- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02338232
Undersøgelse af telmisartan til forebyggelse af akut GVHD postallogen hæmatopoietisk stamcelletransplantation
24. februar 2023 opdateret af: Hackensack Meridian Health
Pilotundersøgelse af telmisartan (Micardis) til forebyggelse af akut graft vs. værtssygdom efter allogen hæmatopoietisk stamcelletransplantation
Dette er et enkelt-center, åbent, prospektivt studie af telmisartan til forebyggelse af akut GVHD hos ca. 60 forsøgspersoner, der gennemgår allogen HCT til behandling af en hæmatologisk malignitet.
Studieoversigt
Detaljeret beskrivelse
Dette er et enkelt-center, åbent, prospektivt studie af telmisartan til forebyggelse af akut GVHD hos ca. 60 forsøgspersoner, der gennemgår allogen HCT til behandling af en hæmatologisk malignitet.
Forsøgspersonerne vil modtage 160 mg Micardis-mærket telmisartan én gang dagligt, startende 2 dage før HCT (dag -2).
Når patienten er udskrevet efter HCT, vil behandlingen fortsætte til og med dag +98 efter HCT i i alt 101 dage.
Efter behandlingsophør på eller før dag +98 post-HCT, vil forsøgspersoner blive fulgt i op til 6 måneder for primære og sekundære endepunkter.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
32
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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New Jersey
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Hackensack, New Jersey, Forenede Stater, 07601
- Hackensack University Medical Center
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år til 99 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inklusionskriterier:
Diagnose af:
- Akut myeloid eller lymfoid leukæmi i remission,
- myelodysplastisk syndrom,
- Kronisk lymfoid leukæmi,
- Non-Hodgkin lymfom,
- Hodgkin lymfom,
- Kronisk myeloid leukæmi i kronisk eller accelereret fase,
- Myeloproliferativ lidelse, eller
- Myelomatose
- Undergår allogen HSC-transplantation fra en relateret eller ikke-beslægtet donor matchede mindst 7 af 8 af HLA-A-, -B-, -C- og DR-lociene ("8/8" eller "7/8" match)
Undergår allogen HSC-transplantation efter et myeloablativt TBI-, busulfan- eller (ikke-myeloablativt) melphalan-baseret præ-transplantationskonditioneringsregime. Regimer til transplantation vil omfatte et af følgende midler givet i forbindelse med fludarabin eller cyclophosphamid:
- Busulfan 130 mg/m2 iv dagligt x 2 (reduceret intensitet) eller 4 dage
- TBI 150 cGy bid x 8 doser (1200 Gy)
- Melphalan 140 mg/m2. (Selvom melphalan ikke er et myeloablativt regime, resulterer det i klinisk signifikant mucositis, og patienter, der modtager denne medicin, vil være af betydelig interesse i analysen af disse data.)
- Mandlig eller kvindelig patient på 18 år eller ældre
- Karnofsky præstationsstatus > 70 % på tidspunktet for påbegyndelse af præ-transplantationskonditionering
- Transplantationsspecifik co-morbiditetsscore på <5 på tidspunktet for påbegyndelse af præ-transplantationskonditionering
- Patienter, der tager antihypertensiv medicin (inklusive telmisartan) er kvalificerede, men patienten skal afbryde behandlingen mindst 48 timer før første dosis af undersøgelsesmedicin
- I stand til at give informeret samtykke og have underskrevet formularen til informeret samtykke
Ekskluderingskriterier:
- Manglende evne til at give informeret samtykke
- Personer med kendt hjertesvigt, fremskreden nyreinsufficiens, der kræver nyreudskiftningsterapi, eller leversvigt, selvom disse patienter højst sandsynligt ikke ville være berettiget til HCT.
- Forsøgspersoner, der tager ACE-hæmmere, kaliumtilskud eller spironolacton (eller andre kaliumbesparende diuretika), som ikke kan ophøre med at bruge før påbegyndelse af undersøgelsesbehandling ELLER som har behov for en kost med højt kaliumindhold
- Patient ude af stand til at seponere aktuel hypertensionsmedicin af medicinske eller andre årsager i to dage før start med telmisartan
- Kronisk symptomatisk hypotension, volumenudtømning.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Eksperimentel: 160 mg Telmisartan
60 patienter vil modtage 160 Telmisartan (2 80 mg tabletter) i 101 dage
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Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
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Antal forsøgspersoner med grad 3 eller højere akut graft vs. værtssygdom (GVHD) hos patienter, der får allogen HCT.
Tidsramme: 100 dage efter transplantationen
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100 dage efter transplantationen
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Sekundære resultatmål
Resultatmål |
Tidsramme |
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Antal forsøgspersoner med grad III-IV hypotension i henhold til National Cancer Institutes fælles terminologi
Tidsramme: 180 dage efter transplantation
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180 dage efter transplantation
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
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Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
7. juli 2015
Primær færdiggørelse (Faktiske)
5. januar 2023
Studieafslutning (Faktiske)
5. januar 2023
Datoer for studieregistrering
Først indsendt
5. januar 2015
Først indsendt, der opfyldte QC-kriterier
9. januar 2015
Først opslået (Skøn)
14. januar 2015
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
28. februar 2023
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
24. februar 2023
Sidst verificeret
1. februar 2023
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- Pro5465
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