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Safety and Effect on Quality of Life/Work Productivity of Humira in Patients With Rheumatoid Arthritis (AGIL)

10. september 2018 oppdatert av: AbbVie (prior sponsor, Abbott)

Long Term Documentation of the Safety and Efficacy as Well as the Effects on Quality of Life and Work Productivity in Patients With Rheumatoid Arthritis Under HUMIRA® (Adalimumab) in Routine Clinical Practice (AGIL)

The AGIL study was designed to evaluate the effectiveness and safety of adalimumab over 5 years in routine daily clinical practice in Germany, with a focus on the impact of therapy on employment-related outcomes.

Studieoversikt

Status

Fullført

Forhold

Studietype

Observasjonsmessig

Registrering (Faktiske)

7229

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 99 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

Community sample: Patients with rheumatoid arthritis

Beskrivelse

Inclusion Criteria:

  • Moderate to severe active rheumatoid arthritis in adults with insufficient response to disease-modifying antirheumatic drugs
  • Inclusive methotrexate
  • Moderate to severe active rheumatoid arthritis in adults who have not been treated with methotrexate before; In case of incompatibility with methotrexate, Humira can be used as monotherapy.

Exclusion Criteria:

  • Hypersensitivity against the drug or one of the other ingredients
  • Active tuberculosis or other severe infections (e.g. sepsis and opportunistic infections)
  • Moderate to severe cardiac insufficiency

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Observasjonsmodeller: Bare etui
  • Tidsperspektiver: Potensielle

Kohorter og intervensjoner

Gruppe / Kohort
Adalimumab
Adults with moderate to severe active rheumatoid arthritis (RA) who initiated adalimumab therapy during routine clinical care.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change From Baseline in Number of Missed Working Days Due to Sick Leave in the Past 6 Months
Tidsramme: Baseline and 6, 12, 24, 36, 48, and 60 months
Primary effectiveness outcomes related to employment were performed in patients who were employed part- or full-time at baseline. Sick leave days were based on patient recall.
Baseline and 6, 12, 24, 36, 48, and 60 months
Percentage of Participants With > 5 Missed Working Days Due to Sick Leave in the Past 6 Months
Tidsramme: Baseline, 6, 12, 24, 36, 48, and 60 months
Primary effectiveness outcomes related to employment were performed in patients who were employed part- or full-time at baseline. Sick leave days were based on patient recall.
Baseline, 6, 12, 24, 36, 48, and 60 months
Change From Baseline in Work Productivity and Activity Impairment: Absenteeism
Tidsramme: Baseline and 3, 6, 12, 24, 36, 48, and 60 months

The Work Productivity and Activity Impairment (WPAI) questionnaire for general health is a validated tool in RA consisting of 6 questions, based on patient recall of the previous 7 days. WPAI assesses work time missed due to illness (absenteeism), impairment at work due to health (presenteeism), total work productivity impairment due to health (an aggregate measure of both absenteeism and presenteeism), and total non-occupational activity impairment due to health.

WPAI scores are expressed as impairment percentages, with higher scores indicating worse outcomes.

Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Change From Baseline in Work Productivity and Activity Impairment: Presenteeism
Tidsramme: Baseline and 3, 6, 12, 24, 36, 48, and 60 months

The Work Productivity and Activity Impairment (WPAI) questionnaire for general health is a validated tool in RA consisting of 6 questions, based on patient recall of the previous 7 days. WPAI assesses work time missed due to illness (absenteeism), impairment at work due to health (presenteeism), total work productivity impairment due to health (an aggregate measure of both absenteeism and presenteeism), and total non-occupational activity impairment due to health.

WPAI scores are expressed as impairment percentages, with higher scores indicating worse outcomes.

Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Change From Baseline in Work Productivity and Activity Impairment: Total Work Productivity Impairment
Tidsramme: Baseline and 3, 6, 12, 24, 36, 48, and 60 months

The Work Productivity and Activity Impairment (WPAI) questionnaire for general health is a validated tool in RA consisting of 6 questions, based on patient recall of the previous 7 days. WPAI assesses work time missed due to illness (absenteeism), impairment at work due to health (presenteeism), total work productivity impairment due to health (an aggregate measure of both absenteeism and presenteeism), and total non-occupational activity impairment due to health.

WPAI scores are expressed as impairment percentages, with higher scores indicating worse outcomes.

Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Change From Baseline in Work Productivity and Activity Impairment: Total Activity Impairment
Tidsramme: Baseline and 3, 6, 12, 24, 36, 48, and 60 months

The Work Productivity and Activity Impairment (WPAI) questionnaire for general health is a validated tool in RA consisting of 6 questions, based on patient recall of the previous 7 days. WPAI assesses work time missed due to illness (absenteeism), impairment at work due to health (presenteeism), total work productivity impairment due to health (an aggregate measure of both absenteeism and presenteeism), and total non-occupational activity impairment due to health.

WPAI scores are expressed as impairment percentages, with higher scores indicating worse outcomes.

Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Change From Baseline in Work Activity Index (WAI)
Tidsramme: Baseline and 6, 12, 24, 36, 48, and 60 months
The WAI is a tool designed to record the work ability of employees and consists of 7 questions. The modified WAI used in this study included Questions 1, 2, 4, 6, and 7 of the WAI. Question 3, which involves the number of current diseases diagnosed by a physician, was omitted because this parameter was unlikely to reflect change due to treatment. Question 5 (sick leave during the past year) was replaced with the previous question concerning sick leave days.WAI scores range from 7 (worst) to 49 (best).
Baseline and 6, 12, 24, 36, 48, and 60 months
Change From Baseline in Disease Activity Score - 28 Joints (DAS28)
Tidsramme: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
The DAS28 is a validated index of rheumatoid arthritis disease activity. Twenty-eight tender joint counts, 28 swollen joint counts, erythrocyte sedimentation rate (ESR), and the patient's assessment of global disease activity are included in the DAS28 score. Scores on the DAS28 range from 0 to 10. A DAS28 score > 5.1 indicates high disease activity, a DAS28 score < 3.2 indicates low disease activity, and a DAS28 score < 2.6 indicates clinical remission.
Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Change From Baseline in Tender Joint Count
Tidsramme: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Twenty-eight joints were assessed and classified as tender/not tender by pressure and joint manipulation on physical examination.
Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Change From Baseline in Swollen Joint Count
Tidsramme: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Twenty-eight joints were assessed and classified as swollen/not swollen by pressure and joint manipulation on physical examination.
Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Change From Baseline in Erythrocyte Sedimentation Rate
Tidsramme: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Change From Baseline in C-reactive Protein
Tidsramme: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Change From Baseline in Health-Assessment Questionnaire-Disability Index (HAQ-DI)
Tidsramme: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
The HAQ-DI is a patient-reported assessment of physical function that includes 20 items in eight categories representing a comprehensive set of functional activities, including dressing, eating, walking, and hygiene. Patients are asked about their ability to complete these tasks in the past week using the following categories: without any difficulty (0); with some difficulty (1); with much difficulty (2); and unable to do (3). Scores on each task were summed and averaged to provide an overall score ranging from 0 (best) to 3 (worst), with a higher score representing a high-dependency disability.
Baseline and 3, 6, 12, 24, 36, 48, and 60 months
EuroQol-5 Dimensions (EQ-5D) Scores
Tidsramme: Baseline and 3, 6, 12, 24, 36, 48, and 60 months

The EuroQol-5 Dimensions (EQ-5D) is a generic instrument for measuring health-related quality of life. The patient questionnaire consists of two parts. The first part includes statements for the following five areas (dimensions):

  • agility/mobility
  • self-care
  • usual activities
  • pain, bodily discomfort
  • anxiety, depression

For each dimension the patient is asked for a three-level assessment of their health on the current day: "no problems" (1), "some problems" (2), "extreme problems" (3).

Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Change From Baseline in Euroqol Visual Analog Scale (VAS)
Tidsramme: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
EuroQol-5 Dimensions (EQ-5D): The EQ-5D is a generic instrument for measuring health-related quality of life. The patient questionnaire consists of two parts. The second part is a vertical, thermometer-like, VAS ranging from 0 to 100 that provides a patient-reported assessment of overall health. Patients are asked to mark how good or bad their health is on that day, with 100 meaning "the best health you can imagine" and 0 meaning "the worst health you can imagine."
Baseline and 3, 6, 12, 24, 36, 48, and 60 months

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Number of Physician Visits in Past 6 Months
Tidsramme: Baseline, 6, 12, 24, 36, 48, and 60 months
Participants self-reported the number of physician visits they had in the past 6 months.
Baseline, 6, 12, 24, 36, 48, and 60 months
Number of Inpatient Hospitalizations in Past 6 Months
Tidsramme: Baseline, 6, 12, 24, 36, 48, and 60 months
Participants self-reported the number of hospitalizations they had in the past 6 months.
Baseline, 6, 12, 24, 36, 48, and 60 months
Duration of Inpatient Hospitalizations in Past 6 Months
Tidsramme: Baseline, 6, 12, 24, 36, 48, and 60 months
Participants who had been hospitalized were asked how many days they were hospitalized in the past 6 months.
Baseline, 6, 12, 24, 36, 48, and 60 months
Number of Days With Impairment of Non-Occupational Activities in Past 6 Months
Tidsramme: Baseline, 6, 12, 24, 36, 48, and 60 months
Patients reported the number of days that sickness affected non-occupational activities in four categories: household, child-rearing/parenting, education, and recreational (free-time). Participants with no impairment were considered to have 0 days.
Baseline, 6, 12, 24, 36, 48, and 60 months
Duration of Morning Stiffness
Tidsramme: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Participant's Assessment of Pain
Tidsramme: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Participants were asked to evaluate their level of pain in the past 7 days on a scale from 0 (no pain) to 10 (unbearable pain).
Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Participant's Assessment of Fatigue
Tidsramme: Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Participants were asked to indicate how much they had suffered from abnormal exhaustion and fatigue during the past 7 days on a scale from 0 (none) to 10 (strongly).
Baseline and 3, 6, 12, 24, 36, 48, and 60 months
Percentage of Participants Taking Concomitant RA Medications
Tidsramme: Baseline to month 60
Assessment of concomitant medications included disease-modifying antirheumatic drugs (DMARDs) (methotrexate, Leflunomid, sulfasalazine), systemic glucocorticoids, non-steroidal anti-inflammatory drugs (NSAIDs), Cox-2 inhibitors (coxibs), analgesics and others.
Baseline to month 60
Patient Assessment of Adalimumab Therapy
Tidsramme: Months 3, 6, 12, 24, 36, 48, and 60

Participants were asked to rate therapy with adalimumab in comparison with other previous therapies according to the following response options:

  • Considerably better
  • Better
  • About the same
  • Worse
  • Noticeably worse
Months 3, 6, 12, 24, 36, 48, and 60

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Studieleder: Henning Kleine, PhD, AbbVie Deutschland GmbH & Co. KG, Medical Department

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Hjelpsomme linker

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

12. januar 2009

Primær fullføring (Faktiske)

14. september 2017

Studiet fullført (Faktiske)

14. september 2017

Datoer for studieregistrering

Først innsendt

24. februar 2010

Først innsendt som oppfylte QC-kriteriene

24. februar 2010

Først lagt ut (Anslag)

26. februar 2010

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

7. februar 2019

Siste oppdatering sendt inn som oppfylte QC-kriteriene

10. september 2018

Sist bekreftet

1. august 2018

Mer informasjon

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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