Photodynamic Therapy of Actinic Keratoses With Alacare®

NCT ID: NCT01571336

Last Updated: 2016-09-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

388 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-04-30

Study Completion Date

2016-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study aims to collect data on the frequency of SCCs in the Alacare®-treated area during an interval of two years after Alacare®-PDT.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Actinic Keratosis

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Written informed consent
* Patients with 3 to 6 mild AK lesions on the hairless areas of the head and face which were treated with Alacare®-PDT according to the SPC
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

photonamic GmbH & Co. KG

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Peter Radny, MD

Role: STUDY_CHAIR

Dermatological group practice, Charlottenstraße 12, D-88045 Friedrichshafen, Germany

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Medizinisches Zentrum Bonn Friedensplatz

Bonn, , Germany

Site Status

Hautarztpraxis Prof. Kurzen

Freising, , Germany

Site Status

Hautärztliche Gemeinschaftspraxis Dr. med. Peter Dworzak Dr. med. Peter Radny

Friedrichshafen, , Germany

Site Status

Gemeinschaftspraxis Dres.Ina Röhrig-Petering und Holger Petering

Hildesheim, , Germany

Site Status

Dermatologische Gemeinschaftspraxis Prof. Dr. J. Gille & Dr. K. Spieth-Gille

Königstein im Taunus, , Germany

Site Status

ZENTderma

Mönchengladbach, , Germany

Site Status

Facharzt für Haut- und Geschlechtskrankheiten

Radolfzell, , Germany

Site Status

Praxis Prof. Dr. Thomas Dirschka

Wuppertal, , Germany

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Germany

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

NIS 01

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Actinic Keratosis Study
NCT02019355 COMPLETED EARLY_PHASE1