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Comparative Correlation of U-TEG, TEG, and Routine Blood Tests

Comparative Correlation of U-TEG, TEG, and Routine Blood Tests

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600122309
Enrollment
Unknown
Registered
2026-04-11
Start date
2026-04-13
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Clinical applications include: bleeding disorders, coagulopathy, intraoperative/postoperative bleeding assessment, chronic diseases with coagulation abnormalities, acute traumatic bleeding, and orthopedic trauma.

Interventions

Gold Standard:Conventional coagulation tests (APTT and fibrinogen [FIB]) , routine blood test results, and standard thromboelastography (TEG) using kaolin cup are used as the reference standards to ev
Index test:Ultrasound guided wave thromboelastography (U-TEG) — including parameters such as R (reaction time), K (kinetics time), and MA (maximum amplitude) — is used to evaluate the coagulation stat

Sponsors

Huzhou Center Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: For adults with sodium citrate anticoagulation, the residual sample size should be >=1.5 mL. Samples from both the four routine coagulation tests and the ordinary cup (kaolin cup) of thromboelastography should be conducted simultaneously, and within 8 hours after the routine coagulation test (if this standard cannot be met for various reasons, samples within 48 hours after the completion of the test can be obtained for enrollment).

Exclusion criteria

Exclusion criteria: Residual blood samples with obvious coagulation in the tube should be excluded

Design outcomes

Primary

MeasureTime frame
U-TEG parameters, traditional thromboelastography (TEG) parameters, and conventional coagulation test results;

Countries

China

Contacts

Public ContactWang Xiaoyan

Huzhou Center Hospital

wxyjpt61@163.com+86 572 2819790

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026