- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02591628
Treatment of Hypertension In Adults With ThiaZIDES: Pragmatic Trial Pilot Study (ThiaZIDES)
10. oktober 2017 opdateret af: HealthPartners Institute
This proposed pilot study will test methods and feasibility for a large pragmatic clinical trial comparing two inexpensive, first-line drugs for treating high blood pressure to determine if one is superior in preventing serious cardiovascular events and death.
It will develop and test novel approaches to conducting trials that will be faster, less expensive, and more realistic by being embedded in a typical practice setting and using advanced health information technology.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
For several decades, U.S. hypertension treatment guidelines have recommended a low-dose diuretic such as hydrochlorothiazide (HCTZ) or chlorthalidone (CTD) as initial monotherapy in a stepped-care approach or as part of an initial two-drug combination.
In numerous large clinical trials, CTD-based regimens have significantly reduced rates of cardiovascular events such as stroke, heart failure, and cardiovascular mortality compared with placebo, usual care, or active comparators.
In contrast, few outcome studies have compared HCTZ-based regimens with other treatments, and they have generally found HCTZ to be less effective than non-thiazide comparators in preventing cardiovascular events.
The two drugs have never been compared directly in a large trial.
Despite the empirical evidence favoring CTD, HCTZ is much more widely used in clinical practice.
The proposed R34 is a pilot study conducted in two large integrated health systems to test methods and feasibility for an eventual pragmatic randomized trial comparing the effectiveness of HCTZ and CTD for preventing cardiovascular events and mortality.
Using a cluster-randomized design, investigators will allocate 40 primary care physicians and their adult hypertensive patients who currently use HCTZ (N=2,000) to either convert HCTZ users to CTD (intervention group) or to continue HCTZ (usual care group).
The pilot study and planned full-scale trial will use existing health care infrastructure and electronic health records to identify eligible study subjects, distribute study medication, and collect operational and outcomes data.
For this pilot study, Aim 1 will document that the intervention is delivered as intended.
Aim 2 will compare safety in intervention and usual care patients.
Aim 3 will refine the pilot study design and identify critical factors for intervention success using a mixed-methods approach.
Aim 4 will refine estimates of sample size.
Finally, Aim 5 will determine the costs of ascertaining outcomes and estimate per-participant costs for the full-scale trial.
The pilot study will produce data that are necessary and sufficient to inform the planning of a full-scale trial comparing CTD and CTZ and will advance the development of methods for pragmatic trials.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
2027
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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Minnesota
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Bloomington, Minnesota, Forenede Stater, 55105
- HealthPartners Institute for Education and Research
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Oregon
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Portland, Oregon, Forenede Stater, 97227
- Kaiser Permanente Center for Health Research
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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 og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Adults 18 years and older
- Hypertension diagnosis (ICD-9 401.x)
- Current prescription for hydrochlorothiazide (HCTZ), 12.5-50 mg/day as a single-agent (not part of a fixed-dose combination drug)
- No history of intolerance to chlorthalidone (CTD)
- No known low levels of sodium (<135 mEg/L (milliequivalents per liter)) or potassium (<3.5 mEg/L)
- English speaking
Exclusion Criteria:
- Physician deems patient inappropriate for switching HCTZ to CTD
- Patient refuses the switch prior to intervention
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: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Aktiv komparator: Intervention
Intervention is HCTZ prescription conversion to chlorthalidone.
Intervention patients are defined as patients of physicians randomized to "intervention."
All these patients will have their current prescription of hydrochlorothiazide (HCTZ) switched to an equipotent dose of Chlorthalidone.
These patients can choose to decline this intervention, and will be followed for 9 months with no other intervention to observe primary and secondary outcomes.
|
The intervention is simply a prescription conversion and the main outcome is whether or not patients accept the conversion and treatment with chlorthalidone.
|
|
Ingen indgriben: Usual Care
Usual care patients are defined as patients of physicians randomized to "usual care."
All these patients will keep their current prescription for HCTZ and work with their physician like normal.
These patients will be followed for 9 months with no intervention to compare primary and secondary outcomes to the intervention group.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Conversion to chlorthalidone, number of patients with primary fills
Tidsramme: 3 months
|
We will observe pharmacy claims to assess whether intervention patients filled their first prescription for chlorthalidone (primary adherence)
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3 months
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Conversion to chlorthalidone, number of participants with secondary fills
Tidsramme: 9 months
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We will observe pharmacy claims to assess whether intervention patients who filled their first chlorthalidone prescription also filled their subsequent prescription (secondary adherence)
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9 months
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Blood pressure
Tidsramme: 9 months
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Systolic and diastolic blood pressure measures, as documented in electronic health record
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9 months
|
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Hypertension drugs
Tidsramme: 9 months
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Use of anti-hypertensive drugs in addition to hydrochlorothiazide or chlorthalidone, as documented in pharmaceutical claims
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9 months
|
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Electrolyte levels
Tidsramme: 9 months
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Sodium and potassium levels, as documented in electronic health record
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9 months
|
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Renal function
Tidsramme: 9 months
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Kidney function lab values (including epidermal growth factor receptor (eGFR) and creatinine), as documented in electronic health record
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9 months
|
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Safety outcomes
Tidsramme: 9 months
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Hypotension with fainting (over-treatment), hypertensive crisis (under-treatment) and other clinical outcomes related to safety of hypertension treatment
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9 months
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Karen L Margolis, MD, MPH, HealthPartners Institute
- Ledende efterforsker: Stephen P Fortmann, MD, Kaiser Permanente
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
1. august 2015
Primær færdiggørelse (Faktiske)
1. juli 2017
Studieafslutning (Faktiske)
1. juli 2017
Datoer for studieregistrering
Først indsendt
25. september 2015
Først indsendt, der opfyldte QC-kriterier
28. oktober 2015
Først opslået (Skøn)
29. oktober 2015
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
11. oktober 2017
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
10. oktober 2017
Sidst verificeret
1. januar 2017
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- R34HL119790 (U.S. NIH-bevilling/kontrakt)
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 .
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