- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT00814177
Prothrombin Times Outside the Therapeutic Range in Otherwise Stable Patients (FORESPEAK-0)
Management of Prothrombin Times Outside the Therapeutic Range in Patients on Warfarin and With Otherwise Stable Levels
Warfarin is very effective for the prevention of blood clots (thrombosis). A test of coagulation, the prothrombin time (PT) is used to monitor the effect. The PT response to warfarin can fluctuate as a result of interactions with a large number of other drugs, food or herbal agents as well as for no apparent reason. Thus, frequent monitoring of the PT and dose adjustments according to the results are required. One third of our patients remain on the same maintenance dose over 6 months. However, also these patients sometimes have a PT result moderately outside the therapeutic range without any obvious explanation. Too short PTs may be due to missed dose(s) or more dark green vegetables in the diet. Too long PTs may be due to a course of antibiotic therapy or less dark green vegetables. Laboratory errors may also occur and can cause deviations in any direction. Most likely, unnoticed fluctuations in the PT occur as well between the time points of monitoring.
There are no guidelines on how to manage the treatment in this situation but there are some typical "behaviours".
Behavior A: Some physicians simply let the patient continue with the same dose. "It is extremely unlikely that the very temporary dose adjustment has any effect on the PT result 4 weeks later and this is a "cosmetic procedure"." Behavior B: Others recommend the patients to take ½ - 1 additional dose in case of short PT and to skip a dose or take half dose in case of long PT, and thereafter to continue with the usual dose. "The investigators need to quickly correct the temporary aberration in order to avoid thrombotic or bleeding complications the next few days.
This may seem like an issue of no importance. The investigators are however performing a series of studies to evaluate if these stable patients can be managed with blood tests less often than every 4 weeks. For that purpose it is important to know how often and why aberrant results occur, the implication and to what extent they can be ignored.
The investigators hypothesis is that in patients with very stable PT-results and unchanged dose for 3 months, should continue with exactly the same maintenance dose, even when the result unexpectedly is slightly above or below the therapeutic range. The investigators believe that most of these occasional PT-results outside the therapeutic range are due to laboratory errors, perhaps missed doses by the patient or temporary change in diet or medications.
Panoramica dello studio
Stato
Intervento / Trattamento
Descrizione dettagliata
Setting:
Thrombosis Service at HHS - General Hospital. This center monitors the warfarin treatment for 1300 patients in the region. These patient regularly go to a laboratory where they live. Test results (INR-results) are faxed to the Thrombosis Service, which calls the patient the same day to inform them of the results, how to continue dosing the warfarin and when to go for the following blood test.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Fase 2
Contatti e Sedi
Luoghi di studio
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Ontario
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Hamilton, Ontario, Canada, L8L 2X2
- Thrombosis Service, HHS-General Hospital
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Patients on long-term warfarin (for prophylaxis of arterial embolism in patients with atrial fibrillation or mechanical heart valve replacement, or secondary prophylaxis after VTE) with a target INR of 2.0-3.0 or 2.5-3.5,
- Anticoagulant therapy managed by the clinic (HHS - General Hospital) for at least 3 months prior to enrolment, and
- Maintenance dose of warfarin unchanged for the previous 3 months or longer.
- The INR result is outside the therapeutic range as follows:
For those with target 2.0-3.0: Either an INR of 1.5-1.9 or an INR of 3.1-4.4. For those with target 2.5-3.5: Either an INR of 1.5-2.4 or an INR of 3.6-4.4.
Exclusion Criteria:
- Age <18 years,
- Long-term (>1 week) change in any other medication
- Long-term (>1 week) change in diet, especially regarding green vegetables.
- Attending physician believes the patient is not suitable for the study (e.g. psychiatric disorder, history of non-compliance),
- Failure to obtain telephone consent.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: No change
Intervention Drug warfarin no change in the dose is performed
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No change: Continue without any change in spite of prothrombin time outside the therapeutic range.
Altri nomi:
Change: Increase one dose in case prothrombin time is below the therapeutic range; delete or reduce one dose in case prothrombin time is above the therapeutic range.
Altri nomi:
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Comparatore attivo: Change
Intervention Drug Warfarin One dose increased if subtherapeutic level; one dose deleted or reduced if supratherapeutic level
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No change: Continue without any change in spite of prothrombin time outside the therapeutic range.
Altri nomi:
Change: Increase one dose in case prothrombin time is below the therapeutic range; delete or reduce one dose in case prothrombin time is above the therapeutic range.
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Number of Patients With Prothrombin Time Results Within the Therapeutic Range After 2 Weeks
Lasso di tempo: 2 weeks
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The number of patients with "follow-up INRs" within the therapeutic range was compared for patients with a single dose skipped/reduced/added versus patients with no change of dose.
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2 weeks
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Collaboratori e investigatori
Pubblicazioni e link utili
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Ischemia
- Processi patologici
- Necrosi
- Ischemia miocardica
- Malattie cardiache
- Malattia cardiovascolare
- Malattie vascolari
- Disturbi cerebrovascolari
- Malattie del cervello
- Malattie del sistema nervoso centrale
- Malattie del sistema nervoso
- Embolia e Trombosi
- Aritmie, cardiache
- Ictus
- Infarto miocardico
- Infarto
- Ictus ischemico
- Fibrillazione atriale
- Tromboembolia
- Tromboembolia venosa
- Anticoagulanti
- Warfarin
Altri numeri di identificazione dello studio
- HRC060425
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
Prove cliniche su warfarin
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University Hospital, BrestCompletato
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Federal University of São PauloFundação de Amparo à Pesquisa do Estado de São PauloCompletatoFibrillazione atrialeBrasile
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University of PadovaCompletatoTrombosi venosa profondaItalia
-
Duke UniversityNational Heart, Lung, and Blood Institute (NHLBI); Duke Clinical Research InstituteTerminatoFibrosi Polmonare IdiopaticaStati Uniti
-
Azienda Ospedaliera Universitaria PoliclinicoCompletatoTrombosi venosa profondaItalia
-
National University Hospital, SingaporeSconosciutoIndicazioni per la terapia con WarfarinSingapore, Malaysia
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Asan Medical CenterNon ancora reclutamentoInsufficienza cardiaca avanzata | Complicanze emorragiche | Trattamento anticoagulante | Dispositivi di assistenza ventricolare sinistra | Complicanze tromboticheCorea, Repubblica di
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Aalborg University HospitalCompletato
-
Iverson Genetic Diagnostics, Inc.SospesoFibrillazione atriale | Embolia polmonare | TVP | Sostituzione protesica della valvola mitrale | Terapia anticoagulante | Chirurgia articolare multiplaStati Uniti
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University of KarachiAdvanced Education & Research Center; Karachi Institute of Heart DiseasesReclutamentoAneurisma dell'appendice atriale sinistra | Stenosi mitralicaPakistan