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Caffeine and Intermittent Claudication

Effects of Caffeine in Patients With Intermittent Claudication.

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00388128
Enrollment
80
Registered
2006-10-13
Start date
2006-09-30
Completion date
2009-09-30
Last updated
2011-06-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intermittent Claudication

Keywords

Intermittent Claudication, PAD, Caffeine, Walking capacity, ABI, QoL, Growth factor

Brief summary

The purpose of this study is to evaluate the change in Walking capacity after an intake of caffeine. The study design is cross-over and follow-up of 80 patients with leg pain caused by narrowing of their leg arteries, Peripheral Vascular Disease (PAD), stage II. Half of all will be revascularised, follow up will be after 3 months. It is hypothesized that caffeine (6mg/kg) can be a cheap, safe drug before walking exercise. Primary endpoint is maximum walking distance (MWD), treadmill-testing,(constant load, 0%,2m/h). Secondary endpoints are pain free walking distance (PWD), maximum muscle strength, endurance, reaction speed, balance, cognitive function, health related quality of life (SF-36).

Detailed description

PAD has a prevalence of 15-20 % in an elderly (\>50) western population. PAD can not be seen in isolation but represents the peripheral manifestation of a generalized artherosclerosis. The co-morbidity with coronary or cerebralartherosclerosis depends on the degree of severity of PAD, the relative risk of a death (predominantly cardiac) is increased by a factor 4. From af medical and a socio-economic point of view there is the need to control the PAD complication rate and related treatment costs as effectively as possible. The aim of any treatment of intermittent claudication is a clinically relevant improvement in the patient´s mobility and quality of life. There is agreement, that physical training does improve the collateralisation of vascular lesions, the rheologic properties of blood and lead to a shift from glycolytic to oxidative muscle fibers in the working musculature which increases the capillary density. The effect of physical training is also to modify the patients risk factor profile, even moderate training increase the insulin receptor sensitivity and the fibrinolytic activity and decrease the dLDL/HDL ratio and the diastolic blood pressure in hypertensive patients - and thereby decrease the overall cardiac mortality. This is a Phase 3, 12-week, double-blind, randomized, placebo-controlled cross-over and a follow-up study with 80 patients with intermittent claudication, half of which will be revascularized. The objectives of this study are to evaluate the efficacy of caffeine (6mg/kg)and the revascularisation procedure. The primary end-point will be maximal walking distance (MWD) in both groups of patients. Other efficacy measures will include claudication onset time (PWD), changes in Ankle Brachial Index (ABI), Quality of Life (QoL), cognitive function, plasma response of Vascular Endothelian Growth Factor (VEGF, FGF). Safety variables will include routine hematology parameters and adverse events.

Interventions

Capsules of caffeine 6 mg/kg, taken orally at each test. Before and after treadmill testing

Sponsors

Herning Hospital
CollaboratorOTHER
Central Jutland Regional Hospital
CollaboratorOTHER
University of Aarhus
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* men and women \> 40 years * history of IC of the lower extremities, Fontaine II * ankle-brachial index (ABI)\> 0.9 (subjects who are referred for a revasularizarition procedure)

Exclusion criteria

* dementia * diabetes * illness or reason to be unable to participate, f.ex. general weakness, amputation or arthritis * acute illness, f.ex. inflammation, unstable angina * other reasons which contraindicate participation/treadmill exercise * intake of Trental and/or Teofyllamin * weight \> 100kg

Design outcomes

Primary

MeasureTime frame
Quality of lifeduring test 1 and 3
Maximum walking distanceduring treadmill test

Secondary

MeasureTime frame
Endurance of 50%MVC kneeextensionAt end of each test
Postural stabilityin all tests
Reaction speedin all tests
Painfree Walking Distancetreadmill test
Walking Impairment Questionnairein first and third test
vascular endothelian growth factors VGF. FGFbefore and after 1. and 2. test
Cognitive functionin all tests
Max muscle strength (MVC) of kneeextensionAt end of each test

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026