Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
1000 participants
OBSERVATIONAL
2025-12-18
2029-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Shanghai Lymphoma Clinical Cohort
Shanghai Lymphoma Clinical Cohort
No interventions need to be specified for this study
No interventions need to be specified for this study
Interventions
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No interventions need to be specified for this study
No interventions need to be specified for this study
Eligibility Criteria
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Inclusion Criteria
2. Patients newly diagnosed with non-Hodgkin lymphoma
3. Patients who have received systematic clinical treatment.
4. Patients with measurable lesions, at least containing one effective evaluation of efficacy.
Exclusion Criteria
2. Patients who cannot obtain effective evaluation data of efficacy.
16 Years
ALL
No
Sponsors
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Ruijin Hospital
OTHER
Responsible Party
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Zhao Weili
Dean
Central Contacts
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Other Identifiers
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Shanghai Lymphoma Cohort
Identifier Type: -
Identifier Source: org_study_id