UnknownNot applicableNCT02779569
A Clinical Trial Evaluating the Efficacy of Ultra Low Dose of Decitabine in Myelodysplastic Syndromes (MDS)
Studying Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- The First Affiliated Hospital with Nanjing Medical University
- Principal Investigator
- Guangsheng HeThe First Affiliated Hospital with Nanjing Medical University
- Intervention
- decitabine(drug)
- Enrollment
- 80 enrolled
- Eligibility
- 18-80 years · All sexes
- Timeline
- 2016 – 2019
Study locations (6)
- No.303 Hospital of Chinese People's Liberation Army, Nanning, Guangxi, China
- Jiangsu Province Hospital, Nanjing, Jiangsu, China
- Shengjing Hospital of China Medical Univercity, Shenyang, Liaoning, China
- The First Affiliated Hospital of Xi'an Jiaotong University, Xi’an, Shanxi, China
- People's Hospital of Xinjiang Uygur Autonomous Region, Ürümqi, Xinjiang, China
- Zhejiang Provincial Hospital of TCM, Hangzhou, Zhejiang, China
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT02779569 on ClinicalTrials.govOther trials for Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent
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