Alprostadil as an Adjuvant Therapy With Indirect Angiosomal Revascularization in Critical Limb Ischemia.

Sponsor
Assiut University (Other)
Overall Status
Unknown status
CT.gov ID
NCT04312555
Collaborator
(none)
30
18

Study Details

Study Description

Brief Summary

The aim of this study is to assess the efficacy of Alprostadil (Prostaglandin E2) as adjuvant therapy after failure of direct but indirect angiosomal revascularization in patients with critical limb ischemia.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

In large number of elderly patients aged between 50 and 75 years, the arterial disease is prevalent (1%-7%). It has a significant impact on the quality of life. Pain, fear of limb loss, increased inactivity, and poor lifestyle choices which finally ended by disability. Disability in turn makes communities and counties carry more efforts and charges.

The incidence of critical limb ischemia (CLI) is increasing, and diabetic patients are especially prone to developing ischemic and neuro-ischemic foot ulcers. Twelve to 25% of diabetic patients may develop a foot lesion over time. Diabetic patients often present with more extensive tissue loss compared to non-diabetic patients. The importance of revascularization of the lower limb in patients with CLI has been well established, and expedited revascularization is mandatory once an ischemic foot ulcer is detected.

Although there is still a role for surgical bypass, over the last several decades the use of endovascular techniques has become more frequent. This development has been made possible by the evolution of endovascular devices and operator skills. The less-invasive endovascular approach is the preferred treatment method, especially in the frail diabetic patient with multiple comorbidities. Incisional wound healing in diabetic patients can also be problematic. In both open and endovascular revascularization there is a clear difference of approach in patients with CLI caused by inflow disease (iliac, femoral, and popliteal disease) and those with (additional) infrapopliteal involvement. Whereas in above-the-knee disease, it is clear that flow in the stenotic or occluded segment needs to be re-established, in below-the-knee (BTK) disease, potentially three vessels can be revascularized, and this poses a therapeutic dilemma. Choosing the correct target for revascularization can present a critical, complex issue in challenging cases, especially when multilevel arterial disease is present. Revascularization can be accomplished by using two approaches: "complete" revascularization (one vessel is better than none, two to three vessels are better than one) or "wound-related" revascularization. With CLI, the healing of an ulcer is blood-flow-dependent and the goal of treatment should be to get the best possible blood supply to the foot (direct revascularization). In practice this is not always feasible, and in order to guide the choice of which BTK vessel should be revascularized, the angiosome concept has been proposed, based on the idea that specific anatomical regions are perfused by specific arteriovenous bundles.

Prostaglandins are potent vasoactive agents with wide variety of other actions - vasodilatation, fibrinolysis and inhibition of platelet aggregation. PG infusion therapy may show a promising results in patients where such new reconstructive procedures are not feasible or failed and also as an adjunctive when there is a residual ischemia after the revascularization procedures.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Efficacy of Alprostadil as an Adjuvant Therapy With Indirect Angiosomal Revascularization in Patients With Critical Limb Ischemia.
Anticipated Study Start Date :
Apr 1, 2020
Anticipated Primary Completion Date :
Apr 1, 2021
Anticipated Study Completion Date :
Oct 1, 2021

Outcome Measures

Primary Outcome Measures

  1. Patency [3 months]

    Maintaining vessel patency without restenosis or need for re-intervention

  2. Major Adverse Limb Events (MALE) [3 months]

    repeated endovascular therapy, surgical revision, or major amputation during follow up period

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Subject ≥ 40 years.

  • Subject with chronic limb ischemia [Rutherford classification 4, 5 & 6].

  • Subject failed to direct revascularization.

  • Subject is able and willing to comply with the protocol and to adhere to the follow-up requirements.

  • Subject has provided written informed consent.

Exclusion Criteria:
  • Subject's age less than 40.

  • Imminent or foreseeable amputation

  • Subject already had a major amputation on the affected extremity

  • Subject has emergent ischemic lesion [such as gas forming infection].

  • Subject has a known hypersensitivity or contraindication to anticoagulants, anti-platelets, or contrast media, which is not amenable to pre-treatment.

  • Subject has a known hypersensitivity or contraindication to Alprostadil.

  • Subject is not in the position to be primarily revascularized or refuses surgery.

  • Acute ischemia and peripheral vascular disorders of inflammatory or immunologic origin

  • Neuropathic or venous ulcers

  • Already using vasoactive medication or prostaglandins

  • Treatment with prostanoids within 3 months prior to inclusion

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Assiut University

Investigators

  • Principal Investigator: Ashraf Elnaggar, Dr, Assiut University
  • Study Chair: Hassan Bakr El-Badawy, Prof, Assiut University
  • Study Director: Mohamed Elsagheer Elhewwy, Prof, Al-Azhar University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Seif Eleslam Abdelhafiz Tawfik Ali, Resident doctor at Vascular & Endovascular surgery department, Assiut University
ClinicalTrials.gov Identifier:
NCT04312555
Other Study ID Numbers:
  • Alprostadil with CLI
First Posted:
Mar 18, 2020
Last Update Posted:
Mar 20, 2020
Last Verified:
Mar 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Seif Eleslam Abdelhafiz Tawfik Ali, Resident doctor at Vascular & Endovascular surgery department, Assiut University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 20, 2020