Use of Sitagliptin to Decrease Microalbuminuria
Clinical Effect of Dipeptidyl Peptidase-4 (DPP-4) Inhibitors in Urinary Albumin to Creatinine Ratio in Patients With Overt Kidney Disease
The people being asked to participate in this study have type 2 diabetes and abnormal levels of protein in their urine. This indicates that they are starting to develop diabetic kidney disease. The standard treatment for this is the use of one of two blood pressure medicines, either an angiotensin converting enzyme (ACE) inhibitor or angiotensin receptor blocker (ARB). However, these medicines are not always completely effective in stopping/reversing the kidney disease. Some studies have previously suggested that another type of medicine, called sitagliptin, normal used to treat diabetes may also help prevent diabetic kidney disease from getting worse.
This study is being performed to test the effectiveness of sitagliptin as compared to a placebo, along with a stable dose of an ACE inhibitor or ARB, to determine whether or not it will reduce protein levels in their urine. Protein levels in the urine are a marker of the severity of kidney disease.
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
Studietyp
Inskrivning (Faktisk)
Fas
- Fas 4
Kontakter och platser
Studieorter
-
-
Missouri
-
Columbia, Missouri, Förenta staterna, 65212
- University of Missouri-Columbia: Diabetes Center
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria:
- Albumin/creatinine ratio between 30-299 mg/dl.
- type 2 diabetes mellitus (T2DM) with hemoglobin A1c between 7 and 9%.
- Stable BP control of less than 145/90 on treatment with ACE or ARB for more than three months prior and during the trial.
- Glomerular filtration rate (GFR) of 60 mL/min/1.73m2 or more.
- Age between 18-75 years old.
- For women: at least two years postmenopausal, surgically sterile, or using an acceptable contraceptive regiment to include oral contraceptive pill (OCP), intrauterine device (IUD), double barrier, depo-provera, or subcutaneous progestin implant and negative urine pregnancy test at trial start.
Exclusion Criteria:
- Pregnancy.
- GFR less than 60 mL/min/73m2.
- Have a history of malignancy other than basal cell or squamous cell skin cancer and have not yet been treated, are currently being treated, or were diagnosed less than 5 years prior to Visit 1.
- Advanced liver disease.
- Subjects cannot be on DPP-4 inhibitor or glycolipoprotein (GLP-1) agonist for at least 4 months before the study start.
- Psychiatric condition that would prevent subject from following directions. Per PI discretion.
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Dubbel
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Aktiv komparator: Sitagliptin
100 mg/day for 3 months
|
Sitagliptin 100 mg/day for 3 months
Andra namn:
|
|
Placebo-jämförare: Placebo
1 pill/day for 3 months
|
Placebo 1 pill/day for 3 months
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Change in Microalbuminuria Level
Tidsram: Six months
|
Decrease in microalbuminuria level
|
Six months
|
Samarbetspartners och utredare
Sponsor
Utredare
- Huvudutredare: Guido Lastra Gonzalez, MD, University of Missouri-Columbia
Studieavstämningsdatum
Studera stora datum
Studiestart
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
- Störningar i glukosmetabolism
- Metaboliska sjukdomar
- Sjukdomar i det endokrina systemet
- Diabetes mellitus
- Diabetes mellitus, typ 2
- Hypoglykemiska medel
- Läkemedels fysiologiska effekter
- Molekylära mekanismer för farmakologisk verkan
- Enzyminhibitorer
- Hormoner
- Hormoner, hormonsubstitut och hormonantagonister
- Proteashämmare
- Inkretiner
- Dipeptidyl-Peptidas IV-hämmare
- Sitagliptinfosfat
Andra studie-ID-nummer
- 1207397
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
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