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An Observational Study of Recombinant Human Thrombopoietin (rhTPO) in the Treatment of Infection-Associated Thrombocytopenia

A Prospective, Single-Center, Real-World Clinical Study of Recombinant Human Thrombopoietin (rhTPO) in the Treatment of Infection-Associated Thrombocytopenia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600128498
Enrollment
Unknown
Registered
2026-07-21
Start date
2026-08-30
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Infection-associated thrombocytopenia

Interventions

recombinant human thrombopoietin (rhTPO):None
historical control group(Conventional treatment):None

Sponsors

Shandong Provincial Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. (1) PLT = 30 x 10^9/L from the platelet count measured 48 hours earlier. 3. The patient or their legal guardian has signed the informed consent form, demonstrates good compliance, and is willing to cooperate with follow-up visits.

Exclusion criteria

Exclusion criteria: 1.Known history of allergy to rhTPO. 2.History of thrombosis or bleeding disorders. 3.Pregnancy or breastfeeding, or inability to take effective contraceptive measures during the study period. 4.Participation in another clinical study involving platelet-elevating agents within 14 days prior to screening. 5.Contraindication to any required concomitant medication or supportive therapy. 6.Concurrent severe hematological diseases (e.g., aplastic anemia, myelodysplastic syndrome, leukemia, etc.). 7.End-stage hepatic or renal failure, hematopoietic system disorders, or malignant tumors. 8.Thrombocytopenia caused by other factors, such as chemotherapy/radiotherapy-related thrombocytopenia, massive hemorrhage, or immune thrombocytopenia (ITP). 9.Any active severe psychiatric disorder, medical condition, or other situation that, in the investigator‘s judgment, may affect treatment adherence, compliance, or the ability to provide informed consent.

Design outcomes

Primary

MeasureTime frame
The time required for platelet count to recover to = 100 × 10^9/L;

Secondary

MeasureTime frame
incidence rate of adverse events;30?day survival rate after discharge;improvement in bleeding events;Day 7 Platelet Relative Change Rate;Platelet transfusion rate (frequency and quantity);Total efficiency (CR + R);

Countries

China

Contacts

Public ContactSun Liang

Shandong Provincial Third Hospital

sun_linquan@163.com+86 531 8165 6639

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026