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NCT04633811 · ClinicalTrials.gov registry record · NA
Effect of Weight Loss on Urinary Oxalate Excretion in Obese Calcium Oxalate Kidney Stone Formers
A NA study of Kidney Stone, sponsored by University of Alabama at Birmingham.
- Active
- Registry status
- NA
- Development phase
- 14
- Enrollment target
- 1
- Study location
NCT04633811 is a NA study of Kidney Stone that is active but no longer recruiting, run by University of Alabama at Birmingham. The registered enrollment target is 14 participants, below the 192-participant average among 28 other Kidney Stone trials with a reported enrollment target (93% lower). The trial reports 1 study location across 1 state.
The verdict
NCT04633811, a NA study of Kidney Stone, is active but no longer recruiting, sponsored by University of Alabama at Birmingham.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 14 participants
- Enrollment target
- 1
- Study location
Study Summary
This protocol seeks to determine if weight reduction with the Optifast VLCD program leads to reduced contribution of endogenous oxalate synthesis and dietary oxalate absorption to the urinary oxalate pool in obese calcium oxalate stone formers.
Conditions Studied
Interventions
- DIETARY_SUPPLEMENT Low Oxalate Diet before Weight Loss
- DIETARY_SUPPLEMENT Oral load of oxalate and sucralose before Weight Loss
- DIETARY_SUPPLEMENT Optifast VLCD Program
- DIETARY_SUPPLEMENT Optifast VLCD Transition Phase
- DIETARY_SUPPLEMENT Low Oxalate Diet after Weight Loss
Study Locations (1)
Alabama
- University of Alabama at Birmingham - Birmingham
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 14 participants |
| Start Date | 2021-12-03 |
| Est. Completion | 2026-12-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04633811
The ClinicalTrials.gov registry entry for NCT04633811 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 14 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 192-participant average among 28 other Kidney Stone trials with a reported enrollment target (93% lower). The listed sponsor is University of Alabama at Birmingham, which has 1,160 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Kidney Stone appearing as the primary indexed condition, and to 5 interventions - of which Low Oxalate Diet before Weight Loss is the first listed.
NCT04633811 reports 1 study location spanning 1 distinct geographic area - top geographies include Alabama.
Frequently Asked Questions
What is clinical trial NCT04633811 about?
NCT04633811 is a clinical study titled "Effect of Weight Loss on Urinary Oxalate Excretion in Obese Calcium Oxalate Kidney Stone Formers". This protocol seeks to determine if weight reduction with the Optifast VLCD program leads to reduced contribution of endogenous oxalate synthesis and dietary oxalate absorption to the urinary oxalate pool in obese calcium oxalate stone formers.
What is the current status of trial NCT04633811?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 14 participants. The study started on 2021-12-03. Estimated completion is 2026-12-31.
What conditions does trial NCT04633811 study?
This clinical trial studies the following conditions: Kidney Stone.
What interventions are being tested in trial NCT04633811?
The interventions under investigation include: Low Oxalate Diet before Weight Loss (DIETARY_SUPPLEMENT), Oral load of oxalate and sucralose before Weight Loss (DIETARY_SUPPLEMENT), Optifast VLCD Program (DIETARY_SUPPLEMENT), Optifast VLCD Transition Phase (DIETARY_SUPPLEMENT), Low Oxalate Diet after Weight Loss (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT04633811?
This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04633811 being conducted?
This trial has 1 study location across Alabama. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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