Trial · NCT03313297
Registered outcomes18
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 18 of 18
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Skin 11β-HSD1 activity | Change between day 0 and day 28 | Enzyme activity radioassay to evaluate AZD4107 efficacy in skin |
| Secondary | Urinary cortisol / cortisone metabolites | Change between day 0 and day 35 | Urine samples for tetrahydrocortisol / tetrahydrocortisone metabolite ratios to evaluate systemic AZD4107 efficacy |
| Secondary | AZD4017 in plasma | Change between day 0 and day 28 | Quantification of AZD4017 concentration in plasma to evaluate systemic AZD4107 exposure |
| Secondary | AZD4017 in skin | Change between day 0 and day 28 | Quantification of AZD4017 concentration in plasma to evaluate skin AZD4107 exposure |
| Secondary | Discontinuation due to Adverse Event | Day 42 | Adverse Event-related participant withdrawals to evaluate safety |
| Secondary | Body mass index | Change between day 0 and day 35 | Body mass index to evaluate safety |
| Secondary | Waist-hip ratio | Change between day 0 and day 35 | Waist-hip ratio to evaluate safety |
| Secondary | Blood pressure (sphygmomanometer) | Change between day 0 and day 35 | Blood pressure to evaluate safety |
| Secondary | Sudomotor function | Change between day 0 and day 35 | Conducted with a Sudoscan device to measure c-fiber innervation in hands and feet for skin function |
| Secondary | Skin hydration | Change between day 0 and day 35 | Conducted with a Corneometer device to measure skin water content for skin function |
| Secondary | Epidermal barrier function | Change between day 0 and day 35 | Conducted with a Tewameter device to measure skin trans-epidermal water loss for skin function |
| Secondary | Epidermal barrier integrity | Change between day 0 and day 28 | Conducted by tape tripping to a pre-determined trans-epidermal water loss rate for skin function |
| Secondary | Skin thickness | Change between day 0 and day 35 | Conducted by Optical Coherence Tomography imaging for skin function |
| Secondary | Wound healing | Change between day 0 and day 2 | Conducted by Optical Coherence Tomography imaging for skin function |
| Secondary | Wound healing | Change between day 0 and day 7 | Conducted by Optical Coherence Tomography imaging for skin function |
| Secondary | Wound healing | Change between day 28 and day 30 | Conducted by Optical Coherence Tomography imaging for skin function |
| Secondary | Wound healing | Change between day 28 and day 35 | Conducted by Optical Coherence Tomography imaging for skin function |
| Secondary | Skin RNA-seq gene expression profiling | Change between day 0 and day 28 | For skin function |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT03313297/registered