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CompletedNCT05319275Updated Apr 8, 2022

Study of Acetyllevocarnitine Hydrochloride Tablets in Chinese Patients With Paresthesias Caused by DPN

A Phase 3 interventional study of Acetyllevocarnitine Hydrochloride Tablets and Placebo in Diabetic Peripheral Neuropathy (DPN) and Paresthesia, sponsored by Haisco Pharmaceutical Group Co., Ltd.. Completed at 34 sites in China. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2022-04-08.

Sponsored by Haisco Pharmaceutical Group Co., Ltd. · Phase 3, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year 7 months after the study started (first participant enrolled Jul 2020, registered Mar 2022).
Phase
Phase 3
Study type
Interventional
Enrollment
516
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
All
01

Study summary

The purpose of this study is to assess the efficacy of Acetyllevocarnitine Hydrochloride Tablets compared with placebo after 24 weeks, in chinese patients with paresthesia caused by Diabetic Peripheral Neuropathy (DPN).

Read the detailed description

This 24-week, multicentre, randomised, double-blind, placebo-controlled phase III study is to assess the efficacy and safety of Acetyllevocarnitine Hydrochloride Tablets in Chinese patients with paresthesia caused by DPN.The trial included a 2-week screening period, a 1-week placebo run-in period, a 24-week randomized treatment period, and a 2-week follow-up period.

02

Conditions studied

  • Diabetic Peripheral Neuropathy (DPN)
  • Paresthesia

Browse trials for

03

In context

Paresthesia

66 studies on the registry are indexed under Paresthesia; 14 are open to participants now.

This study's enrollment of 516 is above the median of 48 across 52 interventional studies indexed under Paresthesia.

Browse Paresthesia studies →

Lead sponsor

Haisco Pharmaceutical Group Co., Ltd. is the lead sponsor of 118 studies on the registry; 51 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age ≥ 18 and ≤ 70 years, Male and female patients;
  • Type 1 or 2 diabetes mellitus on hypoglycemic therapy for 3 months or more, and clinical diagnosis of DPN;
  • \< 9.0%;
  • Toronto Clinical Neuropathy Score ≥ 6 at screening and baseline.

Exclusion criteria

Exclusion Criteria:

  • Peripheral neuropathy caused by other diseases;
  • History of acute complications of diabetes within the past 6 months, such as diabetic ketoacidosis, diabetic hyperosmolar hyperglycemia syndrome or lactic acidosis, etc.;
  • Severe peripheral arterial disease; severe cardiopulmonary disease; or have a history of myocardial infarction, cerebrovascular accident or within 6 months before enrollment; or uncontrolled asthma or shortness of breath 2 months before enrollment; World Health Organization (WHO) cardiac function class III-IV; systolic blood pressure >160 mmHg or diastolic blood pressure >90 mmHg at screening;
  • Any infection at the screening visit that is not suitable for study participation;
  • (AST) or Alanine Transaminase (ALT) or total or creatinine > 2 times (ULN);
  • Known allergy to L-carnitine ingredients;
  • Severe systemic or psychiatric illness, history of epilepsy;
  • History of or antitumor therapy;
  • Severe bleeding disorder;
  • abnormalities in thyroid function tests;
  • Triglyceride >5.6 mmol/L;
  • Change of 2 points or more in the same item in mTCNS;
  • Nursing or pregnant women.
Terms in these criteria, in plain language(7)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

HbA1c

A blood test of average blood sugar over the past two to three months, given as a percentage or in mmol/mol. 6.5% (48 mmol/mol) or more is the usual threshold for diabetes, normally confirmed by a second test.

TIA (transient ischaemic attack)

A “mini-stroke”: temporary stroke-like symptoms caused by reduced blood flow to part of the brain, spinal cord or eye, without signs of a new stroke on a scan.

Stroke symptoms need emergency care at once, even if they go away.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

Bilirubin

A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.

Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
516 participants (actual)

Study arms

  • Experimental
    Acetyllevocarnitine Hydrochloride Tablets

    Drug: Acetyllevocarnitine Hydrochloride Tablets

  • Placebo comparator
    Placebo

    Drug: Placebo

Interventions

  • DrugAcetyllevocarnitine Hydrochloride Tablets

    500 mg (2×250 mg/tablet) after meal, 3 times per day

  • DrugPlacebo

    500 mg (2×250 mg/tablet) after meal, 3 times per day

06

What researchers measure

Primary outcomes

  1. mTCNS total score change from baseline at week 24

    Changes in Modified Toronto Clinical Neuropathy Score (mTCNS) total score from baseline at Week 24. Maximum mTCNS is 33, minimum is 0. And higher points mean more serious condition. However, more points drop from baseline mean a better outcome.

    Time frame: Baseline and week 24

Secondary outcomes

  1. mTCNS total score change from baseline at week 12

    Changes in Modified Toronto Clinical Neuropathy Score (mTCNS) total score from baseline at Week 12. Maximum mTCNS is 33, minimum is 0. And higher points mean more serious condition. However, more points drop from baseline mean a better outcome.

    Time frame: Baseline and week 12

  2. Changes in each item score of mTCNS from baseline at week 12 and week 24

    The mTCNS contains the 11 items that assess symptoms and signs, and each item maximum is 3 points, minimum is 0. And higher points mean more serious condition. However, more points drop from baseline mean a better outcome.

    Time frame: Baseline, Weeks 12 and 24

  3. TCNS total score change from baseline at week 12 and week 24

    Changes in Toronto Clinical Neuropathy Score (TCNS) total score from baseline at Week 12 and Week 24. Maximum TCNS is 19, minimum is 0. And higher points mean more serious condition. However, more points drop from baseline mean a better outcome.

    Time frame: Baseline, Weeks 12 and 24

  4. Numeric Rating Scale (NRS) score change from baseline at week 24

    Changes in Numeric Rating Scale (NRS) score from baseline at Week 24. Maximum NRS is 10, minimum is 0. And higher points mean more serious condition. However, more points drop from baseline mean a better outcome.

    Time frame: Baseline and week 24

  5. Changes in Nerve Conduction Velocity (NCV) from baseline at week 24

    Time frame: Baseline and week 24

  6. Changes in Nerve Conduction Amplitude from baseline at week 24

    Time frame: Baseline and week 24

07

Study locations

34 sites
  • Guangzhou First People's Hospital
    Guangzhou, Guangdong, China
  • Huizhou Central People's Hospital
    Huizhou, Guangdong, China
  • Affiliated Hospital of Zunyi Medical University
    Zunyi, Guizhou, China
  • Hainan Third People's Hospital
    Sanya, Hainan, China
  • Handan Central Hospital
    Handan, Hebei, China
  • Hebei Petro China Center Hospital
    Langfang, Hebei, China
  • The Fourth Affiliated Hospital of Harbin Medical University
    Harbin, Heilongjiang, China
  • Huaihe Hospital of Henan University
    Kaifeng, Henan, China
  • Kaifeng Traditional Chinese Medicine Hospital
    Kaifeng, Henan, China
  • Luoyang Third People's Hospital
    Luoyang, Henan, China
  • The First Affiliated Hospital of Henan University of Science and Technology
    Luoyang, Henan, China
  • Xinxiang First People's Hospital
    Xinxiang, Henan, China
  • Henan Provincial People's Hospital
    Zhengzhou, Henan, China
  • The Medical Group of Zhengzhou First People's Hospital
    Zhengzhou, Henan, China
  • The Second Affiliated Hospital of Zhengzhou University
    Zhengzhou, Henan, China
  • Taihe Hospital
    Shiyan, Hubei, China
  • Affiliated Hospital of Nantong University
    Nantong, Jiangsu, China
  • The Affiliated Hospital of Xuzhou Medical University
    Xuzhou, Jiangsu, China
  • Jiujiang Traditional Chinese Medicine Hospital
    Jiujiang, Jiangxi, China
  • The Fourth Affiliated Hospital of Nanchang University
    Nanchang, Jiangxi, China
  • Yichun People's Hospital
    Yichun, Jiangxi, China
  • Affiliated Hospital of Yanbian University
    Yanbian, Jilin, China
  • The First People's Hospital of Yinchuan
    Yinchuan, Ningxia Hui Autonomous Region, China
  • Binzhou Medical University Hospital
    Binzhou, Shandong, China
  • Qingdao Central Hospital
    Qingdao, Shandong, China
  • Weihai Central Hospital
    Weihai, Shandong, China
  • Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine
    Hangzhou, Zhejiang, China
  • The Second Affiliated Hospital of Wenzhou Medical University
    Wenzhou, Zhejiang, China
  • Beijing Hospital
    Beijing, China
  • Beijing Luhe Hospital, Capital Medical University
    Beijing, China
  • Beijing Pinggu Hospital
    Beijing, China
  • Chongqing People's Hospital
    Chongqing, China
  • Yongchuan Hospital of Chongqing Medical University
    Chongqing, China
  • Tianjin First Central Hospital
    Tianjin, China
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Jul 2020 to primary completion in Dec 2021, 16 months.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 22, 2022
First posted
Apr 8, 2022
StartActual
Jul 23, 2020
Primary completionActual
Dec 7, 2021
CompletionActual
Jan 25, 2022
Last update
Apr 8, 2022
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 8, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05319275
Responsible party
Sponsor
First posted
Apr 8, 2022
Start date
Jul 23, 2020
Primary completion
Dec 7, 2021
Completion
Jan 25, 2022
Last update
Apr 8, 2022

Study contacts

Lixin Guo
study chair · Beijing Hospital

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Mar 2022. You cannot join it, but the record below documents what was studied.

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