Trial · NCT04598386
The Effect of AMP Human Sodium Bicarbonate Lotion on Hydration
NCT04598386, Not applicable, Completed, University of Connecticut
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. The Effect of AMP Human Sodium Bicarbonate Lotion on Hydration. Trials, record NCT04598386. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04598386
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- The Effect of AMP Human Sodium Bicarbonate Lotion on Hydration
- NCT number
- NCT04598386
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 20 participants, actual
- Lead sponsor
- University of Connecticut
- Conditions
- Fluid Retention, Fluid Loss, Sodium Retention, Cognitive Change, Heat Exposure, Hyperhydration, Electrolyte and Fluid Balance Conditions
- Interventions
- PR Lotion - AMP Human Performance, Placebo Lotion
- First posted
- 2020-10-22
- Last updated
- 2021-10-14
Source ClinicalTrials.gov
Registered outcomes196
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Fluid Retention - Change in Expelled Urine Volume | Hydration Baseline Day 1 | Assessment of fluid retention via collection of urine volume |
| Primary | Fluid Retention - Change in Expelled Urine Volume | Hydration Baseline Day 2 | Assessment of fluid retention via collection of urine volume |
| Primary | Fluid Retention - Change in Expelled Urine Volume | Hydration Baseline Day 3 | Assessment of fluid retention via collection of urine volume |
| Primary | Fluid Retention - Change in Expelled Urine Volume | Intervention Trial (Day 4) at the -90 minute mark. | Assessment of fluid retention via collection of urine volume |
| Primary | Fluid Retention - Change in Expelled Urine Volume | Intervention Trial (Day 4) at the 0 minute mark. | Assessment of fluid retention via collection of urine volume |
| Primary | Fluid Retention - Change in Expelled Urine Volume | Intervention Trial (Day 4) at the 30 minute mark. | Assessment of fluid retention via collection of urine volume |
| Primary | Fluid Retention - Change in Expelled Urine Volume | Intervention Trial (Day 4) at the 60 minute mark. | Assessment of fluid retention via collection of urine volume |
| Primary | Fluid Retention - Change in Expelled Urine Volume | Intervention Trial (Day 4) at the 90 minute mark. | Assessment of fluid retention via collection of urine volume |
| Primary | Fluid Retention - Change in Expelled Urine Volume | Intervention Trial (Day 4) at the 120 minute mark. | Assessment of fluid retention via collection of urine volume |
| Primary | Fluid Retention - Change in Expelled Urine Volume | Intervention Trial (Day 4) at the 180 minute mark. | Assessment of fluid retention via collection of urine volume |
1 to 10 of 196Source ClinicalTrials.gov
See all 196 registered outcomesOutcomes0
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.
Tests3
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| Choice Reaction Time | Secondary outcome | ConductCognition |
| Go/No-Go Task | Secondary outcome | ConductCognition |
| Stroop Color-Word Test | Secondary outcome | ConductCognition |
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/NCT04598386
GET https://conductscience.org/api/trials/v1/NCT04598386/registered?page=2