Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT00371930
Other study ID # 1742-03/06
Secondary ID
Status Not yet recruiting
Phase Phase 1/Phase 2
First received September 1, 2006
Last updated June 2, 2008

Study information

Verified date June 2008
Source University of Jena
Contact Martin Johannes Köhler
Phone +49 3641 937359
Email johannes.koehler@med.uni-jena.de
Is FDA regulated No
Health authority Germany: Federal Institute for Drugs and Medical Devices
Study type Interventional

Clinical Trial Summary

24 test persons are treated with a dye suspension followed by a laser intervention. A decrease of hair density is expected.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- age 18-60

Exclusion Criteria:

- anormal behavior

- pregnancy

- pathologic skin conditions

- medication that my interfere with the study

- allergy against the photosensitizer

- lack of compliance

- other reasons considered important by the investigator

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind


Related Conditions & MeSH terms


Intervention

Procedure:
application of a dye suspension followed by a laser intervention


Locations

Country Name City State
Germany FSU Jena, Dept. of Dermatology Jena Thuringia

Sponsors (1)

Lead Sponsor Collaborator
University of Jena

Country where clinical trial is conducted

Germany, 

See also
  Status Clinical Trial Phase
Completed NCT02103608 - Clinical Evaluation of Silk'n Glide for Face N/A
Not yet recruiting NCT00495443 - Enhanced Safety Aesthetic Laser System N/A
Not yet recruiting NCT06003062 - Suppression of Upper Lip Hair Growth Using Novel Hemp Extract
Active, not recruiting NCT00145288 - Prospective Study of Patients With Hirsutism Phase 2/Phase 3
Completed NCT00152048 - Evaluation of Eflornithine on Facial and Forearm Skin Phase 4
Enrolling by invitation NCT01461694 - Facial Hair Reduction Using Intense Pulsed Light (IPL) & Alexandrite Laser Phase 2/Phase 3
Not yet recruiting NCT00441948 - Enhanced Safety Laser Hair Removal System N/A
Completed NCT03673995 - Myoinositol Plus L-tyrosine, Selenium and Chromium in PCOS N/A
Recruiting NCT04979377 - Prevalence of Hyperandrogenism in Type 1 Diabetes
Completed NCT02494297 - DUS on the Prescribing Indications for CPA/EE in 5 European Countries
Completed NCT00960310 - Relative Bioavailability Study of Bicalutamide 50 mg Tablet and Casodex Following a 50 mg Dose in Healthy Subjects Under Fed Conditions Phase 1
Completed NCT02793557 - Investigation of FOL-005 on Clinical Safety and Effect on Hair Growth Phase 1/Phase 2
Completed NCT01555190 - Combination Therapy With Myo-inositol and Folic Acid Versus Myo-inositol Alone N/A
Completed NCT01817894 - Treatment With Topical Eflornithin After Laser Treatment in Women With Facial Hirsutism Phase 4
Completed NCT00143052 - Bone Status and Insulin Resistance in Hirsutism N/A
Recruiting NCT01338519 - Database Study on Patients With PCOS N/A
Recruiting NCT04292587 - Prevalence of Hirsutism in Turkey: Data of The Dermatoendocrinology Study Group
Completed NCT00959335 - Relative Bioavailability Study of Bicalutamide 50 mg Tablet and Casodex Following a 50 mg Dose in Healthy Subjects Under Fasting Conditions Phase 1