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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT04618536
Other study ID # 20-09-1037
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date October 5, 2020
Est. completion date January 31, 2021

Study information

Verified date November 2020
Source Indonesia University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Prolonged sunlight exposure in swimming athletes can cause various changes in the skin; among them is sunburn. The use of sunscreen can reduce sunburn effectively. However, various types of physical activity that can trigger sweating, friction, washing with water, or sun exposure after sunscreen use can interfere with its effectiveness in the form of a decreased SPF level. The purpose of this study is to determine and compare the persistence of organic and inorganic sun protection factor 30 (SPF 30) sunscreens after 1.5 hours of swimming.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 22
Est. completion date January 31, 2021
Est. primary completion date December 5, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - Female or male swimming athletes aged 18-40 years. - Practice swimming at least 3 times a week with a duration of 1.5-2 hours per practice in the morning or afternoon. - Willing to be the subject of research by signing the consent. - Do not have skin diseases. - Do not have a history of allergies to sunscreens. Exclusion Criteria: - Existence of skin lesion in the test area. - In the treatment of phototherapy. - Using drugs with photosensitivity side effects. - History of skin malignancy, history of photosensitivity reactions or history of disease affected by UV rays. - Exposure to direct sunlight to the test area 24 hours before the study and during the study period. - Absence of erythema response 24 hours after the radiation test. - Erythema occurs in the entire test area box 24 hours after the radiation test.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Inorganic sunscreen
Inorganic sunscreen will be applied evenly to 2 areas on the back of the subject with a 1 cc syringe and gloved finger in an amount of 2 mg / cm2. In the first session, one area will be irradiated 20 minutes after sunscreen application. In the second session, the other area will be irradiated after the subject has swam for 1.5 hours.
Organic sunscreen
Organic sunscreen will be applied evenly to 2 areas on the back of the subject with a 1 cc syringe and gloved finger in an amount of 2 mg / cm2. In the first session, one area will be irradiated 20 minutes after sunscreen application. In the second session, the other area will be irradiated after the subject has swam for 1.5 hours.

Locations

Country Name City State
Indonesia Cipto Mangunkusumo Hospital Jakarta DKI Jakarta

Sponsors (1)

Lead Sponsor Collaborator
Shannaz Nadia Yusharyahya

Country where clinical trial is conducted

Indonesia, 

Outcome

Type Measure Description Time frame Safety issue
Primary SPF change after swimming for 1.5 hours SPF of inorganic and organic sunscreen were calculated before and after swimming. The difference between SPF before and after swimming will be calculated and compared between the organic and inorganic group. SPF were calculated using minimal erythemal dose (MED) test. The test itself will be conducted in 2 days. Irradiation will be conducted on the first day and minimal erythemal dose result will be collected 24 hours after the irradiation. 24 hours
Secondary Inorganic sunscreen SPF SPF resulted from in vivo method, conducted before swimming. SPF were calculated using MED test. The test itself will be conducted in 2 days. Irradiation will be conducted on the first day and MED result will be collected 24 hours after the irradiation. 24 hours
Secondary Organic sunscreen SPF SPF resulted from in vivo method, conducted before swimming. SPF were calculated using minimal erythemal dose test. The test itself will be conducted in 2 days. Irradiation will be conducted on the first day and minimal erythemal dose result will be collected 24 hours after the irradiation. 24 hours
See also
  Status Clinical Trial Phase
Recruiting NCT00711256 - Sunscreen: Persistence of Sun Protection Factor and the Influence on Vitamin D N/A