Clinical trial
Examining the Commonness of the C677T Mutation in the MTHFR Gene in Subjects With B12 Deficiency and the Influence of the B12 Deficiency Combined With the C677T Mutation on the MTHFR Gene on Endothelial Function.
NCT00730574 is registered in ClinicalTrials.gov with Moshe Flugelman as lead sponsor.
Search trials, sites, companies and investigators, and follow each one to the others. Individual plan, $249/seat/mo. Card required.
Registry record
As filed in ClinicalTrials.gov.
- Title
- Examining the Commonness of the C677T Mutation in the MTHFR Gene in Subjects With B12 Deficiency and the Influence of the B12 Deficiency Combined With the C677T Mutation on the MTHFR Gene on Endothelial Function.
- Lead sponsor
- Moshe Flugelman
- Phase
- Not applicable
- Overall status
- Terminated
- Start date
- July 31, 2008
- Completion date
- January 31, 2012
- Enrollment
- 100 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
b12 deficiency combined with c677t mutation on mthfr gene