GIP: Glucose-dependent Insulinotropic Peptide
Completed · Phase 1
Conditions studied: Type 2 Diabetes
In brief
The purpose of this study is to test the safety of glucose-dependent insulinotropic peptide (GIP)/GIP Analog on people with Type 2 Diabetes.
Key facts
- Study ID
- NCT00239707
- Run by
- National Institute on Aging (NIA)
- People needed
- 41
- Starts
- 2003-02-01
- Expected to finish
- 2006-12-01
- Last updated by the study team
- 2013-11-28
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 18 years of age and older
- Healthy Type 2 Diabetics
- Agree to stay off glucosidases for 3 days prior to infusion visits (Examples: Precose, Glyset)
- Agree to stay off Sulfonylureas 5 days prior to infusion visits (Examples: Glucotrol, Amaryl, glyburide, metformin
- Able to ingest 1000 mg Tylenol on study visits
- Able to consume study breakfast consisting of scrambled egg, white toast with margarine, corn flakes, 2% milk, banana at each infusion visit
- Female participants must have Hct > 36
- Male participant must have Hct > 38
- No kidney or liver disease per history and evidenced by blood and urine tests
- Physical Exam and EKG that do not contraindicate patient to be in the study
You may not qualify if…
- Taking the following medications: Insulin, or Thiazolidinediones, i.e. Avandia, Actos
- Pregnancy
- Steroid use within the past 3 months
- Recent infection, fever or chills
Where it is running
- National Institute on Aging, Clinical Research Branch — Baltimore, Maryland, United States
Full record on ClinicalTrials.gov
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