Basic Documentation of Adalimumab (Humira) in Patients With Ankylosing Spondylitis (AS)
10. června 2015 aktualizováno: AbbVie (prior sponsor, Abbott)
Safety and Effectiveness of Adalimumab in Patients With Ankylosing Spondylitis in Routine Clinical Practice
The research question explored in this study was whether the effectiveness and safety of adalimumab in participants with ankylosing spondylitis was maintained during long-term therapy in routine clinical practice in Germany.
Přehled studie
Postavení
Dokončeno
Podmínky
Detailní popis
This was a postmarketing observational study (PMOS) for participants with insufficiently controlled, moderate to severe, active AS who were eligible for adalimumab therapy.
Participants started treatment with adalimumab under normal clinical settings in Germany.
Enrolled participants were followed during adalimumab therapy .
Participants were assessed during regular clinic visits for up to 24 months and 359 clinicians (rheumatologists/orthopedists/general practitioners/internist) participated in the study.
Since this was an observational trial, not all doctors followed the stated age limitations and some participants under the age of 18 were enrolled.
Typ studie
Pozorovací
Zápis (Aktuální)
4681
Kritéria účasti
Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.
Kritéria způsobilosti
Věk způsobilý ke studiu
18 let a starší (Dospělý, Starší dospělý)
Přijímá zdravé dobrovolníky
Ne
Pohlaví způsobilá ke studiu
Všechno
Metoda odběru vzorků
Vzorek nepravděpodobnosti
Studijní populace
Participants with AS in routine clinical practice.
Popis
Inclusion Criteria:
- Participants with active, AS for at least 4 weeks (BASDAI greater than or equal to 4).
- Participants who failed treatment with two non-steroidal anti-inflammatory drugs (NSAIDs).
- No contraindications for anti-tumor necrosis factors (TNF) therapy.
Exclusion Criteria:
1. Participants who do not meet the above listed inclusion criteria.
Studijní plán
Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.
Jak je studie koncipována?
Detaily designu
- Observační modely: Pouze případ
- Časové perspektivy: Budoucí
Kohorty a intervence
Skupina / kohorta |
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Ankylosing spondylitis
Participants with ankylosing spondylitis
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Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
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Mean Change From Baseline in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) Score
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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The BASDAI was a six question, participant-reported measure of overall disease activity that probed the level of fatigue, neck/back/hip pain, peripheral joint swelling and pain, localized tenderness, as well as morning stiffness severity and duration.
It was scored on a numerical rating scale that ranged from 0 (no symptoms) to 10 (severe symptoms), and the minimum clinically important difference (MCID) was 1.0.
The final BASDAI score was calculated using the following equation, in which 01 - 06 represents the question number: (BASDAI01 + BASDAI02 + BASDAI03 + BASDAI04 + BASDAI05/2 + BASDAI06*1.25/2)/5.
The scale for question 6 was reduced to 0-8 since BASDAI06 was multiplied by 1.25.
Data are reported as the mean change total score from baseline (Month 0).
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Mean Change From Baseline in Bath Ankylosing Spondylitis Functional Index (BASFI) Score
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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The BASFI was a ten question, participant-reported measure that evaluated physical function.
Each question was scored on a numerical rating scale that ranged from 0 (no functional impairment) to 10 (maximal impairment), and the MCID was 0.7.
The mean of the ten questions was the total BASFI score.
Data are reported as the mean change of total score from baseline (Month 0).
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Number of Participants With Drug-Related Adverse Events (AEs)
Časové okno: From signing of informed consent up to 24 months
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An adverse event/adverse experience was any reaction, side effect or other untoward event associated with the use of a drug in humans, whether or not the event was considered drug related.
This included adverse events occurring from accidental or deliberate drug overdose, from drug abuse, or from drug withdrawal.
Exacerbations of pre-existing conditions are also considered adverse events.
Data presented are adverse events that are drug-related and are detailed in the adverse event section of this report.
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From signing of informed consent up to 24 months
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Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Mean Number of Involved Peripheral Joints
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Peripheral joints were assessed by Tender Joint Counts (TJC) and Swollen Joint Counts (SJC), using pressure and joint manipulation during physical examination.
Seventy-eight TJC and 76 SJC were evaluated and a score of 0 (not tender or swollen) or 1 (tender or swollen) was assigned for each joint with a higher total score indicating a greater number of involved joints.
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Percentage of Participants With Extraspinal Manifestations
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Extraspinal manifestations (enthesitis, dactylitis, uveitis, psoriasis, and Inflammatory Bowel Disease (IBD)) were assessed by investigators and reported on the basis of their clinical evaluation and participant records.
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Mean Erythrocyte Sedimentation Rate (ESR)
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Plasma concentrations of ESR were assessed as a marker of systemic inflammation that provided insights into the overall anti-inflammatory effect of rheumatologic therapies.
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Mean Plasma Concentrations of C-Reactive Protein (CRP)
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Plasma concentrations of CRP were assessed as a marker of systemic inflammation that provided insights into the overall anti-inflammatory effect of rheumatologic therapies.
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Mean Bath Ankylosing Spondylitis-Global (BAS-G) Score
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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The BAS-G was a participant-reported instrument with two items.
In the first item, the participant rated the effect of their disease over the last week, and in the second item, the participant rated the effect of their disease over the previous 6 months.
Each item of the BAS-G was scored on a scale ranging from 0 (no effect) to 10 (very severe effect).
The mean of the two scores was the total BAS-G score and the MCID was 1.5.
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Mean Global Assessment of Disease Activity Score
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Global Assessment of Disease Activity was a participant-reported measure that evaluated disease activity.
It was scored on a scale that ranged from 0 to 10; lower scores indicated better patient status.
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Mean Participant Fatigue Score
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Using the BASDAI questionnaire, participants assessed the overall level of fatigue/tiredness experienced by him/her.
It was scored on a numerical rating scale from 0 (no symptoms) to 10 (severe symptoms).
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Mean Participant Pain Score
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Using the BASDAI questionnaire, participants assessed the overall level of AS neck, back or hip pain experienced by him/her.
It was scored on a numerical rating scale from 0 (no symptoms) to 10 (severe symptoms).
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Percentage of Participants With Morning Stiffness
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Morning stiffness was a participant-reported assessment.
The number of participants with morning stiffness were assessed at each visit.
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Mean Duration of Morning Stiffness
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Participants accessed the duration of morning stiffness in 15 minute intervals from 0 to 2 hours.
Data are reported as the mean duration of morning stiffness ± standard deviation.
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Percentage of Participants Achieving Assessment of SpondyloArthritis International Society (ASAS) Improvement Criteria
Časové okno: At 3, 6, 9, 12, 18, and 24 months
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This is a four domain (participant global assessment of disease activity, assessment of spinal pain, assessment of function (BASFI), and assessment of duration/severity of morning stiffness (mean of BASDAI questions 5 and 6)), participant-reported assessment scored on a scale from 0 (best) to 10 (worst).
To qualify for a 20% improvement, participants were required to have an improvement of greater than or equal to 20% and greater than or equal to 1 unit in at least 3 domains, and no worsening of greater than or equal to 20% and greater than or equal to 1 unit in the remaining domain.
To achieve a 40% improvement, participants were required to have an improvement of greater than or equal to 40% and greater than or equal to 2 units in at least 3 domains, and no worsening at all in the remaining domain.
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At 3, 6, 9, 12, 18, and 24 months
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Percentage of Participants Achieving ASAS Partial Remission Criteria
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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This is a four domain (participant global assessment of disease activity, assessment of spinal pain, assessment of function (BASFI), and assessment of duration/severity of morning stiffness (mean of BASDAI questions 5 and 6)), participant-reported assessment scored on a scale from 0 (best) to 10 (worst).
To qualify for a partial remission, participants had to have values of 2 or less (on a scale of 10) in each of the 4 domains.
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Percentage of Participants With Impairment in Daily Activities During the Last 4 Weeks
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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The impairment of daily activities was based on participant recall of events that occurred over the 4 weeks before the visit.
Percentage of participants with impairment for 0, less than 7, 7 to 14, and greater than 14 days was assessed.
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Percentage of Participants Who Missed Work Days Due to Ankylosing Spondylitis (AS) in the Previous 12 Months
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Mean Missed Work Days Due to Ankylosing Spondylitis in the Previous 12 Months
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Percentage of Participants With In-Patient Hospitalization Due to Ankylosing Spondylitis in the Previous 12 Months
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Mean Days of In-Patient Hospitalization Due to Ankylosing Spondylitis in the Previous 12 Months
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Percentage of Participants on Adalimumab Monotherapy
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Percentage of Participants With Concomitant Non-Biologic Disease-modifying Antirheumatic Drugs (DMARDs)
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Percentage of Participants With Concomitant Pain Relief/Anti-Inflammatory Agents
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Participants with concomitant pain relief/anti-inflammatory agents like analgesics, non-steroidal anti-inflammatory drugs (NSAIDs), cyclooxygenase-2 (COX-2) inhibitors, and systemic glucocorticoids were assessed during the study period.
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Mean Equivalent Dose of Prednisolone
Časové okno: At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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The mean equivalent dose of prednisolone was calculated based on the International Standard for comparison of different glucocorticoid products.
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At Baseline (Month 0), 3, 6, 9, 12, 18, and 24 months
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Spolupracovníci a vyšetřovatelé
Zde najdete lidi a organizace zapojené do této studie.
Sponzor
Vyšetřovatelé
- Ředitel studie: Bianca Wittig, MD, AbbVie Deutschland GmbH & Co. KG, Medical Department
Publikace a užitečné odkazy
Osoba odpovědná za zadávání informací o studiu tyto publikace poskytuje dobrovolně. Mohou se týkat čehokoli, co souvisí se studiem.
Užitečné odkazy
Termíny studijních záznamů
Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.
Hlavní termíny studia
Začátek studia
1. ledna 2006
Primární dokončení (Aktuální)
1. května 2014
Dokončení studie (Aktuální)
1. května 2014
Termíny zápisu do studia
První předloženo
1. března 2010
První předloženo, které splnilo kritéria kontroly kvality
2. března 2010
První zveřejněno (Odhad)
3. března 2010
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Odhad)
9. července 2015
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
10. června 2015
Naposledy ověřeno
1. června 2015
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
Další identifikační čísla studie
- P10-147
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .