Trial Information
Current as of September 12, 2025
Enrolling by invitation
Keywords
ClinConnect Summary
The DESI - Düsseldorfer ESD Study is a prospective registry (observational study) in Germany that looks at how safe and effective Endoscopic Submucosal Dissection (ESD) is for removing certain gastrointestinal tumors that stay within the top layer of lining. It will collect information from about 1,000 adult patients with lesions in the esophagus, stomach, duodenum, colon, or rectum, to see how often the tumor can be removed in one piece with clean margins (an en-bloc, R0 resection), how often there are complications, and what the pathology shows after removal. The study will also track other outcomes such as complete endoscopic removal, whether the removal is considered curative under current guidelines, cases where no further treatment is needed after tumor-board review, and the rate of recurrence over time (up to about five years).
Participants are adults (18+ years) who need an ESD for a lesion in the GI tract and can give informed consent. The study uses real-world practice, so treatment decisions follow standard guidelines or discussions at a multidisciplinary tumor board. ESD is a specialized, longer procedure than some other endoscopic techniques and carries risks of complications during or after the procedure. If you participate, you can expect follow-up assessments over months to years to check margins, recurrence, and overall outcomes. The study is centered at Evangelisches Krankenhaus Düsseldorf in Germany, and it aims to improve safety, effectiveness, and patient selection for this advanced procedure.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • signed consent form
- • Indication for an ESD in the oesophagus, stomach, duodenum, colon or rectum
- • Age \>18 years
- Exclusion Criteria:
- • Age \< 18 years
About Torsten Beyna
Torsten Beyna is a dedicated clinical trial sponsor focused on advancing medical research and improving patient outcomes through innovative study designs and rigorous methodologies. With a commitment to ethical standards and regulatory compliance, Beyna orchestrates a diverse portfolio of clinical trials that span various therapeutic areas. By fostering collaborations with healthcare professionals, research institutions, and regulatory bodies, Torsten Beyna aims to accelerate the development of new therapies, ultimately enhancing the quality of care for patients worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Düsseldorf, Nrw, Germany
Patients applied
Trial Officials
Torsten PD Dr. med Beyna
Principal Investigator
Evangelisches Krankenhaus Düsseldorf
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported