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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03352323
Other study ID # PRG-NY-17-013
Secondary ID
Status Completed
Phase Phase 3
First received
Last updated
Start date October 18, 2017
Est. completion date March 30, 2018

Study information

Verified date November 2021
Source Padagis LLC
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the study will measure the decrease in redness on the face of rosacea subjects


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date March 30, 2018
Est. primary completion date December 6, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Male or non-pregnant, non-lactating female, 18 years of age or older. 2. Signed informed consent form that meets all criteria of current Food and Drug Administration regulations. 3. Females of childbearing potential must not be pregnant or lactating. 4. Females of childbearing potential must agree to the use of a reliable method of contraception throughout the study. 5. Have clinical diagnosis of rosacea with persistent (non-transient) facial erythema. 6. Have < 3 inflammatory lesions on the face. 7. Have an erythema score of 3 (moderate) or 4 (severe) for both the CEA and the PSA that is reflective of the overall targeted areas. 8. Willing to minimize external factors that might trigger rosacea flare-ups (e.g., spicy foods, hot drinks, hot environments, prolonged sun exposure, strong winds, emotional stress and alcoholic beverages) during the study. Exclusion Criteria: 1. Forms of rosacea that, in the opinion of the Investigator, would interfere with the diagnosis or assessment of study endpoints 2. Patient has a skin condition that, in the opinion of the Investigator, would interfere with the diagnosis or assessment of rosacea 3. Patients with active sunburn or excessive facial hair such as beards, sideburns, moustaches, etc. 4. Patients with moderate to severe telangiectasial masses 5. History of blood dyscrasia. 6. Significant history or current evidence of any uncontrolled chronic or serious disease or medical condition that would, in the judgment of the Investigator, would put the subject at undue risk or compromise the study assessments. 7. History or current evidence of Raynaud's syndrome, severe, unstable or uncontrolled cardiovascular disease, orthostatic hypotension, uncontrolled hypertension or hypotension, thromboangiitis obliterans, cerebral or coronary insufficiency, renal or hepatic or renal impairment, scleroderma, Sjögren's syndrome, depression, or narrow-angle glaucoma to an extent that, in the opinion of the Investigator, would place the subject at undue risk. 8. Female patients taking hormonal contraceptives or oral estrogen for less than one month or those that plan to change the dosage regimen during the course of the study. 9. Previous participation in this study. 10. Employees of the Investigator or research center or their immediate family members. 11. Inability to understand the requirements of the study and the relative information and are unable or not willing to comply with the study protocol.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Oxymetazoline
RLD

Locations

Country Name City State
United States J&S Studies College Station Texas

Sponsors (1)

Lead Sponsor Collaborator
Padagis LLC

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Responder Responder is defined as a 2-grade improvement from pre-dose on Day 1 on both the Clinician Erythema Assessment and Patient Self Assessment scales Day 15
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