Skip to content

Intervention study of Lycium ruthenicum on peripheral neuropathy patients with type 2 diabetes mellitus

Intervention study of Lycium ruthenicum on peripheral neuropathy patients with type 2 diabetes mellitus

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047239
Enrollment
Unknown
Registered
2021-06-11
Start date
2021-06-15
Completion date
Unknown
Last updated
2022-02-01

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

Conditions

Type 2 diabetic peripheral neuropathy

Interventions

Control group:No
Experimental group:Lycium ruthenicum Murr.was consumed 5g per person per day

Sponsors

Ningxia Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years; 2. Consistent with type 2 diabetes; 3. Consistent with diabetic peripheral neuropathy; 4. Duration of diabetes for at least 4 years; 5. Good blood sugar control, HbA1c 6.5%-7.5%; 6. The patient has agreed to participate in this study and has signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Neuropathy caused by other causes; 2. Pregnant women and lactating patients; 3. Patients with gastrointestinal diseases and small intestine surgery involved; 4. Patients with liver and kidney failure; 5. Patients who received Chinese herbal medicine, dietary supplements, neurological drugs (epalrestat, mecobalamin) and other treatments one month ago; 6. Patients with wolfberry allergy.

Design outcomes

Primary

MeasureTime frame
Nerve conduction velocity;nerve growth factor;

Secondary

MeasureTime frame
Malondiadehyde;C-reaction protein;

Countries

China

Contacts

Public ContactGao Qinghan

Ningxia Medical University

gaoqinghan85@126.com+86 18161506389

Outcome results

None listed

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