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Clinical Study on the Treatment of Senile Weakness Syndrome of Kidney Essence Deficiency Type with Dihuang Yinzi

Clinical Study on the Treatment of Senile Weakness Syndrome of Kidney Essence Deficiency Type with Dihuang Yinzi

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072582
Enrollment
Unknown
Registered
2023-06-19
Start date
2023-06-19
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

frailty

Interventions

control group:Basic treatment and care of Western medicine
treatment group:traditional Chinese medicine+Basic treatment and care of Western medicine

Sponsors

Huadong Hospital Affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ? Diagnosed as frailty syndrome through the frailty screening scale (The "FRAIL" Scale); ? Conforming to the syndrome of elderly frailty and kidney essence deficiency in traditional Chinese medicine; ? Patients aged between 60 and 90, regardless of gender; ? Conscious, without physical disabilities, able to cooperate; ? Voluntarily accept clinical trials and sign an informed consent form.

Exclusion criteria

Exclusion criteria: ? Long term bed rest; ? Patients with severe heart, brain, liver, kidney, hematopoietic, and immune system diseases, as well as those with implanted cardiac pacemakers; ? Patients with diabetes and poor blood glucose control (HbA1c>8.0%); ? Acute systemic infectious diseases; ? Severe osteoarthritis; ? Patients who have participated in other clinical trials within the past month.

Design outcomes

Primary

MeasureTime frame
SPECT cerebral blood flow perfusion imaging;EFS;

Secondary

MeasureTime frame
blood fat;Vitamin testing;Bone metabolism testing;Interleukin detection;TFN;RBP;SOD;TP,ALB;

Countries

China

Contacts

Public ContactXuehua Cheng

Huadong Hospital Affiliated to Fudan University

396305322@qq.com+86 136 4195 3369

Outcome results

None listed

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