Trial · NCT05976438
Skin Sodium and Salt Sensitivity of Blood Pressure
NCT05976438, Not applicable, Unknown, Cambridge University Hospitals NHS Foundation Trust
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Skin Sodium and Salt Sensitivity of Blood Pressure. Trials, record NCT05976438. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05976438
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Skin Sodium and Salt Sensitivity of Blood Pressure
- NCT number
- NCT05976438
- Status
- Unknown
- Phases
- Not applicable
- Enrollment
- 60 participants, estimated
- Lead sponsor
- Cambridge University Hospitals NHS Foundation Trust
- Conditions
- Hypertension
- Interventions
- Amlodipine, Chlortalidone
- First posted
- 2023-08-04
- Last updated
- 2023-08-04
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Concentration of Skin sodium | Approximately 8 weeks after receiving each treatment up to week 16 which will be the study completion week | This is planned for all participants |
| Primary | Concentration of Skin Potassium | Approximately 8 weeks after receiving each treatment up to week 16 which will be the study completion week | This is planned for all participants |
| Primary | Systolic blood pressure | All study visits - every 4 weeks up to week 16 which will be the study completion week | This is planned for all participants |
| Secondary | MRI skin sodium concentration | Approximately 8 weeks after receiving each treatment up to week 16 which will be the study completion week | This is planned for all participants |
| Secondary | Concentration of Skin glycosaminoglycans | Approximately 8 weeks after receiving each treatment up to week 16 which will be the study completion week | This is planned for all participants |
| Secondary | Diastolic blood pressure | All study visits - every 4 weeks up to week 16 which will be the study completion week | This is planned for all participants |
| Secondary | Body weight | Body weight measurement will be performed at baseline only. | This is planned for all participants |
| Other | Sodium MRI of kidney | Approximately 8 weeks after receiving each treatment up to week 16 which will be the study completion week | This is planned for patients who consent to sodium imaging of kidney |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
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 trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT05976438
GET https://conductscience.org/api/trials/v1/NCT05976438/registered