LivingGLP1
Study S001233

Changes in Bone Turnover With Exposure to a GLP-1 Receptor Agonist (UAB Core Center for Basic Skeletal Research)

Registration

Registration
NCT01381926
Acronym
CMBD
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE4
Masking
DOUBLE
Status
TERMINATED
Enrollment
14
Start
2011-02
Primary completion
2015-08
Lead sponsor
University of Alabama at Birmingham
Conditions
Type 2 Diabetes Mellitus; Bone Remodeling
Interventions
DRUG:exenatide; DRUG:Saline
Results posted
TRUE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • Determine Changes in Bone Resorption Markers During the Treatment With a GLP-1 Receptor Agonist (Exenatide) Compared to Placebo in Patients With T2DM. [Baseline to 20 weeks]
  • Determine Changes in Bone Turnover Markers by Serum N-Telo Peptide During the Treatment With a GLP-1 Receptor Agonist (Exenatide) Compared to Placebo in Patients With T2DM. [Baseline to 20 weeks]
  • Determine Changes in Bone Turnover Markers by Tartrate-Resistant Acid Phosphatase 5b (TRACP5b) During the Treatment With a GLP-1 Receptor Agonist (Exenatide) Compared to Placebo in Patients With T2DM. [Baseline to 20 weeks]

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