Ignite Creation Date:
2024-05-06 @ 6:37 PM
Last Modification Date:
2024-10-26 @ 2:51 PM
Study NCT ID:
NCT05725213
Status:
COMPLETED
Last Update Posted:
2024-02-23
First Post:
2023-01-19
Brief Title:
ADL-PDT Under Routine Clinical Conditions in Patients With Actinic Keratosis
Sponsor:
Galderma Laboratorium GmbH
Organization:
Galderma Laboratorium GmbH
Study Overview
Official Title:
Non-interventional Study Investigating Photodynamic Therapy With Artificial Daylight Under Routine Clinical Conditions in Patients With Actinic Keratosis ArtLight
Status:
COMPLETED
Status Verified Date:
2024-02
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:
The objective of this non-interventional study NIS is to gain comprehensive insights into the practicability of ADL-PDT with Metvix in patients with actinic keratoses under real-world conditions
Detailed Description:
The objective of this non-interventional study NIS is to gain comprehensive insights into the practicability of ADL-PDT with Metvix in patients with actinic keratoses under real-world conditions Furthermore this NIS will document the efficacy satisfaction safety and tolerability of ADL-PDT with Metvix in routine use according to the label
The observational study is designed as a multicenter study covering all parts of Germany Participating investigators are dermatologists experienced in ADL-PDT with an adequate pool of patients with actinic keratoses The observation time per patient will comprise up to 6 months including up to 4 visits
The observational study is designed as a multicenter study covering all parts of Germany Participating investigators are dermatologists experienced in ADL-PDT with an adequate pool of patients with actinic keratoses The observation time per patient will comprise up to 6 months including up to 4 visits
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
True
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None