Trials / Completed
CompletedNCT03991936
Benefit of Placebo and Different Concentrations of Triamcinolone Acetonide in Nail Psoriasis
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 11 (actual)
- Sponsor
- Weill Medical College of Cornell University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This purpose of this study is to determine the lowest effective concentration of intralesional triamcinolone acetonide in the treatment of nail psoriasis.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Placebos | Normal saline intralesional injection |
| DRUG | Triamcinolone Acetonide 2.5 mg/mL | 2.5 mg/mL intralesional injection |
| DRUG | Triamcinolone Acetonide 5.0 mg/mL | 5.0 mg/mL intralesional injection |
| DRUG | Triamcinolone Acetonide 7.5 mg/mL | 7.5 mg/mL intralesional injection |
| DRUG | Triamcinolone Acetonide 10 mg/mL | 10 mg/mL intralesional injection |
Timeline
- Start date
- 2020-03-11
- Primary completion
- 2023-03-29
- Completion
- 2023-03-29
- First posted
- 2019-06-19
- Last updated
- 2024-03-27
- Results posted
- 2024-03-27
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03991936. Inclusion in this directory is not an endorsement.