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Molecular mechanisms and clinical standardization of difficult electrolyte abnormalities

Molecular mechanisms and clinical standardization of difficult electrolyte abnormalities

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300077004
Enrollment
Unknown
Registered
2023-10-26
Start date
2023-10-27
Completion date
Unknown
Last updated
2023-10-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

electrolyte abnormality

Interventions

Electrolyte abnormality:nil

Sponsors

Laibin People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with electrolyte abnormalities

Exclusion criteria

Exclusion criteria: (1) Long-term weight loss, anorexia, partiality, and other possible causes of electrolyte abnormalities; (2) Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
serum electrolyte profile;genetic testing;

Secondary

MeasureTime frame
24h urine electrolytes;Urinary potassium excretion rate;

Countries

china

Contacts

Public ContactShao-gang Ma

Laibin People's Hospital

mashaogang@163.com+86 191 5256 6300

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026