Clinical trial · Interventional
rhTPO Mobilized Auto Cryo Platelets For GYN Patients Receiving Carboplatin
A Pilot Study of Transfusion of rhTPO-Derived Autologous Platelets Cryopreserved With Thrombosol and 2% DMSO in Patients With Gynecologic Malignancy Receiving Carboplatin
NCT00038012CI-TRIAL-00035577completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
A Pilot Study of Transfusion of rhTPO-Derived Autologous Platelets Cryopreserved with ThromboSol and 2% DMSO in Patients with Gynecologic Malignancy Receiving Carboplatin
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Neoplasms, Gynecologic | Female Reproductive System Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Carboplatin | Drug | Carboplatin | ALIAS |
| Platelet-pheresis | Procedure | — | UNRESOLVED |
| Thrombopoietin | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- rhTPO-Derived Autologous Platelets Transfusion
- interventionNames
- Drug: Thrombopoietin
- Procedure: Platelet-pheresis
- Drug: Carboplatin
Primary outcomes (1)
- measure
- Response Rate
- timeFrame
- Continuous
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 15 Years
Show eligibility criteria text
INCLUSION CRITERIA: * Patients with gynecologic malignancy for whom treatment with carboplatin is indicated. * Age \>/= 15 years. * Adequate hematologic, renal, and hepatic functions. * Life expectancy \>/- 3 months. Karnofsky Performance Status \>/= 80. * Signed informed consent form. EXCLUSION CRITERIA: * Patients with rapidly progressive disease. * Pregnant or lactating women. * Patients with comorbid condition which renders patients at high risk of treatment complication. * History of CNS metastasis. * Patients with significant cardiac disease (NYHA Class III or IV), dysrhythmia, or recent history of MI or ischemia, transient ischemic attack or CVA within the 6 months of study entry. * Prior chemotherapy, immunotherapy, any experimental drug within 4 weeks, use of myeloid (G-CSF or GM-CSF) growth factors within 2 weeks or erythropoietin within 4 weeks. * Use of any nitrosourea (BCNU, CCNU) or mitomycin - C within 6 weeks. * Prior surgery or RT within 2 wks of study entry. * Patients with history of prior high dose chemotherapy with stem cell transplant or with history of prolonged thrombocytopenia (\> 2 weeks). * History of leukemia. * History of any platelet disorders including ITP, TTP or bleeding disorders. * History of \> 3 prior chemotherapy regimens (all platinum regimens will be counted as 1 regimen). * Demonstrated lack of response to platinum-based therapy.
References
Publications (0)
Data not yet available
No reference posted for this study.