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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01016080
Other study ID # COA840/2008
Secondary ID
Status Completed
Phase Phase 1
First received November 17, 2009
Last updated November 17, 2009
Start date February 2009
Est. completion date June 2009

Study information

Verified date November 2009
Source Chulalongkorn University
Contact n/a
Is FDA regulated No
Health authority Thailand: Ethical Committee
Study type Interventional

Clinical Trial Summary

Oral and intravenous glutathione have been used widely to whiten the skin. The investigators tested this hypothesis by giving oral glutathione for 4 weeks to medical students.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date June 2009
Est. primary completion date May 2009
Accepts healthy volunteers
Gender Both
Age group 18 Years to 25 Years
Eligibility Inclusion Criteria:

- Healthy medical students

Exclusion Criteria:

- history of skin cancer, especially melanoma

- consumption of any preparations containing glutathione within 1 month of enrollment

- pigmentary disorders or any dermatoses

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
glutathione
250 mg capsules, twice daily, orally
placebo
250 mg capsules, twice daily, orally

Locations

Country Name City State
Thailand King Chulalongkorn Memorial Hospital Bangkok

Sponsors (1)

Lead Sponsor Collaborator
Chulalongkorn University

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary Skin melanin index 4 weeks Yes
See also
  Status Clinical Trial Phase
Completed NCT04105504 - Oral Glutathione As A Skin Whitening Agent Phase 1