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Clinical Trials/ISRCTN76180797
ISRCTN76180797
Completed
Not Applicable

A comparison of upper-limb and lower-limb exercise training in patients with intermittent claudication (IC)

Sheffield Hallam University (UK)0 sites104 target enrollmentOctober 25, 2005

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Peripheral arterial disease.
Sponsor
Sheffield Hallam University (UK)
Enrollment
104
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 25, 2005
End Date
TBD
Last Updated
11 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Sheffield Hallam University (UK)

Eligibility Criteria

Inclusion Criteria

  • Patients with stable intermittent claudication were recruited from the Sheffield Vascular Institute at the Northern General Hospital, Sheffield, UK. The clinical diagnosis of PAD was established using the patient?s history and a physical examination, and was confirmed by the Doppler assessment of ankle\-brachial pressure index (ABPI), a non\-invasive reliable measure of lower\-extremity hemodynamics, in accordance with current UK medical practice.

Exclusion Criteria

  • Patients experiencing symptoms of IC for less than 12 months, or reporting a significant change in walking ability within this time period were considered to have unstable disease and were, as a consequence, excluded. Patients were also excluded if they exhibited features of critical ischemia, had undergone a re\-vascularization procedure within the previous 12 months, or if initial assessment established that they suffered from severe arthritis (i.e. if they were unable to walk unaided or perform either upper\- or lower limb cranking exercise due to joint pain), severe lumbar spine disease or unstable cardiorespiratory conditions (i.e. unstable blood pressure, recent electrocardiographic changes or acute myocardial infarction, unstable angina, third\-degree heart block, acute congestive heart failure and severe respiratory conditions).

Outcomes

Primary Outcomes

Not specified

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