NCT00881348

CompletedPhase 4

Dermacyd Infantile (Lactic Acid) - Photo Evaluation.

Sanofi Source

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Other study identifiers

Sponsor study identifier

LACAC_L_04680

Study Type

interventional

Actual enrollment (reported)

25

Locations

1 country

Sites

1

Timeline

Study Start

February 2009

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

March 2009

Actual (reported)

Study Completion

March 2009

Actual (reported)

Brief Summary

Primary Objective: To demonstrate the absence of photo irritation and photosensitization potential of the product Dermacyd Infantile (Lactic Acid).

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 25 participants
Study completion date: March 2009
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Some registry-reported names shown below are not yet linked in this graph.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
February 2009
Date type not reported
This date has not been verified as actual or estimated.
Primary Completion
March 2009
Actual (reported)
Study Completion
March 2009
Actual (reported)
First Submitted
April 10, 2009
Actual (reported)
First Posted
April 15, 2009
Actual (reported)

Last Updated: April 15, 2009
Status Verified: April 2009
Last Update Submitted: April 14, 2009

Conditions

Hygiene

Outcome Measures

Primary Outcomes (1)

The photo irritation test and the photosensitivity will be measured using UVA irradiation and evaluated according International Contact Dermatitis Research Group (ICDRG) scale. The sensibility will be evaluated according to the skin type.
During 5 weeks (i.e. treatment period)

Study Arms (1)

Dermacyd infantile (Lactic Acid)

EXPERIMENTAL

5 weeks treatment

Drug: LACTIC ACID(ND)

Interventions

LACTIC ACID(ND)Drug

Dermacyd infantile (Lactic Acid)

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age18 Years - 60 Years

Sexall

Healthy VolunteersYes

Age GroupsAdult (18-64)

You may qualify if:

Phototype Skin I, II, III and IV
Integral skin test in the region

Sponsors & Collaborators

Sanofi
Industrylead

Study Sites (1)

Sanofi-Aventis Administrative Office

São Paulo, Brazil

Study Officials

Jaderson Lima
Sanofi
STUDY DIRECTOR

Enrollment

25 participants (actual enrollment reported by the registry).

Study Design

Study Type: interventional
Phase: phase 4
Allocation: NON RANDOMIZED
Masking: NONE
Purpose: SUPPORTIVE CARE
Intervention Model: SINGLE GROUP
Sponsor Type: INDUSTRY

Study Record Dates

First Submitted

April 10, 2009

First Posted

April 15, 2009

Study Start

February 2009

Date type not reported

This date has not been verified as actual or estimated.

NCT00932984

Dermacyd Silver Floral (Lactic Acid) - Photo Evaluation

Phase 3Completed

NCT00933075

Dermacyd Silver Frutal (Lactic Acid) - Photo Evaluation.

Phase 3Completed

NCT00933413

Dermacyd Silver Frutal (Lactic Acid) - Acceptability.

Phase 3Completed

NCT00933569

Dermacyd Silver Floral (Lactic Acid) - Acceptability.

Phase 3Completed

NCT00933907

Dermacyd PH_DESILSTY_FR (Lactic Acid) - Compatibility - Stay on Frutal

Phase 3Completed

NCT00933504

Dermacyd Silver Floral (Lactic Acid) - Compatibility - Stay on Floral

Phase 3Completed

Willingness in following the study procedures and to be present in the clinic at the days and scheduled time for medical evaluations and for application of occlusion.

You may not qualify if:

Use of Anti-inflammatory, immunosuppressant or anti-histaminic drugs
Lactation or gestation
Use of Anti-inflammatory drugs 30 days and/or immunosuppressant drugs during 3 months before the selection
Diseases which can cause immunity decrease, such as HIV, diabetes
Previous atopy
History of sensitivity or irritation for topic products
Active cutaneous diseases which can interfere in the study results
Use of new drugs and/ or cosmetics during the study
Cutaneous reactivity
Previous participation in studies, which had used the product
Volunteers who have immunodeficiency congenital or acquired.
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Contact the study team to confirm eligibility.

Primary Completion

March 2009

Actual (reported)

Study Completion

March 2009

Actual (reported)

Last Updated

April 15, 2009

Record last verified: 2009-04

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT00881348
Data provider: ClinicalTrials.gov
Source updated: 2009-04-15
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:21:34 UTC

Locations

BR(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

Primary Completion

Study Completion

First Submitted

First Posted

Conditions

Outcome Measures

Primary Outcomes (1)

Study Arms (1)

Dermacyd infantile (Lactic Acid)

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

Study Officials

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations