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A Urine Sample Collection Study in Apparently Healthy Adults and Adults With Chronic, Stable Morbidities

A Urine Sample Collection Study in Apparently Healthy Adults and Adults With Chronic, Stable Morbidities

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05853016
Enrollment
600
Registered
2023-05-10
Start date
2022-03-21
Completion date
2023-05-31
Last updated
2023-05-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Disease, Healthy

Brief summary

The objective of this study is collect urine samples from healthy adult subjects and subjects with stable chronic morbidities for future testing to serve as controls and establish reference ranges in the development of new invitro diagnostic devices.

Interventions

Urine will be collected and banked for future analysis with the NEPHROCLEAR CCL14 Test

Sponsors

Astute Medical, Inc.
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Cohort A Inclusion Criteria: 1. Apparently healthy adults (age \> 21 years); 2. Provide written informed consent for study participation.

Exclusion criteria

1. Any known or suspected acute illness or condition - including acute infections - at the time of enrollment or within the previous 30 days; 2. Any known or suspected significant new onset or chronic morbid medical condition such as those listed in the inclusion criteria for Cohort B; 3. Trauma-related surgery within the last 6 months; 4. Any surgery, hospitalization or institutionalization (such as in a nursing home) during the previous 3 months; 5. Received any blood product transfusion within the previous 2 months; 6. Pregnant women or children; 7. Prisoners or institutionalized individuals; 8. Already provided a urine sample for this study. Cohort B Inclusion Criteria: 1. Adults (age \> 21 years); 2. One or more of the following chronic, stable morbid conditions: i. Active cancer ii. Arrhythmia (atrial fibrillation, heart block, ventricular tachycardia) iii. Chronic coagulation abnormality iv. Chronic obstructive pulmonary disease (including emphysema, chronic bronchitis, and asthma) v. Chronic pancreatitis vi. Chronic renal insufficiency vii. Congestive heart failure viii. Coronary artery disease ix. Diabetes mellitus (Type 1 or Type 2) x. Gout xi. Hyper- or hypothyroidism xii. Hyperlipidemia (includes hypercholesterolemia) xiii. Hypertension xiv. Immunocompromised xv. Inflammatory bowel disease (including Crohn's disease and ulcerative colitis) xvi. Liver cirrhosis xvii. Neuromuscular disease xviii. Peripheral vascular disease (a.k.a. peripheral artery disease) xix. Polycystic kidney disease xx. Rheumatoid arthritis xxi. Systemic Lupus Erythematosus c. Provide written informed consent for study participation.

Design outcomes

Primary

MeasureTime frame
Reference interval as defined by Clinical and Laboratory Standards Institute guideline EP28 for urinary C-C motif chemokine 14 concentration measured with the NEPHROCLEAR CCL14 Test within each cohortDetermined for urine sample collected at baseline

Countries

United States

Contacts

Primary ContactClinical Scientist
IA-clinical-affairs@biomerieux.com314-728-1603

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026