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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03293589
Other study ID # 00042158
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 1, 2017
Est. completion date October 30, 2017

Study information

Verified date March 2020
Source University Hospital Erlangen
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Treatment of patients with end-stage renal disease and critical limb ischemia still poses challenges to vascular medicine due to limited survival, comorbidities and infrapopliteal involvement of arteriosclerosis in these patients.

Most optimal vascular therapy mode has not been finally decided in these patients.

Therefore retrospective analysis of patients receiving open surgical and endovascular revascularisation was performed.


Description:

Query of internal clinical database for identification of patients (2009-2017)with end-stage renal disease and critical limb ischemia, receiving either open surgical (Group I "OR") or endovascular revascularisation (Group II "EVT").

Furthermore, retrospective comparison as to morphological criteria (lesion length, peripheral run-off, plantar arch) and comorbidities.

Prospective follow-up of identified patients by means of telephone contacts and/or clinical examination of evaluation of Long-term outcome measures (Overall survival, Amputation-free survival, wound healing)


Recruitment information / eligibility

Status Completed
Enrollment 77
Est. completion date October 30, 2017
Est. primary completion date September 20, 2017
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- presence of end-stage renal disease

- presence of critical limb ischemia (Ankle-brachial-index > 0.4 or presence of rest pain or ischemic ulcers or gangrene)

- revascularisation by means of Bypass or endovascular therapy

Exclusion Criteria:

- conservative Treatment

- non-atherosclerotic lesions

- coagulation disorders

Study Design


Intervention

Procedure:
open revascularization
surgical revascularization (i.e. Bypass surgery)
endovascular revascularization
endovascular revascularization (stent, ballon angioplasty)

Locations

Country Name City State
Germany University Hospital Erlangen Bavaria

Sponsors (1)

Lead Sponsor Collaborator
University Hospital Erlangen

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Amputation free survival Evaluation of limb salvage and survival as Composite endpoint 24 months
Secondary Overall survival Evaluation of Overall survival rate 24 months
Secondary Major Amputation Evaluation of Major Amputation rate 24 months
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