|
Home
Search
Study Topics
Glossary
|
![]() |
![]() |
|
![]() |
|
![]() |
|
![]() |
![]() |
![]() |
|
![]() |
![]() |
||||||||||||||||||||||||||||||||||||
| Sponsor: | University of Delaware |
|---|---|
| Information provided by: | University of Delaware |
| ClinicalTrials.gov Identifier: | NCT00843453 |
Purpose
This study was designed to determine whether elderly residents of long term care facilitated who had been taking proton pump inhibitors (PPI) for more than 12 months were more likely to have vitamin B12 deficiency than residents not taking PPI, and whether cyanocobalamin nasal spray improved these subjects' vitamin B12 status.
| Condition | Intervention |
|---|---|
|
Vitamin B12 Deficiency |
Other: blood collection Drug: treatment (cyanocobalamin nasal spray) |
| Study Type: | Interventional |
| Study Design: | Prevention, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment |
| Official Title: | Long-term Use of Proton Pump Inhibitors May Cause Vitamin B12 Deficiency in the Institutionalized Elderly |
| Enrollment: | 36 |
| Study Start Date: | November 2006 |
| Study Completion Date: | April 2008 |
| Primary Completion Date: | January 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
1
Comparison of serum vitamin and B12 concentrations of PPI and non-PPI groups
|
Other: blood collection
blood collection
|
|
2: Experimental
Comparison of baseline and end of treatment serum vitamin B12 and MMA concentrations.
|
Drug: treatment (cyanocobalamin nasal spray)
cyanocobalamin nasal spray -- 500 mcg q week for eight weeks
|
Subjects had serum creatinine <1.8 mg/dL, no diagnosis of severe megaloblastic or pernicious anemia, and had not been taking vitamin B12 supplements. At baseline, serum vitamin B12 and methylmalonic acid (MMA) concentrations of 34 subjects from the PPI group were compared with those of the non-PPI group. The PPI group (n=13) was treated with cyanocobalamin nasal spray for eight weeks, and post-treatment vitamin B12 and MMA concentrations were compared with baseline concentrations.
Eligibility| Ages Eligible for Study: | 60 Years to 89 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| United States, Maryland | |
| Stella Maris Nursing Home | |
| Timonium, Maryland, United States, 21093 | |
| Long View Nursing Home | |
| Manchester, Maryland, United States, 21102 | |
| Principal Investigator: | Nancy R Rozgony, RD< LD | University of Delaware |
| Principal Investigator: | Chengshun R Fang, Ph.D. | University of Delaware |
More Information
| Responsible Party: | University of Delaware ( Nancy R. Rozgony, MS, RD,LD ) |
| Study ID Numbers: | HS08-165 |
| Study First Received: | February 12, 2009 |
| Last Updated: | July 21, 2009 |
| ClinicalTrials.gov Identifier: | NCT00843453 History of Changes |
| Health Authority: | United States: Institutional Review Board |
|
vitamin B12 deficiency cyanocobalamin deficiency proton pump inhibitors omeprazole |
|
Vitamin B Complex Molecular Mechanisms of Pharmacological Action Vitamin B Deficiency Hematinics Avitaminosis Growth Substances Hematologic Agents Physiological Effects of Drugs Hydroxocobalamin Vitamin B 12 Deficiency |
Vitamin B 12 Enzyme Inhibitors Pharmacologic Actions Malnutrition Proton Pump Inhibitors Therapeutic Uses Vitamins Nutrition Disorders Micronutrients Deficiency Diseases |