Creatine Safety & Tolerability in Huntington's Disease
Completed · Phase 2
Conditions studied: Huntington's Disease (HD)
In brief
The purpose of this study is to extend findings from the creatine dose-finding study (CREST-UP1) in Huntington's disease to evaluate the long-term safety, tolerability, and clinical impact of high dose creatine.
Key facts
- Study ID
- NCT01412151
- Run by
- Massachusetts General Hospital
- People needed
- 10
- Starts
- 2005-04-01
- Expected to finish
- 2011-11-01
- Last updated by the study team
- 2018-03-09
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Individuals who have completed the CREST-UP1 study.
- Individuals who are able to take oral medication.
- Individuals capable of providing informed consent and complying with trial procedures.
You may not qualify if…
- History of known sensitivity or intolerability to creatine.
- Clinical evidence of unstable medical illness in the investigator's judgment.
- Additional eligibility criteria apply.
Where it is running
- Massachusetts General Hospital — Charlestown, Massachusetts, United States
Full record on ClinicalTrials.gov
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