Trial Information
The Effect of Caphosol® on the Development of Esophagitis in Small Cell Lung Cancer (SCLC)Patients Treated With Concurrent Chemo/Radiotherapy A Prospective Study of Caphosol + Standard of Care Versus Standard of Care
Inclusion Criteria:
- 18 years or older
- Patients with histologically proven SCLC (all histological subtypes), treated with
concurrent chemo- and radiotherapy.
- Ability to understand the protocol and willing to provide written informed consent
Exclusion Criteria:
- Concurrent participation in a clinical trial in which the subject is taking or
receiving any investigational agent that may affect the frequency, severity or
duration of mucositis.
- Pre-existent esophagitis.
- Receiving investigational treatment for the prevention or treatment of mucositis.
- Prior irradiation to the lung or head and neck region.
Type of Study:
Interventional
Study Design:
Primary Purpose: Prevention
Outcome Measure:
number of patients with esophagitis
Outcome Time Frame:
3 months after the end of the Caphosolintervention
Safety Issue:
No
Authority:
Netherlands: Independent Ethics Committee
Study ID:
NL41938.015.12
NCT ID:
NCT01809756
Start Date:
Completion Date:
December 2016
Related Keywords:
- Small Cell Lung Cancer
- Esophagitis
- Lung Neoplasms
- Small Cell Lung Carcinoma