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NCT06795113

Optimization of 18F-FDG PET/CT Response Assessment and Prognostic Evaluation Strategies for High-Metabolism Lymphoma

Recruiting now Last updated 27 January 2025
What this trial tests

trial in Lymphoma in 4,000 participants. Currently enrolling.

Timeline
1 June 2013
Primary endpoint
31 December 2029
31 December 2029

Quick facts

Lead sponsorRuijin Hospital
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment4,000
Start date1 June 2013
Primary completion31 December 2029
Estimated completion31 December 2029
Sites1 location across China

Conditions studied

Sponsor

Ruijin Hospital

Who can join

Adults 18 to 100, any sex, with Lymphoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To develop a novel method for evaluating treatment response in lymphoma by utilizing PET/CT imaging data from patients with high-metabolic lymphoma. This involves comparing end-of-treatment PET (EOT-PET) with interim PET (iPET) results to establish a new response assessment approach. The aim is to contrast this method with the Lugano classification criteria, providing clinicians with more scientific and accurate tools for response evaluation and prognosis prediction.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Lymphoma

Currently open trials in the same condition.

Other Ruijin Hospital trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06795113.

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