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CompletedNCT01299012Updated Feb 9, 2017

Liraglutide as Additional Treatment in Patients With Type 1 Diabetes Mellitus

An observational study in Type 1 Diabetes Mellitus, sponsored by University at Buffalo. Completed. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2017-02-09.

Sponsored by University at Buffalo · Observational

Study type
Observational
Model
Other
Time perspective
Retrospective
Enrollment
30
Ages
18 Years to 65 Years
Sex
All
01

Study summary

Evaluating the use of Liraglutide in patients with Type 1 Diabetes.

Read the detailed description

This investigation will be a retrospective chart review of in type 1 diabetics who have been treated with liraglutide. The study will be conducted at Diabetes-Endocrinology Center of WNY at Millard Fillmore Hospital, affiliated to the State University of New York at Buffalo.

Study Population: 40 patients with type 1 diabetes on treatment with either continuous subcutaneous insulin infusion (CSII; also known as insulin pump) or multiple (four or more) injections of insulin per day on continuous glucose monitoring system (CGMS) will be included in the study. These patients with type 1 diabetes have been treated with liraglutide in addition to insulin. The investigators would retrospectively review their charts to evaluate decreases in fasting, postprandial and the overall mean glucose concentrations.

The investigators will compare the mean fasting, the mean weekly glucose and the standard deviation of weekly blood glucose concentrations as recorded by continuous glucose monitoring prior to and following one week and 12 weeks of treatment with liraglutide daily. In addition, the investigators will compare the time spent at glucose concentrations >150 and 200mg/dl and \<70 and \<40 mg/dl. HbA1c levels before and after 12 weeks of treatment with liraglutide daily will be compared.

02

Conditions studied

  • Type 1 Diabetes Mellitus
03

In context

Diabetes Mellitus

10,923 studies on the registry are indexed under Diabetes Mellitus; 1,318 are open to participants now.

This study's enrollment of 30 is below the median of 233 across 2,218 observational studies indexed under Diabetes Mellitus.

Browse Diabetes Mellitus studies →

Lead sponsor

University at Buffalo is the lead sponsor of 73 studies on the registry; none are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 5 (83%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Type 1 Diabetes Mellitus

Inclusion criteria

  • Type 1 Diabetes Mellitus

Exclusion criteria

Exclusion Criteria:

  • Type 2 Diabetes Mellitus
05

Study design

Observational model
Other
Time perspective
Retrospective
Enrollment
30 participants (actual)

Interventions

  • DrugLiraglutide

    Liraglutide s/c 0.6mg once daily.

    Also known as: Victoza

06

What researchers measure

Primary outcomes

  1. Improved Blood Glucose comtrol in Type 1 Diabetes Patients with Liraglutide

    Time frame: 20 weeks

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 9, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01299012
Lead sponsor
University at Buffalo
Responsible party
Paresh Dandona (MD, Kaleida Health) — Principal investigator
First posted
Feb 18, 2011
Start date
Oct 2010
Primary completion
Feb 2013
Completion
Jun 2013
Last update
Feb 9, 2017

Study contacts

Paresh Dandona
principal investigator · University at Buffalo

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2017. You cannot join it, but the record below documents what was studied.

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