Success Metrics

Clinical Success Rate
100.0%

Based on 2 completed trials

Completion Rate
100%(2/2)
Active Trials
1(20%)
Results Posted
0%(0 trials)

Phase Distribution

Ph not_applicable
5
100%

Phase Distribution

0

Early Stage

0

Mid Stage

0

Late Stage

Phase Distribution5 total trials
N/ANon-phased studies
5(100.0%)

Highest Phase Reached

Unknown

Trial Status & Enrollment

Completion Rate

100.0%

2 of 2 finished

Non-Completion Rate

0.0%

0 ended early

Currently Active

1

trials recruiting

Total Trials

5

all time

Status Distribution
Active(2)
Completed(2)
Other(1)

Detailed Status

Completed2
Not yet recruiting1
Recruiting1
unknown1

Development Timeline

Analytics

Development Status

Total Trials
5
Active
1
Success Rate
100.0%
Most Advanced
N/A

Trials by Phase

N/A5 (100.0%)

Trials by Status

not_yet_recruiting120%
recruiting120%
unknown120%
completed240%

Recent Activity

1 active trials
Showing 5 of 5
not_yet_recruitingnot_applicable

Potassium Containing Salt-Substitute in Hemodialysis-Dependent End Stage Kidney Disease

NCT05558267
recruitingnot_applicable

Kidney-protective Intervention With Salt Substitute After Kidney Tumor Surgery

NCT07062952
completednot_applicable

Launching a Salt Substitute to Reduce Blood Pressure at the Population Level in Peru

NCT01960972
completednot_applicable

China Salt Substitute Study in Tibet

NCT01429246
unknownnot_applicable

Tibet Salt Reduction Study

NCT02021435

Clinical Trials (5)

Showing 5 of 5 trials
NCT05558267Not Applicable

Potassium Containing Salt-Substitute in Hemodialysis-Dependent End Stage Kidney Disease

Not Yet Recruiting
NCT07062952Not Applicable

Kidney-protective Intervention With Salt Substitute After Kidney Tumor Surgery

Recruiting
NCT01960972Not Applicable

Launching a Salt Substitute to Reduce Blood Pressure at the Population Level in Peru

Completed
NCT01429246Not Applicable

China Salt Substitute Study in Tibet

Completed
NCT02021435Not Applicable

Tibet Salt Reduction Study

Unknown

All 5 trials loaded

Drug Details

Intervention Type
DIETARY SUPPLEMENT
Total Trials
5