CompletedPhase 2ACTRN12610000780055
Pioglitazone in the treatment of acromegaly
The effects on insulin-like growth factor 1 (IGF-1) and growth hormone levels using Pioglitazone in the treatment of active acromegaly
Sponsor
Auckland district health board
Enrollment
20 participants
Start Date
Jun 1, 2009
Study Type
Interventional
Conditions
Summary
To study the effects of pioglitazone (3 months at maximum dose of 45mg) on disease activity of acromegaly, as measured by IGF-1 level.
Eligibility
Sex: Both males and females
Inclusion Criteria1
- Active acromegaly - clinical features, elevated IGF-1 and/or non-suppressible growth hormone (>1mcg/L) after 75g oral glucose.
Exclusion Criteria6
- Initiation or discontinuation of octreotide in the last 6 months
- Initiation or discontinuation of cabergoline in the last 3 months if treatment caused >20% change in serum IGF-1
- Congestive heart failure (New York Heart Association (NYHA)Grade 2 or above)
- Current thiozolidinedione use
- Current malignancy
- Clinical liver disease
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Interventions
Pioglitazone - 1month run in period of 15mg (2 weeks) and 30mg (2 weeks)orally daily, then target dose of 45mg orally daily for further 3 months
Pioglitazone - 1month run in period of 15mg (2 weeks) and 30mg (2 weeks)orally daily, then target dose of 45mg orally daily for further 3 months
Locations(1)
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ACTRN12610000780055
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