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NOT YET RECRUITING
NCT06289959
NA

Plasma cfDNA Testing Guiding the Treatment Decisions of DLBCL

Sponsor: Second Affiliated Hospital of Soochow University

View on ClinicalTrials.gov

Summary

A prospective, single center, randomized, clinical controlled study to evaluate the efficacy and prognosis differences between precision treatment based on plasma cfDNA testing results and the current conventional diagnostic and treatment practices for DLBCL patients.

Official title: A Prospective, Single-Center, Randomized, Controlled Study Guiding the Treatment of Diffuse Large B-Cell Lymphoma Patients Based on Plasma cfDNA Testing

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2024-02-25

Completion Date

2029-01-01

Last Updated

2024-03-04

Healthy Volunteers

No

Interventions

DIAGNOSTIC_TEST

cfDNA

After achieving complete metabolic remission (Lugano response assessment criteria) following 6 cycles of R-CHOP-like chemotherapy, patients undergo plasma cfDNA testing upon enrollment,and the follow-up treatment plans are based on cfDNA results.

Locations (1)

The Second Affiliated Hospital of Soochow University

Suzhou, Jiangsu, China