Clinical TrialID 5312
Combination Gel and Vascular ND in Mild to Moderate Rosacea
NCT01631656
Rosacea
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Record Fields
Scalar fields from the final clinical_trial record.
- Clinical Trial Id
- 5312
- Evidence Id
- 5312
- Core Evidence Id
- 5312
- Source Clinical Trial Id
- 5297
- Herb2 Clinical Trial Id
- HBCT005297
- Nct Id
- NCT01631656
- Title
- Combination Gel and Vascular ND in Mild to Moderate Rosacea
- Status
- Completed
- Phase
- Study Result
- Yes
- Study Condition
- Rosacea
- Study Type
- Interventional
- Study Design
- Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: SINGLE (OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
- Intervention
- DRUG: Azelaic acid|DEVICE: Nd:Yag laser
- Intervention Allocation
- Randomized
- Intervention Model
- Parallel
- Intervention Mask
- Single
- Intervention Purpose
- Treatment
- Gender
- All
- Age
- Adult, Older_Adult
- Enrollment
- 10
- Outcome Measure
- IGA of Improvement, Investigator's Global Assessment of severity integrates all lesions for overall score. This measure is commonly used as a quick and simple way to quantify disease severity both for clinical studies and in a non-study clinic setting. Score ranges from 0 = Clear or "No inflammatory signs of rosacea" to 6 = "Severe inflammatory signs of rosacea.", 6 weeks
- Sponsor Collaborator
- Wake Forest University Health Sciences|Bayer
- Funded By
- OTHER
- Location
- Wake Forest University Health Sciences Dept of Dermatology, Winston-Salem, North Carolina, 27104, United States
- Other Id
- IRB00012702
- Start Date
- 2010-07
- Primary Completion Date
- 2011-02
- Completion Date
- 2011-02
- First Posted
- 2012-06-29
- Results First Posted
- 2017-11-28
- Last Update Posted
- 2018-09-12
- Study Document
- Study Url
- https://clinicaltrials.gov/study/NCT01631656
- Title Cn
- Title En
- Combination Gel and Vascular ND in Mild to Moderate Rosacea
- Bilingual Status
- semi_complete