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DERCOS DS DANDRUFF TREATMENT OBSERVATIONAL STUDY 2022

DERCOS DS DANDRUFF TREATMENT OBSERVATIONAL STUDY 2022

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05989633
Enrollment
5131
Registered
2023-08-14
Start date
2022-07-04
Completion date
2023-06-29
Last updated
2023-08-14

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

Conditions

Dandruff

Keywords

dandruff, treatment satisfaction

Brief summary

The aim of this study is to evaluate the satisfaction / tolerance / cosmeticity of Dercos DS

Interventions

OTHERDermocosmetic product: Selenium Disluphide Shampoo (Dercos DS)

to assess the benefit of Dercos DS in subjects with dandruff

Sponsors

Cosmetique Active International
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
12 Years to No maximum

Inclusion criteria

* Patients with dandruff or seborrheic dermatitis * All hair types * All ethnicities (Asian, Caucasian, Afro-American, African, Hispanic) * Including patients with specific occlusion habits (for instance veil use at least 8 hours per day, hat use) * Patients willing to provide written informed consent

Exclusion criteria

* Under 12 years old * Pregnancy, breast feeding, childbearing potential without adequate contraception, or irregular menstrual cycles. * History of allergy, anaphylaxis or hypersensitivity to any of the ingredients of Shampoo any of the ingredients of DERCOS ANTI-DANDRUFF normal to oily hair shampoo * History of allergic contact dermatitis secondary to shampoo, conditioner, mask, and/or leave-in. * Has any clinical manifestations in the treatment(s) or other disorders that, in the opinion of the investigator, may affect the evaluations or results of the study products.- Inability to stay the study period (56 days +-5 days) without performing any hair/scalp procedure, including coloring, straightening and cutting. * Inability to attend all study visits and follow treatment regimen

Design outcomes

Primary

MeasureTime frameDescription
DesquamationBaselineScale (0=absence to 4= very severe)
IrritationbaselineScale (0=absence to 4= very severe)
ErythemabaselineScale (0=absence to 4= very severe)
ItchingbaselineScale (0=absence to 10= very severe)
Area involvedbaselinescale from \<10% to \>90%
Tolerancebaselinescale from 0= none to 5=very tolerated
ImprovementDay 28scale from 0= worse to 5=very clearly improved
Impact of dandruff on patientbaselineScale from 0=not bothered at all to 5=very bothered
Global evaluation by investigatorDay 28Scale from 0=not at all satisfactory at all to 4=very satisfactory
Assessment of hair fiber and qualityDay 56scale from 0=worsened to 4=very improved
Product respect/protects hair fiberDay 56scale from 0=no, it is now more damaged/dry than before the treatment to 3=Yes, my hair fiber looks/feels better than before the treatment
Patient product efficacy satisfactionDay 28questionnare with scale ranging from 0=completely disagree to 5=completely agree
Patient product acceptabilityDay 28scale ranging from 0=not satisfied at all to 10=very satisfied
Patient global satisfactionDay 28scale ranging from 0=not satisfied at all to 10=very satisfied

Countries

Poland

Outcome results

None listed

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