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ACTIVE NOT RECRUITING
NCT04246203

Prognostic Role of Circulating Tumor DNA in Resectable Pancreatic Cancer

Sponsor: Ludwig-Maximilians - University of Munich

View on ClinicalTrials.gov

Summary

This is a non-randomized, multicenter, non-interventional study in patients with resectable PDAC. The patients are allocated to two observation groups according preoperative presence of ctDNA (Group A) or absence of detectable ctDNA (Group B) as determined in a liquid biopsy. After successful surgery of their pancreatic tumor and completion of local histological evaluation, tissue samples will be analyzed with regard to their mutational status with. Within 14 days before start of adjuvant tumor therapy another liquid biopsy will be taken to reassess the level of ctDNA after surgery. Patients will be monitored for disease recurrence according to harmonized, institutional standards using clinical, laboratory and (cross-sectional) imaging modalities. Accordingly, patients will be assessed every three months in the first eighteen months after surgery and every six months thereafter or based on clinical need for 36 months after the date of surgery Follow up will be documented until occurrence of relapse (or death if death occurs earlier than relapse/progression) for a maximum of 36 months after the date of surgery.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

200

Start Date

2021-12-12

Completion Date

2026-12-01

Last Updated

2025-03-11

Healthy Volunteers

No

Conditions

Interventions

OTHER

Liquid Biopsy

17-20 ml of blood will be collected prior of surgery and within 14 days before start of adjuvant chemotherapy.

Locations (6)

Ludwig Maximilians University Munich

Munich, Bavaria, Germany

Charité - Universitätsmedizin Berlin

Berlin, Germany

Uniklinik Köln

Cologne, Germany

Universitätsklinikum Hamburg-Eppendorf

Hamburg, Germany

Technische Universität München

Munich, Germany

Universitätsklinikum Ulm

Ulm, Germany