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OpenTrials
Completed

NCT Number: NCT02941419

Treatment of PAD by Platelet Lysate for Therapeutic Angiogenesis

Induction of autologous angiogenesis in patients with critical limb ischemia using platelet lysate.

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Key information

About this study

Ten male and female patients diagnosed with Peripheral artery disease (PAD), will be recruited. This diagnosis will be based on medical history, physical examinations, laboratory tests, and specific diagnostic tests. Patients qualified for this study, are patients with distal extremity ischemia indicated by claudication and rest pain present for a minimum of 4 weeks without evidence of improvement in response to conventional drug therapy; showed angiographic evidence of PAD in the affected limb; and were not candidates for surgical revascularization. Platelet lysate will be injected intramuscularly at different sites of the gastrocnemius muscle. The purpose of this study is to evaluate the safety and efficacy of platelet lysate injections into ischematic limbs of patients with PAD.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Competent and willing to give informed consent, and to be available for all baseline treatment and follow up examinations required by the protocol.
  • Gender: Male or female.
  • Established Peripheral arterial disease, clinically and hemodynamically confirmed as per Rutherford 3, 4 and
  • History of intermittent claudication for > eight weeks.
  • Limited exercise due to moderate to severe claudication.
  • Resting ankle brachial index (ABI) < 0.85, toe pressure ≤ 60 mm Hg, Toe brachial index (TBI) <0.6, or Trans-cutaneous oxygen pressure (TcPO2) ≤ 60 mmHg in the foot.
  • Not eligible for surgical or radiological revascularization.
  • In case of diabetic patients, he/she should be on medication and fairly controlled (HbA1c <10%).
  • Normal liver enzymes, serum creatinine < 1.4
  • Normal platelet count.
  • On regular medication for hypertension if any.
  • No evidence of malignancy
  • Low Questionnaire scores.
  • Body mass index <30.

Exclusion criteria

  • Women with child bearing potential, pregnant and lactating women.
  • Rheumatoid Arthritis.
  • History of neoplasm or malignancy in the past 10 years.
  • Reported unstable cardiovascular disease, heart failure or symptomatic postural hypotension within 6 months before screening.
  • Leg edema
  • Inflammatory or progressive fibrotic disorder
  • Renal insufficiency or failure
  • History of infectious disorder.
  • Chronic inflammatory disease
  • History of stroke or myocardial infarction ( < 3 months).
  • Bleeding or clotting disorder, use of oral anticoagulant therapy (heparin, warfarin).
  • Lab values for
  • Hemoglobin <10 g/dl.
  • Platelet count <100,000.
  • Prothrombin time/ partial thromboplastin time (PT/PTT)> 3 seconds.
  • Alanine aminotrasferase (ALT) and aspartatet aminotrasferase (AST) > 1.5x of the normal lab value.
  • Creatinine ≥ 1.4
  • Poorly controlled diabetes (HbA1c ≥10)
  • Bilirubin > 1.5x of the normal lab value.
  • Systemic autoimmune disease.
  • Receiving immunosuppressant medications.
  • Uncontrolled hypertension or hypotension.
  • Abdominal aortic aneurism > 5 cm.
  • Active or untreated Tuberculosis.

Treatment and study plan

Platelet lysate

Biological

Autologous intramuscular platelet lysate injection for patients with peripheral arterial disease

Primary outcomes

  1. Assessment the safety of platelet lysate injection

    Time frame: 6 months

    Patients will be assessed for any relevant adverse event resulting from the platelet lysate injection

Secondary outcomes

  1. Assessment the efficacy of platelet lysate injection

    Time frame: 6 months

    Assessing the therapeutic benefit of all four platelet lysate injections by ankle brachial index (ABI).

Sponsors and collaborators

Lead sponsor

University of Jordan

Other

Registry information

Official study title

Safety and Efficacy of Platelet Lysate for Therapeutic Angiogenesis in Patients With Peripheral Arterial Disease

Important dates

Study start
2013
Primary completion
2016
Study completion
2017
First posted
Oct 21, 2016
Registry last updated
May 4, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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