New study aims to tame high potassium in kidney patients with standardized care
NCT ID NCT06884267
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tests whether a standardized care plan can help chronic kidney disease patients better control high potassium levels while optimizing their RAASi medications. About 1,000 participants will receive the care plan, which includes doctor training and patient education. The main goal is to see if more patients achieve normal potassium levels and optimal medication use after 48 weeks.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
Active substance
standardized hyperkalemia management implementation (clinical pathway and education)
What this could lead to
If successful, this could establish a practical, guideline-based care approach to help kidney disease patients better manage high potassium levels while optimizing their heart-kidney protective medications.
What could go wrong
This is an early-stage, single-arm study without a comparison group, so results may not prove the approach is better than usual care. Success depends on real-world adherence and may not apply to all patients.
Disclaimer
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
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Locations
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Research Site
Beijing, 100029, China
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Benxi, 117000, China
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Changchun, 130041, China
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Changsha, 410008, China
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Changsha, 410013, China
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Changsha, 410300, China
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Chengdu, 610031, China
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Chengdu, 610041, China
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Chengdu, 610078, China
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Chongqing, 400042, China
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Dalian, 116023, China
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Fuyang, 236600, China
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Fuzhou, 350005, China
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Fuzhou, 350031, China
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Gejiu, 661099, China
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Guangzhou, 510280, China
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Guangzhou, 510530, China
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Guiyang, 510630, China
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Haikou, 570311, China
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Hangzhou, 310006, China
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Hefei, 230001, China
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Hohhot, 10050, China
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Jinan, 250012, China
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Jinan, 250021, China
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Kunming, 650021, China
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Kunming, 650101, China
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Lanzhou, 730030, China
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Nanchang, 330006, China
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Nanning, 530021, China
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Nantong, 226001, China
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Ningbo, 315010, China
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Pingdingshan, 467000, China
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Qiqihar, 161000, China
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Shanghai, 200025, China
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Shanghai, 200032, China
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Shanghai, 200233, China
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Shenyang, 110001, China
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Shijiazhuang, 50051, China
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Taiyuan, 030001, China
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Tianjin, 300192, China
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Ürümqi, 830054, China
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Wuhan, 430022, China
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Wuhu, 241000, China
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Wuxi, 214062, China
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Xi'an, 710061, China
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Xining, 810001, China
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Xinxiang, 453100, China
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Yinchuan, 750004, China
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Zhengzhou, 450003, China