Clinical trial Recruiting at 1 site Observational Ages 18 and up

Evaluating quality of life in esophageal cancer patients after chemoradiation

Official title: Prospective Observational Trial to Evaluate Quality of Life After Neoadjuvant or Definitive Chemoradiation in Patients With Esophageal Cancer

Run by Ludwig-Maximilians - University of Munich · NCT03712774 · Data updated 2026-11-12

This study is trying to see how treatment with chemoradiation affects the quality of life for people with esophageal cancer.

More Esophageal Cancer trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment60 (estimated)
SponsorLudwig-Maximilians - University of Munich
Academic / other
Locations1 site (Munich, Bavaria)
StatusRecruiting
StartedOctober 12, 2018
Main results expectedDecember 31, 2021
Study endsDecember 31, 2026
Registry record updatedOctober 19, 2018
Trial IDNCT03712774 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adults aged 18 and older with histologically proven esophageal cancer who are eligible for neoadjuvant or definitive chemoradiation.

Probably not a fit

Patients with distant metastases (except supraclavicular nodes), those receiving palliative treatment, or individuals with prior systemic treatment for esophageal cancer may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to assess the quality of life in patients with esophageal cancer who are undergoing neoadjuvant or definitive chemoradiation. Quality of life will be measured using standardized EORTC questionnaires, while also evaluating acute and late toxicities, functional outcomes, and oncological results. The study will track local and distant control, freedom from treatment failure, and overall survival, with planned correlations between patient and physician assessments of functional outcomes.

Why it matters

Potential benefit: If successful, this study could provide valuable insights into the quality of life and treatment outcomes for patients with esophageal cancer undergoing chemoradiation.

How similar studies have gone: While this approach is observational, similar studies evaluating quality of life in cancer patients have shown promising results, indicating the potential for meaningful insights.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* histologically proven esophageal Cancer (SCC or adenocarcinoma) without distant metastases (except supraclavicular nodes)
* indication for neoadjuvant or definitive chemoradiation using either cisplatin/5-FU or carboplatin/paclitaxel with curative intent
* age \>= 18 years
* written informed consent
* ability to answer the standardized questionaires according to the treating physician

Exclusion Criteria:

* age \< 18 years
* Treatment with palliative intent
* distant metastases (except supraclavicular nodes)
* second malignancy
* Prior systemic treatment for esophageal Cancer
* Treatment in an interventional study

Where it's running

  • Department of Radiation Oncology, University Hospital, LMU Munich
    Munich, Bavaria, Germany
    Recruiting

Study contacts

  • Principal investigator: Falk Roeder, MD — Ludwig-Maximilians Universität München
  • Study coordinator: Falk Roeder, MD
  • Email: Falk.Roeder@t-online.de
  • Phone: +49 89 4400

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.