Evaluation of Excessive UV Irradiation on Skin Aging by Multiphoton Laser Imaging and Biophysical Methods

NCT ID: NCT00372047

Last Updated: 2008-06-04

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

UNKNOWN

Study Classification

OBSERVATIONAL

Brief Summary

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

In this study, test persons with chronic excessive UV radiation and a control group are examined by multiphoton laser imaging and biophysical methods in order to evaluate the dermal fiber network. We expect to observe signs of advanced skin aging in the test group.

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.

Skin Aging

Study Design

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

Study Time Perspective

RETROSPECTIVE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

multiphoton laser imaging

Intervention Type DEVICE

Eligibility Criteria

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

Inclusion Criteria

* non smokers
* contraception
* 12 subjects with chronic excessive UV irradiation
* 12 normal subjects

Exclusion Criteria

* dermatological and other severe disorders
* pregnancy and lactation
* dermatological topical therapy
* internal medication
* cosmetical intervention at test area
Minimum Eligible Age

20 Years

Maximum Eligible Age

25 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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

University of Jena

OTHER

Sponsor Role lead

Principal Investigators

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

Martin Kaatz, Dr.

Role: PRINCIPAL_INVESTIGATOR

Dept. of Dermatology, FSU Jena

Locations

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

Department of Dermatology, FSU Jena

Jena, Thuringia, Germany

Site Status

Countries

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

Germany

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Johannes Koehler

Role: CONTACT

Phone: +49 3641 937359

Email: [email protected]

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Johannes Koehler

Role: primary

Other Identifiers

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

1845-08/06

Identifier Type: -

Identifier Source: org_study_id