Kronisk lymfatisk leukæmi reagerer på dermal chelation
4. april 2018 opdateret af: Optimum Health, Natural Healthcare Center
Dermal chelation sænker antallet af hvide blodlegemer ved kronisk lymfatisk leukæmi
Formålet med dette kliniske forsøg er at identificere 50 deltagere med kronisk lymfatisk leukæmi (CLL) og følge deres totale antal hvide blodlegemer (WBC) og absolutte lymfocyttal efter at have udført dermal chelation og administreret ernæringsterapi
Studieoversigt
Status
Ukendt
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Formålet med dette kliniske forsøg er at bruge dermal chelation og hårvævsanalyse til at identificere 50 deltagere med CLL.
De samlede wbc-tal og absolutte lymfocyttal for disse deltagere vil blive fulgt efter serielle dermale chelationer og ernæringsterapi.
Undersøgelsestype
Interventionel
Tilmelding (Forventet)
50
Fase
- Ikke anvendelig
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 og ældre (VOKSEN, OLDER_ADULT)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inklusionskriterier:
- Klinisk diagnose af kronisk lymfatisk leukæmi og har en giftig tungmetalbelastning
- Giftig tungmetalbelastning
Ekskluderingskriterier:
- Gravid
- Pacemakerimplantater
- Organtransplanterede modtagere
- Psykotiske episoder eller epileptiske anfald
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: NA
- Interventionel model: SINGLE_GROUP
- Maskning: INGEN
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
EKSPERIMENTEL: Deltagere
Gruppe, der modtager dermal chelation og ernæringsterapi
|
Dermal chelation med Aqua DetoxTM system i en eller flere timer en eller flere gange om ugen.
Vitaminer og mineraler, der vil blive taget en eller flere gange om dagen.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Seriel totalt antal hvide blodlegemer
Tidsramme: op til 12 måneder
|
Totalt antal hvide blodlegemer taget med et regelmæssigt interval.
|
op til 12 måneder
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
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.
Generelle publikationer
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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 (FORVENTET)
1. december 2018
Primær færdiggørelse (FORVENTET)
1. marts 2019
Studieafslutning (FORVENTET)
1. marts 2019
Datoer for studieregistrering
Først indsendt
14. februar 2018
Først indsendt, der opfyldte QC-kriterier
4. april 2018
Først opslået (FAKTISKE)
12. april 2018
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (FAKTISKE)
12. april 2018
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
4. april 2018
Sidst verificeret
1. april 2018
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- DCCLL2018
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Kronisk lymfatisk leukæmi
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Jules Bordet InstituteMacopharma; Belgian Hematological SocietyRekrutteringRefractory Chronic Graft Versus Host Disease (cGVHD)Belgien
-
Bahria UniversityIslamabad Medical and Dental CollegeAktiv, ikke rekrutterendeAlveolær knogletab Associated Chronic PeriodontitisPakistan
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West China HospitalIkke rekrutterer endnuPTLD'er | CAEBV (Chronic Active Epstein-Barr Virus Infection) SyndromKina
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Beijing Friendship HospitalIkke rekrutterer endnuEBV | Hæmofagocytiske lymfohistiocytoser | CAEBV (Chronic Active Epstein-Barr Virus Infection) SyndromKina
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Novartis PharmaceuticalsLedigPrimær myelofibrose (PMF) | Polycytæmi Vera (PV) | Post polycytæmi myelofibrose (PPV MF) | Trombocytæmi myelofibrose (PET-MF) | Alvorlig/meget svær COVID-19 sygdom | Steroid Refractory Acute Graft Versus Host Disease (SR aGVHD) | Steroid Refractory Chronic Graft Versus Host Disease (SR cGVHD)
Kliniske forsøg med Dermal Chelation
-
Novartis PharmaceuticalsAfsluttetAplastisk anæmiDen Russiske Føderation
-
ApoPharmaAfsluttetDiabetisk fodsårForenede Stater
-
Semikal TechnologyAktiv, ikke rekrutterendePeriorbitale rynker | Korrektion af nasolabial fold | Volumenfejl i midtansigtet | Hudforyngelse | Marionette linjer | Ansigts aldring | Læbeforstørrelse og korrektion af periorale rytmer | Reduktion af ansigtsrynker og rytmerTyrkiet (Türkiye)
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Center of Implantology, Oral and Maxillofacial...Rekruttering
-
University of UtahAfsluttetBrystkræft | Rekonstruktiv kirurgiForenede Stater
-
Istituto Ortopedico RizzoliRekruttering
-
Aarhus University HospitalAfsluttet
-
Kylane LaboratoiresEurofins Dermscan PharmascanAfsluttetÆstetisk dermatologiSchweiz
-
University of Texas Southwestern Medical CenterAfsluttet
-
Faculty of Dental Medicine for GirlsAfsluttetSammenlignende undersøgelseEgypten