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Hematopoietic Stem Cell-containing Autologous Blood Transfusion for Bone Marrow Protection

The aim of this project is to promote the reconstruction of haematopoietic function after chemoradiotherapy for cervical cancer with the innovative use of autologous haematopoietic containing stem cell blood transfusion support.To explore the effect of stored hemopoietic stem cell support therapy on bone marrow protect

Condition(s)Cervical Cancer
StatusRecruiting
PhaseNA
Study typeInterventional
SummaryThe aim of this project is to promote the reconstruction of haematopoietic function after chemoradiotherapy for cervical cancer with the innovative use of autologous haematopoietic containing stem cell blood transfusion support.To explore the effect of stored hemopoietic stem cell support therapy on bone marrow protection after concurrent chemoradiotherapy, in order to promote its clinical application.
Who can participateInclusion Criteria: 1)18-60 years old; 2)there are radiotherapy and chemotherapy indicators for cervical cancer;3)pathological diagnosis of squamous, adenocarcinoma or adenosquamous carcinoma;4)the Eastern Cooperative Oncology Group (ECOG) performance status score≤1; 5)the expected survival time was more than 3 months; 6)pre-menopausal women (post-menopausal women must have been postmenopausal for at least 12 months to be considered infertile), and the serum pregnancy test results are negative;7)all patients must agree to take effective contraceptive measures during the study period and within 6 months after stopping treatment;8)the subjects voluntarily participate in this clinical trial sign an informed consent form and are able to complete the study procedures and follow-up examinations.
Ages18 Years to 60 Years
SexFemale
Lead sponsorChongqing University Cancer Hospital
LocationsChongqing, Chongqing Municipality, China
Start date2022-04-13
NCT IDNCT05401175
Official listinghttps://clinicaltrials.gov/study/NCT05401175

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