Administrative Claims Analysis of Metanx® in Diabetic Peripheral Neuropathy

This study has been completed.
Sponsor:
Collaborator:
HealthCore, Inc.
Information provided by (Responsible Party):
Pamlab, Inc. ( Pamlab, L.L.C. )
ClinicalTrials.gov Identifier:
NCT01247558
First received: November 17, 2010
Last updated: July 23, 2012
Last verified: July 2012

November 17, 2010
July 23, 2012
November 2010
September 2011   (final data collection date for primary outcome measure)
All-Cause Health Plan Costs [ Time Frame: 12 months post-index period ] [ Designated as safety issue: No ]
Total healthcare utilization and costs for patients treated with Metanx® will be compared to total healthcare utilization and costs for control patients who did not receive Metanx®. Cost data will be presented as Mean (SD) and median.
Same as current
Complete list of historical versions of study NCT01247558 on ClinicalTrials.gov Archive Site
  • Disease-Attributable Resoure Use and Cost [ Time Frame: 12 month post-index period ] [ Designated as safety issue: No ]
    Disease attributable resource use and costs will be defined as medical claims associated with ICD-9 codes for disease(s) of interest. Total attributable resource use (units) and cost (allowed or paid), if available, will include: pharmacy (medication related to disease of interest); laboratory tests (all claims); office-based encounters and costs; emergency room visits and cost; other outpatient facility (e.g. clinic, home health); in-patient hospitalization; and durable medical equipment.
  • Demographics of Patients Taking Metanx® [ Time Frame: >120 continuous days Metanx® therapy ] [ Designated as safety issue: No ]
    Statistical data including age (at index date); gender; comorbidities; prior and concomitant medications; and Metanx® utilization (e.g. dispensing quantity, number of fills, compliance, and persistency) will be collected to provide a descriptive analysis of the typical Metanx® patient characteristics.
Same as current
Not Provided
Not Provided
 
Administrative Claims Analysis of Metanx® in Diabetic Peripheral Neuropathy
Administrative Claims Analysis of Metanx® in Diabetic Peripheral Neuropathy

This study will be an observational cohort study utilizing administrative claims data with 100 patients randomly selected taking Metanx® meeting the inclusion and exclusion criteria and 400 propensity score matched patients meeting the same criteria to serve as a control cohort for analyses. This data includes medical, and pharmacy claims from the HealthCore Integrated Research Database for claims submitted during the time period of 01/01/2002 through 06/30/2007.

The control patients will be matched at a ratio of 4:1 with the Metanx® patients. Covariates used to select the propensity matched patients will include: age; gender; health plan type and region; DCI score; presence/absence of nephropathy; ischemic heart disease; cerebrovascular disease; neoplasm; insulin use; and all-cause health plan costs in the 6-mont pre-index period.

Claims information about patients selected for the study will be followed longitudinally to the end of data availability. This data stream will be used to determine treatment patterns for Metanx®, healthcare resource utilization, and cost.

Observational
Observational Model: Cohort
Time Perspective: Retrospective
Not Provided
Not Provided
Probability Sample

Patients with Diabetes and Peripheral Neuropathy or Peripheral Circulatory Disorder with Lower Limb Ulceration Who Have Been Treated with Metanx® or Not Treated with Metanx®.

Patients selected for the study will be identified from a review of available medical and pharmacy data during the period from 01/01/2003 to 06/30/2006. The date of the first pharmacy claim of interest within the intake period will be defined as the index date.

Diabetic Peripheral Neuropathy (DPN)
  • Other: Metanx® (a medical food)
    Patient cohort compliant on Metanx® BID therapy for >120 days
  • Other: Not treated with Metanx®
    Non-treated comparative cohort
  • Test Cohort
    100 randomized subjects administered Metanx®
    Intervention: Other: Metanx® (a medical food)
  • Control Cohort
    400 subjects with diabetes mellitus meeting the same inclusion and exclusion criteria as the test cohort who have not been treated with Metanx®.
    Intervention: Other: Not treated with Metanx®
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
500
September 2011
September 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Patients must have pharmacy claims for >120 continuous days of Metanx®. This will be defined as at least a 90-day supply dispensed within the first 120 days post-index. The first pharmacy claim for Metanx® will be the index date.
  • Patients must have a diagnosis of diabetes prior to or including the index date.
  • Patients must have a diagnosis of a peripheral neurological or a peripheral circulation disorder.
  • Patients must have a diagnosis of lower limb ulcer.

Exclusion Criteria:

  • Patients will be excluded if they have <18 months of eligibility defined as a minimum of 6 months pre and 12 months post-index eligibility.
  • Patients will be excluded if they have taken other L-methylfolate containing products (Deplin®, Cerefolin®, Cerefolin NAC®,Neevo®) or other prescription folic acid combination products with >1mg folic acid.
Both
25 Years to 80 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01247558
M-006
No
Pamlab, Inc. ( Pamlab, L.L.C. )
Pamlab, L.L.C.
HealthCore, Inc.
Study Director: Ron Wade, RPh, MS HealthCore, Inc.
Pamlab, Inc.
July 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP