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Coverage: 2020-01-01 onwards, with up to 300 results per query from PubMed and Europe PMC and separate limits on other sources. This is a selected index, not a complete literature search.

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ICD E22.0ORPHA:963ACR

Acromegaly

Acromegaly is a rare hormonal disorder caused by excess growth hormone production, usually from a benign pituitary tumour. It leads to abnormal growth of hands, feet, and facial features, along with numerous systemic complications. An estimated 1,500 Australians live with acromegaly, and diagnosis is often delayed by a decade due to its gradual onset.

This overview is general information, not an individual medical assessment. Research is selected automatically and may include mismatches. How we select and explain research.

804
Articles
113
Trials (5 AU)
Data refreshed
19 October 2026
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Common Questions

What is Acromegaly?

Acromegaly is a rare hormonal disorder caused by excess growth hormone production, usually from a benign pituitary tumour. It leads to abnormal growth of hands, feet, and facial features, along with numerous systemic complications. An estimated 1,500 Australians live with acromegaly, and diagnosis is often delayed by a decade due to its gradual onset.

How many clinical trials are available for Acromegaly?

RareWays currently indexes 113 clinical trials for Acromegaly, of which 4 are actively recruiting. These counts cover indexed trials across countries, not just your country. An Australian site does not necessarily mean that site is recruiting. Check locations, eligibility and current availability with the study team.

Where does the research data for Acromegaly come from?

RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is refreshed automatically every day. All articles and trials link directly to their original sources.

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