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The correlational study between diabetics peripheral neuropathy and the metabolic mode of endogenic aldehyde and ketones that features 2,5-hexanedione

The correlational study between diabetics peripheral neuropathy and the metabolic mode of endogenic aldehyde and ketones that features 2,5-hexanedione

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100044320
Enrollment
Unknown
Registered
2021-03-16
Start date
2021-03-15
Completion date
Unknown
Last updated
2021-09-07

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

Conditions

Diabetic peripheral neuropathy

Interventions

DPN:N/A
DM without DPN:N/A

Sponsors

Shenzhen People Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged 45 to 60 years; 2. DPN group: patients with confirmed type 2 diabetes and confirmed diabetic peripheral neuropathy; 3. DM non-DPN group: patients with confirmed type 2 diabetes without typical signs and symptoms of diabetic peripheral neuropathy or abnormal nerve conduction function; 4. Healthy controls: non-diabetic or pre-diabetic patients with normal nerve conduction function.

Exclusion criteria

Exclusion criteria: 1. Presence of acquired non-specific inflammatory demyelinating peripheral neuropathy, including but not limited to: Grimballi syndrome, chronic inflammatory demyelinating polyradiculoneuropathy, etc. 2. Presence of peripheral neuropathy due to other systemic diseases, including but not limited to: 1) renal failure; 2) liver failure or cirrhosis; 3) heavy alcohol abuse; 4) tumours; 5) abnormal nail function; 6) connective tissue disease; 7) unstable disease of various causes; 8) HIV infection; 3. conditions that are temporarily unsuitable for NCS testing, including but not limited to: 1) diabetic foot; 2) gout; 3) osteoarthritis of the foot; 4) hyperthermia/hypothermia due to fever; 5) presence of severe lower limb vasculopathy; 6) mental anxiety or related psychiatric disorders; 7) lower limb oedema; 4. Pregnancy; 5. administration of aldolase reduction inhibitors, including epalrestat; 6. Other reasons for inability to participate in the study.

Design outcomes

Primary

MeasureTime frame
evaluation of peripheral neuropathy;blood glucose indices;Pyrrole adducts of 2,5-hexanedione;

Countries

China

Contacts

Public ContactYan Wu

Shenzhen People Hospital

chenxiao@szcdc.net+86 13802230166

Outcome results

None listed

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