Lactacyd Radiance (Lactic Acid) Prophetic Patch Test

Skin Irritation : Prophetic Patch Test of Lactacyd Radiance

Status

Completed

Phases

Phase 2

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00679562

Enrollment

200

Registered

2008-05-19

Start date

2008-03-31

Completion date

Unknown

Last updated

2009-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hygiene

Brief summary

Primay objective: To evaluate the potential of the products in eliciting adverse skin reaction.

Interventions

DRUGLactic Acid

Application of occlusive patches containing test product. For 24 hours and repeat 2 weeks later for participants with no reaction to Lactacyd Radiance

OTHERDistilled water

Application of patches containing distilled water for 24 hours

Study design

Allocation

NON_RANDOMIZED

Intervention model

CROSSOVER

Primary purpose

SUPPORTIVE_CARE

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to 60 Years

Healthy volunteers

Yes

Inclusion criteria

* Test area should have a healthy or normal skin * Individuals free of any systemic or dermatological disorder which, in the opinion of the investigative personnel would interfere with the study results or increase the risk of adverse reaction * Not currently use of steroid or any medication during the test

Exclusion criteria

* History of Allergy or Allergic Reaction to: * Hey Fever * Asthma * Poison Ivy * Food * Cosmetics * Soap * Detergent * Metal * Jewelry * Lather * Fabric * Medication The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Design outcomes

Primary

Measure	Time frame
Reaction after patch removal.	at 15-30 minutes and day 3

Countries

Thailand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026