A Clinical Study on Efficacy & Safety Profile of Propionyl-L-carnitine Tablets for Peripheral Arterial Diseases (PLC)

This study has been completed.
Sponsor:
Collaborator:
Nanjing Medical University
Information provided by (Responsible Party):
Lee's Pharmaceutical Limited
ClinicalTrials.gov Identifier:
NCT00809497
First received: December 16, 2008
Last updated: March 28, 2012
Last verified: March 2008

December 16, 2008
March 28, 2012
May 2008
September 2009   (final data collection date for primary outcome measure)
To compare the difference between pre-and post-the treatment of each group [ Time Frame: 4 months ] [ Designated as safety issue: Yes ]
Same as current
Complete list of historical versions of study NCT00809497 on ClinicalTrials.gov Archive Site
Statistically describe the variance of ABI, CT and other indexes at the end of 4th month [ Time Frame: 4 months ] [ Designated as safety issue: Yes ]
Same as current
Not Provided
Not Provided
 
A Clinical Study on Efficacy & Safety Profile of Propionyl-L-carnitine Tablets for Peripheral Arterial Diseases
A Randomized, Multi-centre, Double-blind and Placebo Controlled Clinical Study of the Propionyl-L-carnitine Hydrochloride Tablets

The main objective of this study is to evaluate the effectiveness and safety of the propionyl-L-carnitine hydrochloride tablets among Chinese population in comparison with the placebo, for treatment of the peripheral arterial diseases (intermittent claudication) with oral supplementation of 2g daily for a 4 months continuous administration.

This is a randomized, multi-centre, double-blind and placebo controlled clinical study. Propionyl-L-Carnitine (PLC) is a kind of natural derivative of L-Carnitine (LC) and is produced in the body and concentrated by 90% in the skeletal muscle and myocardium via an enzyme-mediated reaction involving propionyl-CoA and LC. For oral adminsitration, PLC shows that the decrease of the leg muscle carnitine of the PAD patient appears to correlate with poor exercise performance. It has recently been shown that the severity of the impairment in walking distance is correlated with the impairment in carntine metabolism at the muscle level. 2g daily of PLC supplementation can significantly improve the walking ability in patients with IC with a maximum walking capacity between 50 and 250 meters on the treadmill.

Interventional
Phase 3
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
Peripheral Arterial Disease
Drug: Propionyl-L-carnitine Tablets
500mg tablets, oral administration of 2g daily
Other Name: DROMOS, ST261
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
239
January 2011
September 2009   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • The variability between the two standardized claudication tests during the wash-out period must be <20%, as assessed by the formular: (Highest MWD-Lowest MWD)/(Lowest MWDxx100%)
  • At the last visit during the wash-out period, the ABI at rest must be ,0.9

Exclusion Criteria:

  • with rest pain, ulceration, and/or gangrene
  • PAD of a non-atherosclerotic nature
  • Aortic or lower extremity arterial surgery, angioplasty, or lumbar sympathectomy within 6 months; any above ankle level amputation. Any type of major surgery during the last three months.
  • Except PAD, any concomitant disease that can limit patients' performance in the treadmill exercise.
  • with angina (at rest or activity) or any symptom which is sufficiently severe to discontinue the treadmill exercises.
  • Myocardial infarction within 6 months
  • Severe cerebral dysfunction
  • Type I diabetes (Stable type II diabetes can also be included)
  • alcohol or drug abused history within 3 months
  • Medium or severe anaemia (Hb,90g/L)
  • Platelets <100 x 10 9/L
  • Bleeding diathesis
  • Renal insufficiency or hepatic function laboratory test result>1.5 normal value
  • Treatment with LC or carnitien derivatives in the past 3 months
  • Pregnancy, lactation, fertility without adequate protest against pregnancy
  • Reject to sign the informed consent form
Both
40 Years to 75 Years
Yes
Contact information is only displayed when the study is recruiting subjects
China
 
NCT00809497
PLC-LZ00108, SFDA-2006L03870
Yes
Lee's Pharmaceutical Limited
Lee's Pharmaceutical Limited
Nanjing Medical University
Principal Investigator: Jianxin Li, MD Xuanwu hospital capital medical university
Lee's Pharmaceutical Limited
March 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP