Viewing Study NCT00014066



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Last Modification Date: 2024-10-26 @ 9:06 AM
Study NCT ID: NCT00014066
Status: COMPLETED
Last Update Posted: 2013-02-05
First Post: 2001-04-10

Brief Title: Photodynamic Therapy Plus Brachytherapy in Treating Patients With Lung Cancer
Sponsor: Roswell Park Cancer Institute
Organization: Roswell Park Cancer Institute

Study Overview

Official Title: A Phase I Study of Photodynamic Therapy PDT Combined With High Dose Rate HDR Brachytherapy for Patients With Obstructive Bronchogenic Carcinoma
Status: COMPLETED
Status Verified Date: 2013-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: RATIONALE Photodynamic therapy uses light and drugs that make cnacer cells more sensitive to light to kill tumor cells Brachytherapy uses radiation to damage tumor cells Photodynamic therapy combined with brachytherapy may kill more tumor cells

PURPOSE Phase I trial to study the effectiveness of photodynamic therapy plus brachytherapy in treating patients with recurrent lung cancer that is blocking the lung passages
Detailed Description: OBJECTIVES I Determine the feasibility toxicity and effectiveness of combination therapy with Photofrin PDT and HDT brachytherapy in patients with endobronchial obstructions from lung cancer

OUTLINE This is not a randomized study Photofrin solution is administered slowly as a bolus injection over 3-5 minutes on day 1 Bronchoscopy is performed under general anesthesia 48 hours after Photofrin injection Light is transmitted from the laser to the tumor via quartz fiber optics interstitial or surface PDT Another bronchoscopy is performed 48 hours after PDT treatment to clean out any tissue debris left after PDT treatment HDR brachytherapy is performed using prescribed dose of radiation for 5-10 minutes to designated positions Repeat bronchoscopy is performed 3-4 weeks post HDR brachytherapy and a second HDR brachytherapy treatment may be given Patients are followed every 3 months until death or for 5 years

PROJECTED ACCRUAL 16 patients will be entered over 15 years

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
NCI-V97-1190 None None None
RPCI-DS-92-40 None None None