Trial · NCT05092854
The Effect of AMP Human Sodium Bicarbonate Lotion on Dehydrated Heat Stress
NCT05092854, 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 Dehydrated Heat Stress. Trials, record NCT05092854. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05092854
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 Dehydrated Heat Stress
- NCT number
- NCT05092854
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 18 participants, actual
- Lead sponsor
- University of Connecticut
- Conditions
- Fluid Retention, Sodium Retention, Heat Stress, Dehydration (Physiology), Renal Injury, Electrolyte and Fluid Balance Conditions
- Interventions
- PR Lotion - AMP Human Performance, Placebo Lotion, AminoVital - Rapid Recovery, Placebo Supplement
- First posted
- 2021-10-26
- Last updated
- 2022-10-24
Source ClinicalTrials.gov
Registered outcomes251
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Hydration Status - Change in Acute Urine USG | Phase-specific PRE Session | Assessment of hydration status via collection of urine USG |
| Primary | Hydration Status - Change in 24-h Urine USG | Phase-specific PRE Session | Assessment of hydration status via collection of urine USG |
| Primary | Hydration Status - Change in Acute Urine USG | Intervention Trial at the -45 minute mark | Assessment of hydration status via collection of urine USG |
| Primary | Hydration Status - Change in 24-h Urine USG | Intervention Trial at the -45 minute mark | Assessment of hydration status via collection of urine USG |
| Primary | Hydration Status - Change in Urine USG | Intervention Trial at the 0 minute mark | Assessment of hydration status via collection of urine USG |
| Primary | Hydration Status - Change in Urine USG | Intervention Trial at the 40 minute mark | Assessment of hydration status via collection of urine USG |
| Primary | Hydration Status - Change in Acute Urine USG | Intervention Trial at the 80 minute mark | Assessment of hydration status via collection of urine USG |
| Primary | Hydration Status - Change in Urine USG | Intervention Trial at the 220 minute mark | Assessment of hydration status via collection of urine USG |
| Primary | Hydration Status - Change in Urine USG | Rehydration Protocol - 3 hours post-intervention | Assessment of hydration status via collection of urine USG |
| Primary | Hydration Status - Change in Urine USG | Rehydration Protocol - 6 hours post-intervention | Assessment of hydration status via collection of urine USG |
1 to 10 of 251Source ClinicalTrials.gov
See all 251 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.
Tests2
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 |
| 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/NCT05092854
GET https://conductscience.org/api/trials/v1/NCT05092854/registered?page=2