Caffeine and Intermittent Claudication

This study has been completed.
Sponsor:
Collaborators:
Herning Hospital
Viborg Hospital
Information provided by:
University of Aarhus
ClinicalTrials.gov Identifier:
NCT00388128
First received: October 12, 2006
Last updated: June 8, 2011
Last verified: June 2011

October 12, 2006
June 8, 2011
September 2006
May 2009   (final data collection date for primary outcome measure)
  • Quality of life [ Time Frame: during test 1 and 3 ] [ Designated as safety issue: No ]
  • Maximum walking distance [ Time Frame: during treadmill test ] [ Designated as safety issue: No ]
  • Quality of life
  • Maximum Walking Distance
  • Increased level of endothelian growth factors: VGF, FGF
Complete list of historical versions of study NCT00388128 on ClinicalTrials.gov Archive Site
  • Painfree Walking Distance [ Time Frame: treadmill test ] [ Designated as safety issue: No ]
  • Max muscle strength (MVC) of kneeextension [ Time Frame: At end of each test ] [ Designated as safety issue: No ]
  • Endurance of 50%MVC kneeextension [ Time Frame: At end of each test ] [ Designated as safety issue: No ]
  • Postural stability [ Time Frame: in all tests ] [ Designated as safety issue: No ]
  • Reaction speed [ Time Frame: in all tests ] [ Designated as safety issue: No ]
  • Cognitive function [ Time Frame: in all tests ] [ Designated as safety issue: No ]
  • Walking Impairment Questionnaire [ Time Frame: in first and third test ] [ Designated as safety issue: No ]
  • vascular endothelian growth factors VGF. FGF [ Time Frame: before and after 1. and 2. test ] [ Designated as safety issue: No ]
  • Painfree Walking Distance
  • Strength of kneeextension
  • Endurance of 50%MVC kneeextension
  • Postural stability
  • Reactiontime
  • Cognitive function
  • Walking Impairment Questtionaire
Not Provided
Not Provided
 
Caffeine and Intermittent Claudication
Effects of Caffeine in Patients With Intermittent Claudication.

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).

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.

Interventional
Phase 3
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Crossover Assignment
Masking: Double Blind (Subject, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Intermittent Claudication
Drug: Caffeine 6mg/kg
Capsules of caffeine 6 mg/kg, taken orally at each test. Before and after treadmill testing
Placebo Comparator: A
Intervention: Drug: Caffeine 6mg/kg
Momsen AH, Jensen MB, Norager CB, Madsen MR, Vestersgaard-Andersen T, Lindholt JS. Randomized double-blind placebo-controlled crossover study of caffeine in patients with intermittent claudication. Br J Surg. 2010 Oct;97(10):1503-10.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
80
September 2009
May 2009   (final data collection date for primary outcome measure)

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
Both
40 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Denmark
 
NCT00388128
2006-001902-10, 2006/168
Yes
Regional Hospital Herning, Surgical Research Unit
University of Aarhus
  • Herning Hospital
  • Viborg Hospital
Principal Investigator: Anne-Mette H Momsen, MPH, Phys, ph.D stud Herning Hospital
University of Aarhus
June 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP