About this trial
Exploring and evaluating the efficacy of herombopag in preventing thrombocytopenia due to radiotherapy for cervical cancer
Eligibility criteria
Qualifiers
Volunteer to participate in the trial and sign the informed consent
Pathologically or cytologically confirmed cervical cancer
aged 18 years or older
ECOG performance score 0-1
Disqualifiers
Participants with other diseases of hematopoietic system, including but not limited to leukemia, primary immune thrombocytopenia, myeloproliferative diseases, multiple myeloma, and myelodysplastic syndrome
Participants with thrombocytopenia occurred within the last 6 months due to causes other than CTIT, including but not limited to chronic liver disease, hypersplenism, infection
Bone marrow invasion or metastasis
History of severe cardiovascular disease within the last 6 months, such as congestive heart failure (NYHA heart function score III-IV), arrhythmias known to increase the risk of thromboembolism such as atrial fibrillation, after coronary stenting, angioplasty, and para-coronary transplantation, etc
Trial design
Treatments tested in this trial
- herombopag