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Clinical Study on the Effects of Compound Glycyrrhizin Tablets on Maintenance Hemodialysis Patients

Clinical Study on the Effects of Compound Glycyrrhizin Tablets on Maintenance Hemodialysis Patients

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094823
Enrollment
Unknown
Registered
2024-12-27
Start date
2025-02-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

chronic kidney disease

Interventions

Control Group :Control Group: Routine hemodialysis treatment.
Treatment Group A :Treatment Group A: Low-dose group, 150 mg per day.
Treatment Group B:Treatment Group B: High-dose group, 225 mg per day.

Sponsors

Huashan Hospital Affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Gender: unrestricted; age > 18 years. 2. Maintenance hemodialysis patients with a dialysis duration of =6 months and =12 dialysis sessions, with minimal or no urine output. 3. Presence of pruritus caused by eczema or dermatitis. 4. No use of antibiotics within two weeks prior to enrollment, with a consistent diet maintained. 5. No history of nephrotic syndrome or cholestasis (as such patients have been shown to exhibit reduced 11ß-hydroxysteroid dehydrogenase activity).

Exclusion criteria

Exclusion criteria: 1. Patients who have recently taken probiotics. 2. Patients aged between 0 and 18 years.

Design outcomes

Primary

MeasureTime frame
TMAO;

Secondary

MeasureTime frame
Serum Biochemical Electrolytes;

Countries

China

Contacts

Public ContactXue Jun, Wu Yuanhao

Huashan Hospital Affiliated to Fudan University

xuejun@fudan.edu.cn+86 137 0195 5178

Outcome results

None listed

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