Condition (MeSH)
Bartter Syndrome
ClinicalTrials.gov lists 4 trials for Bartter Syndrome or a narrower condition beneath it.
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Trials per phase
4 of the 4 trials are tagged with Bartter Syndrome itself; the rest are tagged with a narrower condition beneath it.
When did Bartter Syndrome trials start? (3)
Shown in this order: most recent first, 1990 onwards. 2026 is partial: trials registered with a 2026 start date so far, not a full year.
Trials over time, by phase
- Not applicable
- Observational
Top of scale: 2
Trials registered with a start date in each year, 1990 onward, stacked by phase (complete years only; the current partial year is in the table's notes). The table below lists the same counts, most recent years first.
| Year | Trials started |
|---|---|
| 2019 | 1 |
| 2013 | 1 |
| 2009 | 2 |
No forecast is made for this condition: it averages 0.0 trial starts a year over the five years to September, under the 5 a year the method needs.
Recruitment duration, a model prediction: none of the 4 trials evaluated at the 2026-10-09 snapshot is predicted and still running. Source: ClinicalTrials.gov / AACT (CTTI), public domain.
What phase are Bartter Syndrome trials in? (2)
Shown in this order: phase order.
Show the trials by phase as a table
| Phase | Trials |
|---|---|
| Not applicable | 1 |
| Observational | 3 |
How many Bartter Syndrome trials are recruiting? (3)
Shown in this order: the order a trial moves through, from not yet recruiting to unknown.
| Status | Trials |
|---|---|
| Recruiting | 1 |
| Completed | 1 |
| Unknown status | 2 |
Status as registered on ClinicalTrials.gov. Each trial is counted once.
Which publications cover Bartter Syndrome? (5)
Shown in this order: major-topic papers first, then newest, then most linked to trials.
| Publication | Journal | Year | Major topic |
|---|---|---|---|
| A thiazide test for the diagnosis of renal tubular hypokalemic disorders. | Clinical journal of the American Society of Nephrology : CJASN | 2007 | Yes |
| Large-scale proteomics and phosphoproteomics of urinary exosomes. | Journal of the American Society of Nephrology : JASN | 2009 | No |
| Etiology of nephrocalcinosis in northern Indian children. | Pediatric nephrology (Berlin, Germany) | 2007 | No |
| Genetics of hereditary disorders of magnesium homeostasis. | Pediatric nephrology (Berlin, Germany) | 2004 | No |
| Magnesium deficiency: pathophysiologic and clinical overview. | American journal of kidney diseases : the official journal of the National Kidney Foundation | 1994 | No |
Prevalence (12)
Shown in this order: jurisdiction, then disease name. Orphanet observation for the mapped ORPHA concept; the mapping relation column says whether that concept is exactly this condition or broader or narrower.
| Orphanet disease | Type | Class | Geography | Jurisdiction | Mapping relation |
|---|---|---|---|---|---|
| Bartter syndrome | Point prevalence | Unknown | Worldwide | Not stated | Unspecified |
| Bartter syndrome | Annual incidence | 1-9 / 1 000 000 | Europe | Not stated | Unspecified |
| Bartter syndrome | Prevalence at birth | 1-9 / 100 000 | Kuwait | Not stated | Unspecified |
| Bartter syndrome | Annual incidence | 1-9 / 1 000 000 | Sweden | Not stated | Exact |
| Bartter syndrome | Annual incidence | 1-9 / 1 000 000 | Sweden | Not stated | Unspecified |
Showing 5 of 12 prevalence observations.
Rare-disease identity (2)
Shown in this order: exact, broader, narrower, other.
| Orphanet disease | ORPHA code | Relation | Source |
|---|---|---|---|
| Bartter syndrome | 112 | Exact | Orphadata Science knowledge files, Product 1 |
| Bartter syndrome | 112 | Exact | Orphanet Rare Disease Ontology (ORDO) |
Not on this page
Not measured: delivery record.
Checked, with nothing recorded for this condition: lead sponsors, serious adverse events in this condition's trials, and sub-conditions in mesh.
Not computed for conditions with fewer than 10 trials: drugs tested.