Trial Outcomes & Findings for Efficacy and Safety of Salkera Emollient Foam in the Treatment of Moderate to Severe Keratosis Pilaris, a Prospective Study (NCT NCT00944216)
NCT ID: NCT00944216
Last Updated: 2022-02-04
Results Overview
TERMINATED
PHASE4
1 participants
12 weeks
2022-02-04
Participant Flow
Screening and recruitment occurred in June and July of 2009 in university dermatology clinic.
Participant milestones
| Measure |
Treatment
Salkera foam twice a day
|
|---|---|
|
Overall Study
STARTED
|
1
|
|
Overall Study
COMPLETED
|
1
|
|
Overall Study
NOT COMPLETED
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Efficacy and Safety of Salkera Emollient Foam in the Treatment of Moderate to Severe Keratosis Pilaris, a Prospective Study
Baseline characteristics by cohort
| Measure |
Treatment
n=1 Participants
Salkera foam twice a day
|
|---|---|
|
Age, Categorical
<=18 years
|
0 Participants
n=5 Participants
|
|
Age, Categorical
Between 18 and 65 years
|
1 Participants
n=5 Participants
|
|
Age, Categorical
>=65 years
|
0 Participants
n=5 Participants
|
|
Sex: Female, Male
Female
|
1 Participants
n=5 Participants
|
|
Sex: Female, Male
Male
|
0 Participants
n=5 Participants
|
|
Region of Enrollment
United States
|
1 participants
n=5 Participants
|
PRIMARY outcome
Timeframe: 12 weeksPopulation: This outcome was not assessed.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: 12 wksPopulation: This outcome was not assessed.
Subject disease severity score: None (0), mild (1), mild/moderate (2), moderate (3), moderate/severe (4), severe (5).
Outcome measures
Outcome data not reported
Adverse Events
Treatment
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Amy Chen, MD
Wright State University School of Medicine, Dept of Dermatology
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place