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Clinical Trial of Creatinine Test Strips (Dry Electrochemical Method)

Clinical Trial of Creatinine Test Strips (Dry Electrochemical Method)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400093552
Enrollment
Unknown
Registered
2024-12-06
Start date
2023-10-10
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

nephrosis

Interventions

Gold Standard:Abbott Point of Care Inc.,i-STAT CHEM8+ Cartridge, i-STAT 1 Handheld Blood Meter, Model: 300-G
Index test:Creatinine Test Strips (Dry Electrochemical Method), Model: iCR10
Handheld Electrochemical Meter, Model: M432

Sponsors

Nanjing Hospital of C.M.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged 18 and above, gender unrestricted, with stable vital signs. 2. Hematocrit (HCT) between 30% and 60% inclusive. 3. Voluntarily participate in this clinical trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Individuals with severe mental disorders or other conditions that prevent them from cooperating. 2. Those who are illiterate. 3. Subjects with incomplete information (including but not limited to gender, age, clinical diagnosis, etc.). 4. Other situations deemed unsuitable for participation in this clinical trial by the investigator.

Design outcomes

Primary

MeasureTime frame
Outlier;correlation ;bias;—

Countries

China

Contacts

Public ContactWei Kong

Nanjing Hospital of C.M.

KW-9009@163.com+86 189 5175 5181

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026