- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT01875991
Preference Between Two Autoinjectors in Patients With Rheumatoid Arthritis and Plaque Psoriasis Treated With Etanercept
An Open-label, Randomized, Crossover Study to Assess the Preference for Autoinjector A Versus Autoinjector B in Rheumatoid Arthritis and Plaque Psoriasis Subjects Treated With Etanercept
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
Studientyp
Einschreibung (Tatsächlich)
Phase
- Phase 4
Kontakte und Standorte
Studienorte
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British Columbia
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Victoria, British Columbia, Kanada, V8V 3P9
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Newfoundland and Labrador
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St. John's, Newfoundland and Labrador, Kanada, A1C 5B8
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Ontario
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Barrie, Ontario, Kanada, L4M 7G1
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Burlington, Ontario, Kanada, L7R 1E2
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Courtice, Ontario, Kanada, L1E 3C3
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Hamilton, Ontario, Kanada, L8N 1Y2
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Mississauga, Ontario, Kanada, L5M 2V8
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Oakville, Ontario, Kanada, L6J 7W5
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Peterborough, Ontario, Kanada, K9J 1Z2
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Alabama
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Huntsville, Alabama, Vereinigte Staaten, 35801
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Tuscaloosa, Alabama, Vereinigte Staaten, 35406
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Arizona
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Glendale, Arizona, Vereinigte Staaten, 85304
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Scottsdale, Arizona, Vereinigte Staaten, 85258
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Arkansas
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Hot Springs, Arkansas, Vereinigte Staaten, 71913
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California
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San Diego, California, Vereinigte Staaten, 92108
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San Ramon, California, Vereinigte Staaten, 94583
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Santa Maria, California, Vereinigte Staaten, 93454-6945
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Tustin, California, Vereinigte Staaten, 92780
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Colorado
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Denver, Colorado, Vereinigte Staaten, 80230
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Florida
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Dunedin, Florida, Vereinigte Staaten, 34698
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Tampa, Florida, Vereinigte Staaten, 33614
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Kansas
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Overland Park, Kansas, Vereinigte Staaten, 66215
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Kentucky
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Louisville, Kentucky, Vereinigte Staaten, 40217
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Maryland
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Frederick, Maryland, Vereinigte Staaten, 21702
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Michigan
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Lansing, Michigan, Vereinigte Staaten, 48910
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Nebraska
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Lincoln, Nebraska, Vereinigte Staaten, 68516
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New York
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Orchard Park, New York, Vereinigte Staaten, 14127
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North Dakota
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Bismarck, North Dakota, Vereinigte Staaten, 58502
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Ohio
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Dayton, Ohio, Vereinigte Staaten, 45417
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Oklahoma
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Oklahoma City, Oklahoma, Vereinigte Staaten, 73103
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Pennsylvania
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Duncansville, Pennsylvania, Vereinigte Staaten, 16635
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Wyomissing, Pennsylvania, Vereinigte Staaten, 19610
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South Carolina
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Charleston, South Carolina, Vereinigte Staaten, 29414
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Tennessee
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Hixson, Tennessee, Vereinigte Staaten, 37343
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Texas
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Austin, Texas, Vereinigte Staaten, 78731
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Dallas, Texas, Vereinigte Staaten, 75231
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West Virginia
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Clarksburg, West Virginia, Vereinigte Staaten, 26301
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria: Diagnosis of moderate to severe Rheumatoid Arthritis (RA) or moderate to severe Plaque Psoriasis (PsO) and a candidate for treatment with etanercept in the opinion of the investigator in addition to the caring physician's intent to initiate treatment with etanercept. - Naive to etanercept. - Naive to other autoinjector pens or prefilled syringes for Tumor Necrosis Factor (TNF)-inhibitor therapy or other subcutaneous biologics for RA. - Willing to self-inject per investigator judgement at screening and capable of self-injection using the autoinjector A or B as documented at baseline by the investigator. - Able to read and write in English. -
Exclusion Criteria: Latex allergy. - Subject has an active infection (including chronic or localized infections) for which anti-infectives were indicated within 4 weeks prior to first dose of etanercept. - Subject had prosthetic joint infection within 5 years of screening or native joint infection within 1 year of screening.
- Other criteria may apply.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Crossover-Aufgabe
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
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Experimental: Autoinjector A
Participants self-injected 50 mg etanercept once a week (RA) or twice a week (PsO) using Autoinjector A for 4 weeks.
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Autoinjector A is a hand-held, reusable, electromechanical device used with a single-use disposable cassette preassembled with an etanercept 50-mg prefilled syringe.
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Experimental: Autoinjector B
Participants self-injected 50 mg etanercept once a week (RA) or twice a week (PsO) using Autoinjector B for 4 weeks.
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Autoinjector B is a single-use, spring-loaded, self-contained autoinjector preassembled with an etanercept 50-mg prefilled syringe.
Andere Namen:
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
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Percentage of Participants With a Preference for Autoinjector A Versus Autoinjector B
Zeitfenster: Week 8
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Preference for autoinjector A versus autoinjector B was assessed by Question 1 of the Subject Preference Questionnaire administered after the completion of the 2 treatment periods at Week 8. Participants answered the question "Which autoinjector do you prefer overall?"
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Week 8
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
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Change From Baseline in Needle Apprehension at Week 4
Zeitfenster: Baseline and Week 4
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Participants' needle apprehension was assessed using the Subject's Perception of Self-Injecting Questionnaire.
Participants answered the question "Overall how nervous are you about the needle when you think about giving yourself etanercept using the autoinjector" using a scale from 1 (extremely nervous) to 5 (not at all nervous).
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Baseline and Week 4
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Ease of Use
Zeitfenster: At the end of each treatment period; Week 4 and Week 8
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Ease of use was assessed based on responses to questions 1 to 6 of the Subject's Experience with the Autoinjector Questionnaire: 1.
How easy was it to learn how to use the autoinjector?
2. How easy was it for you to press the button to start the injection?
3. How easy was the autoinjector to use? 4. How easy was it to hold the autoinjector throughout the injection?
5. How easy was it for you to inject yourself using the autoinjector?
6.
How easy was it to follow the progress of the injection?
Each question was answered on a scale from 1 (Very difficult) to 5 (Very easy).
The percentage of participants who scored either a 4 (Somewhat easy) or 5 (Very easy) on each question is reported.
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At the end of each treatment period; Week 4 and Week 8
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Certainty of Completing the Injection With the Autoinjector
Zeitfenster: At the end of each treatment period; Week 4 and Week 8
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Certainty of completing the injection with the autoinjector was assessed based on responses to Question 7 of the Subject's Experience with the Autoinjector Questionnaire: "How certain were you that you knew when the injection was finished?"
Participants answered on a scale from 1 (Not at all) to 5 (Extremely).
The percentage of participants who scored 4 (Very) or 5 (Extremely) is reported.
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At the end of each treatment period; Week 4 and Week 8
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Convenience
Zeitfenster: At the end of each treatment period; Week 4 and Week 8
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Convenience was assessed based on responses to Question 8 of the Subject's Experience with the Autoinjector Questionnaire: "How convenient was the autoinjector to use?" Participants answered on a scale from 1 (Not at all) to 5 (Very much).
The percentage of participants who scored a 4 (Quite a bit) or 5 (Very much) is reported.
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At the end of each treatment period; Week 4 and Week 8
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Discomfort
Zeitfenster: At the end of each treatment period; Week 4 and Week 8
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Discomfort was assessed based on responses to Question 9 of the Subject's Experience with the Autoinjector Questionnaire: "How much discomfort did you experience when giving yourself the medicine using the autoinjector?"
Participants answered on a scale from 1 (None) to 5 (Very much).
The percentage of participants who scored a 1 (None) or 2 (A little) is reported.
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At the end of each treatment period; Week 4 and Week 8
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Satisfaction
Zeitfenster: At the end of each treatment period; Week 4 and Week 8
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Satisfaction was assessed based on responses to questions 11 and 12 of the Subject's Experience with the Autoinjector Questionnaire.
Question 11: "How dependable (durable, sturdy, reliable) did you feel the autoinjector device was?" answered on a scale from 1 (Not at all) to 5 (Very much).
Question 12: "Overall, how likely would you be to recommend the autoinjector to someone like you who is on etanercept?" answered on a scale from 1 (Would not recommend) to 5 (Highly likely to recommend).
The percentage of participants who scored either a 4 or 5 on each question is reported.
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At the end of each treatment period; Week 4 and Week 8
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Pain Associated With Use of the Autoinjector
Zeitfenster: At the end of each treatment period; Week 4 and Week 8
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Pain associated with use of the autoinjector was assessed based on responses to Question 10 of the Subject's Experience with the Autoinjector Questionnaire: "Using this scale, select the circle that best describes how much it hurt when giving yourself an injection."
Participants answered on a scale from 0 (No hurt) to 5 (Hurts worst).
The percentage of participants who scored a 0 (No hurt) or 1 (Hurts a little bit) is reported.
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At the end of each treatment period; Week 4 and Week 8
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Strength of Preference for Autoinjector A and Autoinjector B
Zeitfenster: Week 8
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Strength of preference for Autoinjector A versus Autoinjector B was assessed by Question 2 of the Subject Preference Questionnaire administered after the completion of the two treatment periods at Week 8.
After selecting which autoinjector they preferred overall, participants were asked to indicate how much they preferred it on a scale from 1 (Slightly), 2 (Somewhat), 3 (Strongly) and 4 (Vey Strongly).
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Week 8
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Mitarbeiter und Ermittler
Sponsor
Publikationen und hilfreiche Links
Nützliche Links
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
- Hautkrankheiten
- Erkrankungen des Immunsystems
- Autoimmunerkrankungen
- Gelenkerkrankungen
- Erkrankungen des Bewegungsapparates
- Rheumatische Erkrankungen
- Bindegewebserkrankungen
- Hautkrankheiten, papulosquamös
- Arthritis
- Arthritis, Rheuma
- Schuppenflechte
- Physiologische Wirkungen von Arzneimitteln
- Agenten des peripheren Nervensystems
- Analgetika
- Agenten des sensorischen Systems
- Entzündungshemmende Mittel, nichtsteroidal
- Analgetika, nicht narkotisch
- Entzündungshemmende Mittel
- Antirheumatika
- Immunsuppressive Mittel
- Immunologische Faktoren
- Magen-Darm-Mittel
- Etanercept
Andere Studien-ID-Nummern
- 20090176
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Produkt, das in den USA hergestellt und aus den USA exportiert wird
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
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