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Phase 2 Completed N=24 Treatment

Study to Assess the Potential for Adrenal Suppression Following Treatment With DSXS in Patients With Atopic Dermatitis

Dermatitis, Atopic
Source: ClinicalTrials.gov NCT02595008 ↗
Enrolled (actual)
24
Serious AEs
0.0%
Results posted
Dec 2018
Primary outcomePrimary: Number of Participants With HPA Axis Suppression — 3; 1; 16; 3 Participants

Summary

this study is to evaluate the potential of DSXS to suppress HPA axis function in patients with moderate to severe atopic dermatitis.

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With HPA Axis Suppression
3; 1; 16; 3

Eligibility Criteria

Inclusion Criteria

  • Patients with a definite clinical diagnosis of stable atopic dermatitis

Exclusion Criteria

  • Patient is under the age of 2
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02595008). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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