Neo-Synalar Modified 48 Hour Patch Test

PHASE4CompletedINTERVENTIONAL
Enrollment

206

Participants

Timeline

Start Date

June 30, 2014

Primary Completion Date

June 30, 2014

Study Completion Date

June 30, 2014

Conditions
Allergy
Interventions
DRUG

Neo-Synalar Cream

Approximately 0.2 g of test material is applied to the absorbent pad portion of a semi-occlusive dressing and applied as received to the upper back between the scapulae. The patches are applied to a designated treatment site and allowed to remain in direct skin contact for a period of 48 hours.

OTHER

Sodium Lauryl Sulfate Aqueous Solution (0.40%)

Approximately 0.2 ml of the positive , 0.40% aqueous solution of sodium lauryl sulfate is applied to the absorbent pad portion of a semi-occlusive dressing and applied as received to the upper back between the scapulae. The patches are applied to a designated treatment site and allowed to remain in direct skin contact for a period of 48 hours.

OTHER

Saline

Saline is applied to the absorbent pad portion of a semi-occlusive dressing and applied as received to the upper back between the scapulae. The patches are applied to a designated treatment site and allowed to remain in direct skin contact for a period of 48 hours.

Trial Locations (1)

07004

Michael Caswell PhD., CCRC,CCRA, Fairfield

All Listed Sponsors
lead

Noah Rosenberg, MD

INDUSTRY

NCT02168478 - Neo-Synalar Modified 48 Hour Patch Test | Biotech Hunter | Biotech Hunter