Trial · NCT04651088
Comparing Alkalinizing Agents Efficacy on Stone Risk in Patients on a Metabolically Controlled Diet
NCT04651088, Early phase 1, Not yet recruiting, University of Texas Southwestern Medical Center
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Comparing Alkalinizing Agents Efficacy on Stone Risk in Patients on a Metabolically Controlled Diet. Trials, record NCT04651088. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04651088
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Comparing Alkalinizing Agents Efficacy on Stone Risk in Patients on a Metabolically Controlled Diet
- NCT number
- NCT04651088
- Status
- Not yet recruiting
- Phases
- Early phase 1
- Enrollment
- 15 participants, estimated
- Lead sponsor
- University of Texas Southwestern Medical Center
- Conditions
- Kidney Stone
- Interventions
- Potassium citrate, Sodium bicarbonate, Litholyte, Crystal Lite, Potassium Bicarbonate
- First posted
- 2020-12-03
- Last updated
- 2026-02-13
Source ClinicalTrials.gov
Registered outcomes30
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | 24 hour urine volume | Change from baseline (Day 4) to initial start on treatment (Day 5) | Total urine volume |
| Primary | 24 hour urine volume | Change from baseline (Day 4) to end of study (day 12) | Total urine volume |
| Primary | 24 hour urine creatinine | Change from baseline (Day 4) to initial start on treatment (Day 5) | Urine creatinine |
| Primary | 24 hour urine creatinine | Change from baseline (Day 4) to end of study (day 12) | Urine creatinine |
| Primary | 24 hour urine calcium | Change from baseline (Day 4) to initial start on treatment (Day 5) | urine calcium |
| Primary | 24 hour urine calcium | Change from baseline (Day 4) to end of study (day 12) | urine calcium |
| Primary | 24 hour urine potassium | Change from baseline (Day 4) to initial start on treatment (Day 5) | Urine potassium |
| Primary | 24 hour urine potassium | Change from baseline (Day 4) to end of study (day 12) | Urine potassium |
| Primary | 24 hour urine sodium | Change from baseline (Day 4) to initial start on treatment (Day 5) | Urine sodium |
| Primary | 24 hours urine sodium | Change from baseline (Day 4) to end of study (day 12) | Urine sodium |
1 to 10 of 30Source ClinicalTrials.gov
See all 30 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.
Papers9
The papers the trial lists on ClinicalTrials.gov.
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/NCT04651088
GET https://conductscience.org/api/trials/v1/NCT04651088/registered?page=2