placed on the subject's back in different locations. The subject will be ask to continue his/her rutine daily activities such as: sleeping, driving a car, watching TV etc for a few days.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 20 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: * Male or female between 20 and 75 years of age * Subjects who are generally healthy * Subjects who fit the following body dimensions: * Height: 150-200 cm * Weight : 50-140 Kg * BMI: 20-35 * Subjects who are ready to follow the various physical activities such as: walking, running, sitting, driving, bending etc. * Subjects who are free to spend up to 4 days carrying the back recorder system. * Sign informed consent Form. Exclusion Criteria: * Subjects with cancer or other life threatening diseases or conditions * Pregnant women * Subjects with cardiac pacemaker or any other implanted or external portable medical device (i.e. infusion pumps) * Bed-ridden or sedentary subjects * Subjects who suffer significant movement limitations (who cannot follow the typical activities of walking, driving, bending, sitting etc.) * Morbid Obesity (BMI \> 35) * Subjects under custodial care * Participation in current clinical study or clinical study within 30 days prior to the procedure
References
Publications (0)
Data not yet available
No reference posted for this study.