Trial · NCT07887906
Registered outcomes22
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 20 of 22
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Measuring itch by computerized Visual Analog Scale Scoring | During Histamine/cowhage application | We will ask the subjects to rate the sensation of itch on a 100 mm VAS scale ranging from 0 to 100 where 0 indicates |
| Primary | Superficial blood perfusion | Before pruritogen application | |
| Primary | Superficial blood perfusion | 1 minute after pruritogen removal | |
| Primary | Superficial blood perfusion | 1 minute after cream+pruritogen removal | |
| Primary | Perception threshold tracking model (PTT) | Before cream application | |
| Primary | Perception threshold tracking model (PTT) | 1 minute after cream removal | |
| Secondary | Mechanically evoked itch (MEI) | 2 minute after pruritogen removal | MEI is measured by using mildly pruritic, non-painful von Frey nylon filaments of a predetermined intensity (generally 5-30 miliNewton of force). |
| Secondary | Mechanically evoked itch (MEI) | 2 minute after cream+pruritogen removal | MEI is measured by using mildly pruritic, non-painful von Frey nylon filaments of a predetermined intensity (generally 5-30 miliNewton of force). |
| Secondary | Mechanical Pain Thresholds (MPT) | 5 minute after pruritogen removal | This test is conducted using a pinprick set. The set consists of 7 needles each with a diameter of 0.6 mm and different force applications: 8, 16, 32, 64, 128, 256, and 512 mN. |
| Secondary | Mechanical Pain Thresholds (MPT) | 5 minute after cream+pruritogen removal | This test is conducted using a pinprick set. The set consists of 7 needles each with a diameter of 0.6 mm and different force applications: 8, 16, 32, 64, 128, 256, and 512 mN. |
| Secondary | Mechanical Pain Sensitivity (MPS) | 8 minute after pruritogen removal | This test is conducted with the same pinprick set used to test the MPT. |
| Secondary | Mechanical Pain Sensitivity (MPS) | 8 minute after cream+pruritogen removal | This test is conducted with the same pinprick set used to test the MPT. |
| Secondary | Cold Detection Thresholds (CDT) | 10 minute after pruritogen removal | The tests of thermal sensation will all be conducted using a TSA2 (Medoc Ltd, Israel) thermal sensory testing device |
| Secondary | Cold Detection Thresholds (CDT) | 10 minute after cream+pruritogen removal | The tests of thermal sensation will all be conducted using a TSA2 (Medoc Ltd, Israel) thermal sensory testing device |
| Secondary | Warm Detection Thresholds (WDT) | 10 minute after pruritogen removal | The tests of thermal sensation will all be conducted using a TSA2 (Medoc Ltd, Israel) thermal sensory testing device |
| Secondary | Warm Detection Thresholds (WDT) | 10 minute after cream+pruritogen removal | The tests of thermal sensation will all be conducted using a TSA2 (Medoc Ltd, Israel) thermal sensory testing device |
| Secondary | Cold Pain Thresholds (CPT) | 10 minute after pruritogen removal | The tests of thermal sensation will all be conducted using a TSA2 (Medoc Ltd, Israel) thermal sensory testing device |
| Secondary | Cold Pain Thresholds (CPT) | 10 minute after cream+pruritogen removal | The tests of thermal sensation will all be conducted using a TSA2 (Medoc Ltd, Israel) thermal sensory testing device |
| Secondary | Heat Pain Thresholds (HPT) | 10 minute after pruritogen removal | The tests of thermal sensation will all be conducted using a TSA2 (Medoc Ltd, Israel) thermal sensory testing device |
| Secondary | Heat Pain Thresholds (HPT) | 10 minute after cream+pruritogen removal | The tests of thermal sensation will all be conducted using a TSA2 (Medoc Ltd, Israel) thermal sensory testing device |
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/NCT07887906/registered