TrialReader


To Evaluate the Effect on Post-prandial Glycemia Safety, and Tolerability of Viaject 7 vs. Lispro Insulin During Subcutaneous Insulin Pump Therapy

NCT01110746 — Phase 3, Completed, 20 participants, Biodel

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

A Double-blind Study of the Effect on Post-prandial Glycemia Safety, and Tolerability of Viaject 7 vs. Lispro Insulin During Subcutaneous Insulin Pump Therapy

RegistryNCT01110746
StatusCompleted
PhasePhase 3
Study typeInterventional; randomized, crossover, masking: double, treatment
Enrollment20 (Actual)
SponsorBiodel (Industry)
ConditionsType 1 Diabetes Mellitus
InterventionsViaject 7, LISPRO (Drug)
Datesstart 2010-02-01, primary completion 2010-06-01, completion 2010-06-01, first posted 2010-04-27, last updated 2015-08-03
Locations1 site in United States

Related Papers Related Patents Related Grants Related Experts
AI Assistant Save
All trials for Type 1 Diabetes Mellitus All trials of Viaject 7 All trials of LISPRO

-Summary

The purpose of this study is to evaluate the Effect on Post-prandial Glycemia Safety, and Tolerability of Viaject 7 vs. Lispro Insulin during SC Insulin Pump Therapy.

Expand all sections  ·  Collapse all

+Arms and interventions

ArmTypeInterventionsDescription
Formulation AExperimentalDrug: Viaject 7Single Injection
Formulation BExperimentalDrug: LISPROSingle Injection
  • Viaject 7 (Drug): 100IU/mL administered subcutaneously
  • LISPRO (Drug): 100IU/mL administered subcutaneously

+Outcome measures

Primary outcomes

  • 3 hour incremental area under the glucose curve after a standardized high glycemic index meal. [3 hours]

Secondary outcomes

  • Draize scores at insulin infusion site at 24 hour and 72 hour follow-up visits, frequency of discomfort with insulin infusion, and severity of discomfort with insulin infusion (ratings of mild, moderate, or severe). [72 hours]

+Eligibility

Sex: All, ages: 18 Years to 75 Years

Inclusion Criteria:

1. Males or females diagnosed with type 1 diabetes mellitus for at least 6 months
2. Current usage of subcutaneous insulin pump treatment with one of the following pumps:

   * Medtronic Paradigm®
   * Animas®
   * OmniPod®
   * ACCU-CHEK Spirit®
3. Age 18-75 years
4. HbA1c of 6.0 - 9.0% at screening visit.
5. Willingness to attend 9 clinic visits.

Exclusion Criteria:

1. Pregnancy or Lactation
2. Renal insufficiency (serum creatinine of 2.0 mg/dL or greater).
3. Anemia
4. Congestive heart failure.
5. Visual impairment preventing reading of glucose meter values or the ability to use an insulin pump or continuous glucose monitoring device.
6. Active coronary artery disease or heart procedure within the past 4 months.
7. Active foot ulceration.
8. Severe peripheral arterial disease.
9. Stroke within the past 6 months.
10. Active alcohol abuse, substance abuse, or severe mental illness.
11. Active cancer, except basal cell or squamous cell skin cancers.
12. Major surgical operation within 30 days prior to screening.
13. Seizure disorder (epilepsy).
14. Any concurrent illness, other than diabetes, that is not controlled by a stable therapeutic regimen.
15. Currently use of corticosteroids.
16. History of major non-compliance.
17. Use of an investigational drug within 30 days prior to screening.
18. Bleeding disorder, treatment with warfarin, or low platelet count.
19. Any insulin allergy
20. Current complaints of major infusion site problems with commercially- available insulin preparations, such as frequent occurrence of infections, marked swelling or marked erythema.
21. History of gastroparesis.

+Locations (1)

FacilityCityCountryStatus
Oregon Health and Science University/Legacy Health SystemPortland, OregonUnited States

My Notes