Effects of Epalrestat on Peripheral Neuropathy and Central Nervous System in Diabetic Patients

Sponsor
Xiangya Hospital of Central South University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05184049
Collaborator
(none)
72
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2
21
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Study Details

Study Description

Brief Summary

This study evaluated the efficacy of epalrestat in diabetic peripheral neuropathy and its effects on the central nervous system in diabetic peripheral neuropathy subjects.

Condition or Disease Intervention/Treatment Phase
Phase 4

Study Design

Study Type:
Interventional
Anticipated Enrollment :
72 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effects of Epalrestat on Peripheral Neuropathy and Central Nervous System in Diabetic Patient
Anticipated Study Start Date :
Jan 1, 2022
Anticipated Primary Completion Date :
Oct 1, 2023
Anticipated Study Completion Date :
Oct 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Epalrestat

oral epalrestat (50mg/ time, 3 times/day) + conventional hypoglycemia + oral mecobalamin (0.5mg/ time, 3 times/day) for half a year

Drug: Epalrestat,Mecobalamin
Epalrestat will be taken orally at a dose of 50mg 3 times a day before meals. In addition, conventional hypoglycemic and oral mecobalamin treatment 0.5mg/ time, 3 times/day, before meals.

Experimental: The control group

conventional hypoglycemia + oral mecobalamin (0.5mg/ time, 3 times/day) for half a year

Drug: Mecobalamin
Subjects takes mecobalamin 0.5mg orally, 3 times a day.Regular hypoglycemia.

Outcome Measures

Primary Outcome Measures

  1. The change of resting-state functional Magnetic Resonance Imaging [baseline , 6months]

    The change in grey matter volume,white matter area, local gyrification index after 6-months treatment

Secondary Outcome Measures

  1. Mean change of electromyography [baseline , 6months]

    mean change from baseline in nerve conduction velocity(m/s) after 6-months treatment

  2. Mean change of quantitative somatosensory testing [baseline , 6months]

    Mean change of temperature perception threshold(℃) after 6-months treatment

  3. Mean change of corneal confocal focus [baseline , 6months]

    Mean change of nerve fibre density(no./mm2) after 6-months treatment

  4. Mean change in HbA1c [baseline , 6months]

    Mean change of HbA1c(%) after 6-months treatment

  5. Change of Self-Rating Anxiety Scale [baseline , 6months]

    Mean change of Self-Rating Anxiety Scale score after 6-months treatment score.The minimum and maximum values is 25 and 100, which higher scores mean more anxiety.

  6. Change of Self-Rating Depression Scale [baseline , 6months]

    Mean change of Self-Rating Depression Scale score after 6-months treatment.The minimum and maximum values is 25 and 100, which higher scores mean more depression.

  7. Mean change of Toronto clinical scoring system [baseline , 6months]

    Mean change of Toronto clinical scoring system score after 6-months treatment.The minimum and maximum values is 0 and 19, which higher scores mean more severe neuropathy.

  8. Mean change of Neuropathic pain scale [baseline , 6months]

    Mean change of Neuropathic pain scale score after 6-months treatment.The minimum and maximum values is 0 and 10, which higher scores mean more severe neuropathy.

  9. Mean change of Michigan neuropathy screening form [baseline , 6months]

    Mean change of Michigan neuropathy screening form score after 6-months treatment.The minimum and maximum values is 0 and 23, which higher scores mean more severe neuropathy.

  10. Mean change of mini-mental state examination [baseline , 6months]

    Mean change of mini-mental state examination score after 6-months treatment.The minimum and maximum values is 0 and 30, which lower scores mean more severe cognitive dysfunction.

  11. Mean change of Montreal Cognitive Assessment [baseline , 6months]

    Mean change of Montreal Cognitive Assessment score after 6-months treatment.The minimum and maximum values is 0 and 30, which lower scores mean more severe cognitive dysfunction.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Patients aged 18 to 65 years (to the date of screening);

  2. A clear history of type 2 diabetes (using the 1999 WHO diabetes diagnostic criteria) with a course of disease > 6 months;

  3. HbA1c < 7%;

  4. Two or more of the following five tests are abnormal: abnormal temperature perception; Nylon wire for hypoesthesia or disappearance of the foot; Abnormal vibration sense; Ankle reflex disappeared; Two or more nerve conduction velocities were reduced;

  5. Have not used mecobalamin, epalrestat, lipoic acid or high-dose glucocorticoid in the recent (3 months) period, or have not been involved in other treatment of the same disease within 3 months prior to the study;

Exclusion Criteria:
  1. Neuropathy caused by other causes, such as cervical and lumbar lesions, cerebral infarction, etc.;

  2. With acute metabolic complications of diabetes, such as ketoacidosis, lactic acidosis, diabetes hyperotonic state, etc;

  3. Severe cardiovascular and cerebrovascular diseases , pulmonary heart disease or pulmonary insufficiency, renal failure, severe dyslipidemia, poorly controlled hypertension, severe hepatitis.

  4. Those with a history of malignant tumor or wasting diseases such as tuberculosis;

  5. Contraindications to MRI scanning: such as internal (especially oral) metal implants, claustrophobia, etc;

  6. Poor compliance or serious side effects;

  7. pregnant female.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Xiangya Hospital of Central South University Changsha Hunan China 410008

Sponsors and Collaborators

  • Xiangya Hospital of Central South University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Xiangya Hospital of Central South University
ClinicalTrials.gov Identifier:
NCT05184049
Other Study ID Numbers:
  • 20210406
First Posted:
Jan 11, 2022
Last Update Posted:
Jan 11, 2022
Last Verified:
Oct 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 11, 2022