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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02110251
Other study ID # PEARL study
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date September 2011
Est. completion date August 2014

Study information

Verified date July 2019
Source Catharina Ziekenhuis Eindhoven
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients with peripheral arterial disease with symptoms of critical ischemia or reduced tissue loss have a very high mortality and morbidity rate. So far, treatment strategies focused on the preservation of life and limb by an open surgical or endovascular revascularization, together with cardiovascular risk management and pain relief. Important modifiable factors related to mortality and morbidity are not covered in the current national and international guidelines. This study investigates the effects on mobility, mortality and quality of life with supplementation of the standard treatment of critical limb ischemia with supervised exercise therapy. Also a reduction of cardiovascular risk by intensive risk factor management and lifestyle coaching will be taken in to account. The supervised exercise therapy will take place under the supervision of a trained physiotherapist.


Recruitment information / eligibility

Status Terminated
Enrollment 14
Est. completion date August 2014
Est. primary completion date August 2014
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients with peripheral arterial disease Rutherford stage 4 and 5, where it is possible to improve the vascularization of the affected leg with the help of an endovascular and / or open surgical vascular intervention.

- Patients with both legs are affected, but the most severe leg does not exceed stage 5.

Exclusion Criteria:

- Severe cardiopulmonary comorbidity (NYHA 4) and previous amputations of lower leg or thigh.

- Patients with limited amputation of the toes can participate.

- Insufficient understanding of the Dutch language.

- No physiotherapy insurance.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Supervised Exercise Therapy


Locations

Country Name City State
Netherlands Medisch Centrum Alkmaar Alkmaar
Netherlands Catharina Ziekenhuis Eindhoven Noord-Brabant

Sponsors (1)

Lead Sponsor Collaborator
Catharina Ziekenhuis Eindhoven

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mobility Pain free walking distance WIQ ALDS 2 years
Secondary Quality of life RAND SF 36 2 years
Secondary Mortality 2 years