Skip to content

A multicenter, randomized, controlled clinical study of TPO receptor agonist versus blank control for secondary preprevention of thrombocytopenia after lymphatic tumor chemotherapy

A multicenter, randomized, controlled clinical study of TPO receptor agonist versus blank control for secondary preprevention of thrombocytopenia after lymphatic tumor chemotherapy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059807
Enrollment
Unknown
Registered
2022-05-11
Start date
2022-05-14
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Thrombocytopenia after chemotherapy for lymphoma

Interventions

Haitripopa group:Haitripopa
Blank control group:None

Sponsors

Cancer Hospital Affiliated to Chongqing University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with various types of lymphoma clearly diagnosed by bone marrow puncture or pathological examination; 2. No chemotherapy contraindications were found, and the duration of chemotherapy was > 2 cycles; 3. The patients had a minimum platelet value =50*10^9/L but =2 points; Has received or is currently receiving radiation therapy, especially for long bones and flat bones (e.g. pelvis, sternum, etc.).; 4. Informed consent signed by the person or guardian.

Exclusion criteria

Exclusion criteria: 1. Chemotherapy contraindications exist; 2. Complicated with other malignant tumors; 3. Diseases of the immune system; 4. Severe cardiohepatic and renal impairment.

Design outcomes

Primary

MeasureTime frame
CIT level occurred again;CIT duration;

Secondary

MeasureTime frame
The total amount of platelet transfused;Side effects;Relationship between the oral time of hetripopal and the occurrence of lymphoma CIT;

Countries

China

Contacts

Public ContactXiao Chunyan

Cancer Hospital Affiliated to Chongqing University

xcy910114@163.com+86 189 8300 3257

Outcome results

None listed

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