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Completed

NCT Number: NCT00485056

Pioglitazone on Cardiac Function and Large Arteries (PICCOLA Study)

This study aims to use a novel, sensitive, non-invasive scanning technique to investigate the effects of insulin-sensitizing agent pioglitazone, on heart and artery function.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

International Centre for Circulatory Health

London, W2 1PG, United Kingdom

About this study

The prevalence of diabetes mellitus and impaired glucose tolerance are nearing epidemic proportions in developed societies. For example in the USA >16 million individuals have diabetes and this number is predicted to double over the next two decades. Diabetes is a major risk factor for death and disability, primarily from cardiovascular disease (CVD).

The mechanisms of how diabetes increases the risk of developing CVD are not fully understood. It is evident from previous studies that diabetes has an adverse effect on both artery and heart function. What is emerging from recent studies is that it is likely that these proven dysfunctions in the arteries and heart interact to increase the risk of CVD.

Insulin-sensitizing agents, such as Pioglitazone, may have a beneficial effect on heart and artery function. This study aims to further our understanding of the effect of these agents on heart and artery using a novel, sensitive, non-invasive scanning technique to investigate the effects of this group of drugs on heart and artery function.

This is a prospective double-blind randomised crossover study comparing the insulin-sensitizing drug, Pioglitazone with a placebo in 24 volunteers. Following a >1 week run-in period subjects will be randomised double-blind to 1 of 2 treatment sequences. Subjects will either receive the active drug (Pioglitazone 45mg/day) for a 12 week period, followed by a 2 week washout and then the placebo drug for 12 weeks OR they will receive the placebo drug for 12 weeks, followed by the 2 week washout and 12 weeks of the active drug (Pioglitazone 45mg/day).

This design was chosen to test the null hypothesis that the active drug will have no effect on diastolic heart function. The use of a placebo is essential to ensure that any benefits found can be attributed to the active drug. The design also allows us to minimise the number of subjects needed and is the gold standard approach to avoid observer bias.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female of any age with Type 2 Diabetes

Exclusion criteria

  • Subjects will be excluded if they have any of the following:
  • Known coronary heart disease,
  • Patients receiving Insulin,
  • Uncontrolled hypertension (i.e. >160mmHg systolic or >95mmHg diastolic),
  • Systolic dysfunction (ejection fraction <50%),
  • Heart Valve Disease,
  • Proliferative or pre-proliferative retinopathy,
  • Severe hepatic or renal impairment.
  • Possible pregnancy
  • Malignancy

Treatment and study plan

pioglitazone

Drug

45mgs daily

Primary outcomes

  1. The primary endpoint will be the TDI E' ratio which is the relatively preload independent measure of ventricular diastolic function.

    Time frame: 26 weeks

Secondary outcomes

  1. E/E' measured by TDI (a non-invasive measure of preload).

    Time frame: 26 weeks

Sponsors and collaborators

Lead sponsor

Imperial College London

Other

Registry information

Official study title

Pioglitazone on Cardiac Function and Large Arteries (PICCOLA)

Acronym: PICCOLA

Important dates

Study start
2008
Primary completion
2010
Study completion
2010
First posted
Jun 12, 2007
Registry last updated
Aug 9, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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