Skip to content

Cobalamin deficiency in primary care: a placebo-controlled, double-blind, randomized trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN22063938
Enrollment
40
Registered
2006-02-20
Start date
2004-01-01
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cobalamin deficiency Nutritional, Metabolic, Endocrine Cobalamin deficiency

Interventions

Oral vitamin B12 versus placebo

Sponsors

Medical Outpatient Clinic, University of Lausanne (Switzerland)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients suspected of cobalamin deficiency with serum vitamin B12 level between 125 and 200 pmole/l. Patients with serum vitamin B12 level below 125 pmole/l were followed-up openly with oral cobalamin.

Exclusion criteria

Exclusion criteria: Unwillingness to participate

Design outcomes

Primary

MeasureTime frame
Evolution of biological markers (serum vitamin B12 level, serum methymalonic acid and homocystein levels)

Secondary

MeasureTime frame
Clinical evolution (hematologic, neurologic, psychiatric)

Countries

Switzerland

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026