- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT00609895
The Incidence of Hypoglycemia in Insulin Glargine-Treated Subjects With Diabetes Mellitus Upon Switching Between Bedtime and Morning Dosing
26. mars 2008 oppdatert av: Sanofi
To compare the percentage of subjects with a glucose measurement < than or = to 56 mg/dL at any point of the 8-point glucose profiles during 3 consecutive days before vs. 3 consecutive days after switching insulin glargine dosing time from bedtime to morning and vs. 3 consecutive days after switching back to bedtime dosing of insulin glargine.
Studieoversikt
Studietype
Intervensjonell
Registrering (Faktiske)
22
Fase
- Fase 4
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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Monterrey, Mexico
- Sanofi-Aventis
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Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
6 år til 75 år (Barn, Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria:
- Type 1 or type 2 diabetes mellitus diagnosis for at least 1 year Administration of insulin glargine for at least 2 months prior to screening; subjects must be on a stable dose of insulin glargine, + or - 15%, for at least 1 week prior to screening, given once daily at bedtime, and the dose must remain unchanged (+ or - 15%) during the screening period.
- If subjects are taking a short-acting insulin (e.g., regular human insulin, insulin lispro, or insulin aspart) or oral antidiabetic agents (e.g., a sulfonylurea, metformin, an alpha-glucosidase inhibitor, a thiazolidinedione, or a metiglinide), the subject must have been receiving these medications for at least 2 months prior to screening.
- For subjects taking an oral antidiabetic agent, the dose must be unchanged for the 2 weeks (4 weeks for a thiazolidinedione) prior to screening and should not be expected to be changed from the screening visit (day 14) through the final visit (day 11). The dose of any short-acting insulin may be changed if medically indicated.
- Males or non-pregnant females between the ages of 6 and 75 years; women must be postmenopausal for more than 2 years, surgically sterile, or agree to use a reliable contraceptive measure for the duration of the study. Reliable contraceptive measures include the following: systemic contraceptive (oral, implant, injections), diaphragm with intravaginal spermicide, cervical cap, intrauterine device, or condom with spermicide.
- Ability and willingness to perform blood glucose profiles using a plasma glucose meter provided at home over 11 consecutive days.
- HbA1c < than or = to 8.5% at screening.
Exclusion Criteria:
- Use of any other intermediate- or long-acting insulin (e.g., NPH, Ultralenter, Lenter) within the last 2 months prior to screening.
- Likelihood of requiring treatment during the study period with drugs not permitted by the study protocol (e.g., systemic corticosteroids).
- History of hypoglycemia unawareness.
- Pregnancy (as determined by a serum pregnancy test at the screening visit).
- Breast-feeding.
- Treatment with any investigational drug in the 2 months prior to the screening visit.
- Clinically relevant cardiovascular, hepatic, neurologic, endocrine, or other major systemic disease making implementation of the protocol or interpretation of the study results difficult.
- History of drug or alcohol abuse.
- Impaired hepatic function, as shown by but not limited to serum glutamic-oxaloacetic transaminase (SGPT, also known as alanine transaminase [ALT]) or serum glutamic-pyruvic transaminase (SGOT, also known as aspartate transaminase [AST]) above 2x the upper limit of normal range (ULN) measured at the screening visit.
- Impaired renal function, as shown by, but not limited to serum creatinine > than or = to 1.5 mg/dL (133 micromol/L) [males] or > than or = to1.4 mg/dL (124 micromol/L) [females] measured at the screening visit. Mental condition rendering the subject unable to understand the nature, scope, and possible consequences of the study. Subject unlikely to comply with protocol, e.g., uncooperative attitude, inability to return for follow-up visits, and unlikelihood of completing the study.
- Subjects who work the night shift.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomisert
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
---|---|
Compare % of subjects with glucose > or = to 56 mg/dL at any point of 8-point glucose profiles during 3 consecutive days
Tidsramme: before vs. after switching dosing time from bedtime to morning and vs. after switching back to bedtime
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before vs. after switching dosing time from bedtime to morning and vs. after switching back to bedtime
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Sekundære resultatmål
Resultatmål |
Tidsramme |
---|---|
Compare % subjects with glucose measurements < or = to 72 mg/dL & < or = to 36 mg/dL at any point of the 8-point glucose profile during 3 consecutive days
Tidsramme: before vs. after switching dosing time from bedtime to morning and vs. after switching back to bedtime
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before vs. after switching dosing time from bedtime to morning and vs. after switching back to bedtime
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To compare the mean daily rate of hypoglycemia during 3 consecutive days
Tidsramme: before vs. after switching dosing time from bedtime to morning and vs. after switching back to bedtime
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before vs. after switching dosing time from bedtime to morning and vs. after switching back to bedtime
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To compare the changes from baseline in glucose values at each specific measurement time of the 8-point glucose profile during 3 consecutive days
Tidsramme: before vs. after switching dosing time from bedtime to morning and vs. after switching back to bedtime
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before vs. after switching dosing time from bedtime to morning and vs. after switching back to bedtime
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To compare the incidence of symptomatic hypoglycemia
Tidsramme: at any time during 3 consecutive days before vs. after switching dosing time from bedtime to morning and vs. after switching back to bedtime
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at any time during 3 consecutive days before vs. after switching dosing time from bedtime to morning and vs. after switching back to bedtime
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To evaluate overall safety and tolerability based on adverse event reporting, laboratory tests, and clinical examinations
Tidsramme: at any time during the study
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at any time during the study
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Etterforskere
- Studieleder: Judith Diaz, Sanofi
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. januar 2004
Studiet fullført (Faktiske)
1. august 2004
Datoer for studieregistrering
Først innsendt
24. januar 2008
Først innsendt som oppfylte QC-kriteriene
6. februar 2008
Først lagt ut (Anslag)
7. februar 2008
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
28. mars 2008
Siste oppdatering sendt inn som oppfylte QC-kriteriene
26. mars 2008
Sist bekreftet
1. mars 2008
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- HOE901_4038
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .
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