Current Adoption of Composite Indices in Evaluating Rheumatoid Arthritis Patients: An Observational Study (New Indices)
31 grudnia 2012 zaktualizowane przez: Pfizer
Current Adoption Of Composite Indices In Evaluating Rheumatoid Arthritis Patients: An Observational Study ("NEW INDICES Study")
This is an observational study of composite indices, including the CLARA (CLinical ARthritis Activity) index, in rheumatoid arthritis (RA) patients in routine clinical practice in Italy in order to evaluate clinical remission and low disease activity.
Data will be collected only from patients providing informed consent.
In this study we aimed to assess the psychometric properties of a new composite instrument termed CLinical ARthritis Activity (PRO-CLARA) that uses only three PRO measures from among the 7 ACR Core Data Set.
We hypothesized that this index would facilitate rapid and easy RA activity assessment in daily routine.
Przegląd badań
Szczegółowy opis
All patients who respond to inclusion/exclusion criteria at baseline will be considered valuable for the analysis.
Typ studiów
Obserwacyjny
Zapisy (Rzeczywisty)
293
Kontakty i lokalizacje
Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.
Lokalizacje studiów
-
-
-
Torino, Włochy, 10128
- Pfizer Investigational Site
-
-
Kryteria uczestnictwa
Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.
Kryteria kwalifikacji
Wiek uprawniający do nauki
18 lat i starsze (Dorosły, Starszy dorosły)
Akceptuje zdrowych ochotników
Nie
Płeć kwalifikująca się do nauki
Wszystko
Metoda próbkowania
Próbka prawdopodobieństwa
Badana populacja
primary care clinic
Opis
Inclusion Criteria:
- Eighteen years of age or older with diagnosis of RA based on the 1987 American College of Rheumatology (ACR) criteria and in accordance with local guidelines.
- Patients eligible to anti-TNF therapy
- Patients naïve to anti-TNFa drugs
- Patients with radiography (hands and feet) executed by 6 months before the baseline or at baseline according to modified Sharp Van der Hejde method [Sharp JT et al. 1985; Sharp JT. Et al. 1989; Van der Heijde DM et al. 1989] Patients capable of understanding and completing the questionnaire Patients capable of understanding and signing an informed consent form
Exclusion Criteria:
- Patients with tumors
- Patients already included in clinical trials
Plan studiów
Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.
Jak projektuje się badanie?
Szczegóły projektu
Kohorty i interwencje
Grupa / Kohorta |
Interwencja / Leczenie |
|---|---|
|
1
As per routine clinical care
|
As per routine clinical care
Inne nazwy:
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Percentage of Participants With Remission as Per Modified American College of Rheumatology (Modified ACR) Criteria at Month 6
Ramy czasowe: Month 6
|
Modified ACR: participant considered in RA remission if at any time point 1) participant satisfied all of the following criteria: tender joint count(TJC) less than or equal to(<=)1;swollen joint count(SJC)<=1 (TJC, SJC based on 28-joints);C-reactive protein(CRP)<=1 milligram/deciliter(mg/dL); patient global assessment (PtGA) <=1 (assessed on 0-10 centimeter[cm] visual analog scale[VAS]) or 2) participant had Simplified Disease Activity Index score of <=3.3 (SDAI, numerical sum of 5 outcome parameters: TJC, SJC, PtGA, physician global assessment [PGA, assessed on 0-10 cm VAS], and CRP [mg/dL]).
|
Month 6
|
|
Percentage of Participants With Remission as Per Modified American College of Rheumatology (Modified ACR) Criteria at Month 12
Ramy czasowe: Month 12
|
Modified ACR: participant was considered in RA remission if at any time point 1) participant satisfied all of the following criteria: TJC <=1; SJC <=1 (TJC, SJC based on 28-joints); CRP <=1 mg/dL; PtGA<=1 (assessed on 0-10 centimeter[cm] visual analog scale[VAS]) or 2) participant had SDAI score of <=3.3 (SDAI: the numerical sum of 5 outcome parameters: TJC, SJC, PtGA, PGA [assessed on 0-10 cm VAS], and CRP [mg/dL]).
|
Month 12
|
|
Minimal Disease Activity: Outcome Measures in Rheumatology Arthritis Clinical Trials (OMERACT) at Month 6
Ramy czasowe: Month 6
|
OMERACT minimal disease activity: participant considered with minimal disease activity if he/she met 5 of 7 criteria: Pain <=2 (assessed on a 0-10 cm VAS, 0 cm=no pain and 10 cm=worst possible pain); SJC <=1; TJC <=1 (SJC, TJC based on 28-joints); Health Assessment Questionnaire (HAQ) <=0.5 (assessment of ability to perform task on 0-3 point scale, 0=least difficulty and 3=extreme difficulty); PGA <=1.5;
PtGA <=2 (PGA, PtGA: assessed on 0-10 cm VAS, higher score = greater affection due to disease activity); erythrocyte sedimentation rate (ESR) <=20 millimeter per hour (mm/hr).
|
Month 6
|
|
Minimal Disease Activity: Outcome Measures in Rheumatology Arthritis Clinical Trials (OMERACT) at Month 12
Ramy czasowe: Month 12
|
OMERACT minimal disease activity: participant considered with minimal disease activity if he/she met 5 of 7 criteria: Pain <=2 (assessed on a 0-10 cm VAS, 0 cm=no pain and 10 cm=worst possible pain); SJC <=1; TJC <=1 (SJC, TJC based on 28-joints); HAQ <=0.5 (assessment of ability to perform task on 0-3 point scale, 0=least difficulty and 3=extreme difficulty); PGA <=1.5;
PtGA <=2 (PGA, PtGA: assessed on 0-10 cm VAS, higher score = greater affection due to disease activity); ESR <=20 mm/hr.
|
Month 12
|
|
Minimal Disease Activity: Italian Group for the Study of Early Arthritis (GISEA) at Month 6
Ramy czasowe: Month 6
|
GISEA minimal disease activity criteria: a participant was considered with minimal disease activity if he/she met the following criteria: SJC <=2 (based on 28-joints); HAQ <=0.5 (assessment of ability to perform task on 0-3 point scale, 0=least difficulty and 3=extreme difficulty); and ESR <=20 mm/hr.
|
Month 6
|
|
Minimal Disease Activity: Italian Group for the Study of Early Arthritis (GISEA) at Month 12
Ramy czasowe: Month 12
|
GISEA minimal disease activity criteria: a participant was considered with minimal disease activity if he/she met the following criteria: SJC <=2 (based on 28-joints); HAQ <=0.5 (assessment of ability to perform task on 0-3 point scale, 0=least difficulty and 3=extreme difficulty); and ESR <=20 mm/hr.
|
Month 12
|
|
Number of Swollen Joints (SJC) and Tender Joints (TJC) at Month 6
Ramy czasowe: Month 6
|
Number of swollen joints was determined by examination of 28 joints and identifying when swelling was present. The number of swollen joints was recorded on the joint assessment form at each visit, no swelling = 0, swelling =1. Number of tender joints was determined by examining 28 joints and identified the joints that were painful under pressure or to passive motion. The number of tender joints was recorded on the joint assessment form at each visit, no tenderness = 0, tenderness = 1. |
Month 6
|
|
Number of Swollen Joints (SJC) and Tender Joints (TJC) at Month 12
Ramy czasowe: Month 12
|
Number of swollen joints was determined by examination of 28 joints and identifying when swelling was present. The number of swollen joints was recorded on the joint assessment form at each visit, no swelling = 0, swelling =1. Number of tender joints was determined by examining 28 joints and identified the joints that were painful under pressure or to passive motion. The number of tender joints was recorded on the joint assessment form at each visit, no tenderness = 0, tenderness = 1. |
Month 12
|
|
Disease Activity Score Based on 28-joints Count (DAS28) at Month 6
Ramy czasowe: Month 6
|
DAS28 calculated from SJC and TJC using the 28 joints count, the ESR (mm/hr) and PtGA of disease activity (participant rated arthritis activity assessment with transformed scores ranging 0 to 10 cm VAS; higher scores indicated greater affectation due to disease activity).
Total score range: 0 to 9.4, higher score indicated more disease activity.
DAS28 <= 3.2 implied low disease activity and > 3.2 to 5.1 implied moderate to high disease activity, and DAS28 < 2.6 = remission.
|
Month 6
|
|
Disease Activity Score Based on 28-joints Count (DAS28) at Month 12
Ramy czasowe: Month 12
|
DAS28 calculated from SJC and TJC using the 28 joints count, the ESR (mm/hr) and PtGA of disease activity (participant rated arthritis activity assessment with transformed scores ranging 0 to 10 cm VAS; higher scores indicated greater affectation due to disease activity).
Total score range: 0 to 9.4, higher score indicated more disease activity.
DAS28 <= 3.2 implied low disease activity and > 3.2 to 5.1 implied moderate to high disease activity, and DAS28 < 2.6 = remission.
|
Month 12
|
|
Simplified Disease Activity Index (SDAI) at Month 6
Ramy czasowe: Month 6
|
The SDAI is the numerical sum of five outcome parameters: TJC and SJC (based on a 28-joint assessment), PtGA and PGA (assessed on 0-10 cm VAS; higher scores=greater affection due to disease activity), and CRP (mg/dL).
SDAI total score= 0-86.
SDAI <=3.3 indicates disease remission, >3.4 to 11 = low disease activity, >11 to 26 = moderate disease activity, and >26 = high disease activity.
|
Month 6
|
|
Simplified Disease Activity Index (SDAI) at Month 12
Ramy czasowe: Month 12
|
The SDAI is the numerical sum of five outcome parameters: TJC and SJC (based on a 28-joint assessment), PtGA and PGA (assessed on 0-10 cm VAS; higher scores=greater affection due to disease activity), and CRP (mg/dL).
SDAI total score= 0-86.
SDAI <=3.3 indicates disease remission, >3.4 to 11 = low disease activity, >11 to 26 = moderate disease activity, and >26 = high disease activity.
|
Month 12
|
|
Rheumatoid Arthritis Disease Activity Index (RADAI) at Month 6
Ramy czasowe: Month 6
|
RADAI:self-assessed measure of disease activity in RA.
Consists of 5 items: global disease activity(GDA) in past 6 months; current disease activity(CDA) as measured by SJC and TJC; current arthritis pain; current duration of morning stiffness; current TJC.
GDA,CDA and pain were scored on an 11-point numerical rating scale,0=no disease activity/pain to 10=extreme disease activity/pain.
Current morning stiffness and TJC were transformed to a 0-10 point scale,higher scores=more disease activity.
RADAI total score=sum of individual items divided by 5;range 0-10, higher score=more disease activity.
|
Month 6
|
|
Rheumatoid Arthritis Disease Activity Index (RADAI) at Month 12
Ramy czasowe: Month 12
|
RADAI:self-assessed measure of disease activity in RA.
Consists of 5 items: GDA in past 6 months; CDA as measured by SJC and TJC; current arthritis pain; current duration of morning stiffness; current TJC.
GDA,CDA and pain were scored on an 11-point numerical rating scale,0=no disease activity/pain to 10=extreme disease activity/pain.
Current morning stiffness and TJC were transformed to a 0-10 point scale,higher scores=more disease activity.
RADAI total score=sum of individual items divided by 5;range 0-10, higher score=more disease activity.
|
Month 12
|
|
Clinical Disease Activity Index (CDAI) at Month 6
Ramy czasowe: Month 6
|
The CDAI is the numerical sum of 4 outcome parameters: TJC and SJC (based on a 28-joint assessment), PtGA and PGA (assessed on 0-10 cm VAS; higher scores=greater affection due to disease activity).
CDAI total score = 0-76.
CDAI <= 2.8 indicates disease remission, >2.8 to 10 = low disease activity, >10 to 22 = moderate disease activity, and >22 = high disease activity.
|
Month 6
|
|
Clinical Disease Activity Index (CDAI) at Month 12
Ramy czasowe: Month 12
|
The CDAI is the numerical sum of 4 outcome parameters: TJC and SJC (based on a 28-joint assessment), PtGA and PGA (assessed on 0-10 cm VAS; higher scores=greater affection due to disease activity).
CDAI total score = 0-76.
CDAI <= 2.8 indicates disease remission, >2.8 to 10 = low disease activity, >10 to 22 = moderate disease activity, and >22 = high disease activity.
|
Month 12
|
|
Patient Reported Outcomes - Clinical Arthritis Activity (PRO-CLARA ) at Month 6
Ramy czasowe: Month 6
|
PRO-CLARA:self-administered index of RA activity.
Consists of 3-items: participant's physical function (12 questions each scored on a 0 [without any difficulty] to 4 [unable to do] point scale); TJC(based on 16-joints, tenderness assessed on 0 [none] to 3 [severe] point scale); PtGA (participant rated disease activity on 0-10 cm VAS, 0=very well, 10 cm=very poorly).
Participant's physical function and TJC were transformed on a 0-10 point scale, higher scores=more disease activity.
PRO-CLARA total score=sum of scores of all 3 items divided by 3, range= 0-10, higher scores=more disease activity.
|
Month 6
|
|
Patient Reported Outcomes - Clinical Arthritis Activity (PRO-CLARA ) at Month 12
Ramy czasowe: Month 12
|
PRO-CLARA:self-administered index of RA activity.
Consists of 3-items: participant's physical function (12 questions each scored on a 0 [without any difficulty] to 4 [unable to do] point scale); TJC(based on 16-joints, tenderness assessed on 0 [none] to 3 [severe] point scale); PtGA (participant rated disease activity on 0-10 cm VAS, 0=very well, 10 cm=very poorly).
Participant's physical function and TJC were transformed on a 0-10 point scale, higher scores=more disease activity.
PRO-CLARA total score=sum of scores of all 3 items divided by 3, range= 0-10, higher scores=more disease activity.
|
Month 12
|
|
Clinical Arthritis Activity (CLARA) Index at Month 6
Ramy czasowe: Month 6
|
CLARA: index of RA activity.
Consists of 3-items: participant's physical function (12 questions each scored on a 0 [without any difficulty] to 4 [unable to do] point scale); TJC (based on 16-joints, tenderness assessed on 0 [none] to 3 [severe] point scale); SJC (based on 28-joints).
Each item was transformed on a 0-10 point scale, higher scores=more disease activity.
CLARA total score=sum of scores of all 3 items divided by 3, range= 0-10, higher scores=more disease activity.
|
Month 6
|
|
Clinical Arthritis Activity (CLARA) Index at Month 12
Ramy czasowe: Month 12
|
CLARA: index of RA activity.
Consists of 3-items: participant's physical function (12 questions each scored on a 0 [without any difficulty] to 4 [unable to do] point scale); TJC (based on 16-joints, tenderness assessed on 0 [none] to 3 [severe] point scale); SJC (based on 28-joints).
Each item was transformed on a 0-10 point scale, higher scores=more disease activity.
CLARA total score=sum of scores of all 3 items divided by 3, range= 0-10, higher scores=more disease activity.
|
Month 12
|
|
Patient Global Assessment (PtGA) of Disease Activity at Month 6
Ramy czasowe: Month 6
|
Participants answered: "Considering all the ways your arthritis affects you, how are you feeling today?"
Participants responded by using a 0 - 10 cm VAS, where 0 cm = very well and 10 cm = very poorly.
|
Month 6
|
|
Patient Global Assessment (PtGA) of Disease Activity at Month 12
Ramy czasowe: Month 12
|
Participants answered: "Considering all the ways your arthritis affects you, how are you feeling today?"
Participants responded by using a 0 - 10 cm VAS, where 0 cm = very well and 10 cm = very poorly.
|
Month 12
|
|
Physician Global Assessment (PGA) of Disease Activity at Month 6
Ramy czasowe: Month 6
|
Physician Global Assessment of Arthritis was measured on a 0 to 10 cm VAS, where 0 cm = very good and 10 cm = very bad.
|
Month 6
|
|
Physician Global Assessment (PGA) of Disease Activity at Month 12
Ramy czasowe: Month 12
|
Physician Global Assessment of Arthritis was measured on a 0 to 10 cm VAS, where 0 cm = very good and 10 cm = very bad.
|
Month 12
|
|
Visual Analog Fatigue Scale (VAFS) at Month 6
Ramy czasowe: Month 6
|
Participants assessed their fatigue using a 0 - 100 mm VAS, where 0 mm = no fatigue and 100 mm = worst possible fatigue.
|
Month 6
|
|
Visual Analog Fatigue Scale (VAFS) at Month 12
Ramy czasowe: Month 12
|
Participants assessed their fatigue using a 0 - 100 mm VAS, where 0 mm = no fatigue and 100 mm = worst possible fatigue.
|
Month 12
|
|
C-reactive Protein (CRP) at Month 6
Ramy czasowe: Month 6
|
The test for CRP is a laboratory measurement for evaluation of an acute phase reactant of inflammation through the use of an ultrasensitive assay.
Normal range of CRP is <1 mg/dL.
A decrease in the level of CRP indicates reduction in inflammation and therefore improvement.
|
Month 6
|
|
C-reactive Protein (CRP) at Month 12
Ramy czasowe: Month 12
|
The test for CRP is a laboratory measurement for evaluation of an acute phase reactant of inflammation through the use of an ultrasensitive assay.
Normal range of CRP is <1 mg/dL.
A decrease in the level of CRP indicates reduction in inflammation and therefore improvement.
|
Month 12
|
|
Erythrocyte Sedimentation Rate (ESR) at Month 6
Ramy czasowe: Month 6
|
ESR is a laboratory test that provides a non-specific measure of inflammation.
The test assesses the rate at which red blood cells fall in a test tube.
Normal range is 0-30 mm/hr.
A higher rate is consistent with inflammation.
|
Month 6
|
|
Erythrocyte Sedimentation Rate (ESR) at Month 12
Ramy czasowe: Month 12
|
ESR is a laboratory test that provides a non-specific measure of inflammation.
The test assesses the rate at which red blood cells fall in a test tube.
Normal range is 0-30 mm/hr.
A higher rate is consistent with inflammation.
|
Month 12
|
|
Number of Participants With Rheumatoid Factor (RF) at Month 6
Ramy czasowe: Month 6
|
RF is the auto antibody directed against immunoglobulin G (IgG) and its concentration is observed in human serum or plasma.
RF value higher than 20 units per milliliter (U/mL) is considered positive.
|
Month 6
|
|
Number of Participants With Rheumatoid Factor (RF) at Month 12
Ramy czasowe: Month 12
|
RF is the auto antibody directed against immunoglobulin G (IgG) and its concentration is observed in human serum or plasma.
RF value higher than 20 U/mL is considered positive.
|
Month 12
|
|
Patient's General Health Assessment at Month 6
Ramy czasowe: Month 6
|
Participants answered: "How would you describe your general health today?"
Participants assessed their general health using a 0 - 10 cm VAS, where 0 cm = very well and 10 cm = very poor.
|
Month 6
|
|
Patient's General Health Assessment at Month 12
Ramy czasowe: Month 12
|
Participants answered: "How would you describe your general health today?"
Participants assessed their general health using a 0 - 10 cm VAS, where 0 cm = very well and 10 cm = very poor.
|
Month 12
|
|
Patient Assessment of Arthritis Pain at Month 6
Ramy czasowe: Month 6
|
Participants rated the severity of arthritis pain on a 0 to 10 cm VAS, where 0 cm = no pain and 10 cm = most severe pain.
|
Month 6
|
|
Patient Assessment of Arthritis Pain at Month 12
Ramy czasowe: Month 12
|
Participants rated the severity of arthritis pain on a 0 to 10 cm VAS, where 0 cm = no pain and 10 cm = most severe pain.
|
Month 12
|
|
Duration of Morning Stiffness at Month 6
Ramy czasowe: Month 6
|
Duration of morning stiffness: Time elapsed when participant woke up in morning and was able to resume normal activities without stiffness in minutes.
Increase in stiffness duration from baseline represented disease progression and/or joint worsening, no change represented halting of disease progression, and a decrease represented improvement.
|
Month 6
|
|
Duration of Morning Stiffness at Month 12
Ramy czasowe: Month 12
|
Duration of morning stiffness: Time elapsed when participant woke up in morning and was able to resume normal activities without stiffness in minutes.
Increase in stiffness duration from baseline represented disease progression and/or joint worsening, no change represented halting of disease progression, and a decrease represented improvement.
|
Month 12
|
|
Health Assessment Questionnaire (HAQ) at Month 6
Ramy czasowe: Month 6
|
HAQ: participant-reported assessment of ability to perform tasks in 8 categories of daily living activities: dress/groom; arise; eat; walk; reach; grip; hygiene; and common activities over past week.
Each item scored on 4-point scale from 0 to 3: 0=no difficulty; 1=some difficulty; 2=much difficulty; 3=unable to do.
Overall score was computed as the sum of domain scores and divided by the number of domains answered.
Total possible score range 0-3 where 0 = least difficulty and 3 = extreme difficulty.
|
Month 6
|
|
Health Assessment Questionnaire (HAQ) at Month 12
Ramy czasowe: Month 12
|
HAQ: participant-reported assessment of ability to perform tasks in 8 categories of daily living activities: dress/groom; arise; eat; walk; reach; grip; hygiene; and common activities over past week.
Each item scored on 4-point scale from 0 to 3: 0=no difficulty; 1=some difficulty; 2=much difficulty; 3=unable to do.
Overall score was computed as the sum of domain scores and divided by the number of domains answered.
Total possible score range 0-3 where 0 = least difficulty and 3 = extreme difficulty.
|
Month 12
|
|
Recent-Onset Arthritis Disability (ROAD) at Month 6
Ramy czasowe: Month 6
|
ROAD questionnaire: valid and responsive tool for measuring functional ability in RA participants.
Consists of 12-items related to fine movements of upper extremity, locomotor activities of lower extremity, and activities that involve both upper and lower extremities.
For each item participant rated the level of difficulty over the past week on a 5-point scale ranging from 0 (without any difficulty) to 4 (unable to do).
Total ROAD score were transformed to a 0 to 10 point scale, where 0 = best status and 10 = poorest status.
|
Month 6
|
|
Recent-Onset Arthritis Disability (ROAD) at Month 12
Ramy czasowe: Month 12
|
ROAD questionnaire: valid and responsive tool for measuring functional ability in RA participants.
Consists of 12-items related to fine movements of upper extremity, locomotor activities of lower extremity, and activities that involve both upper and lower extremities.
For each item participant rated the level of difficulty over the past week on a 5-point scale ranging from 0 (without any difficulty) to 4 (unable to do).
Total ROAD score were transformed to a 0 to 10 point scale, where 0 = best status and 10 = poorest status.
|
Month 12
|
|
Radiological Assessment of Hands and Feet Based on Sharp-van Der Hejde (SvH) Scoring Method at Month 6
Ramy czasowe: Month 6
|
SvH method included 16 areas for erosions and 15 areas for joint space narrowing (JSN) and subluxation/luxation in each hand, 6 areas for erosions and 6 areas for JSN and subluxation/luxation in each foot.
Erosion per joint scored on 0-5 point scale; 0=normal joint to 5=complete collapse.
Total erosion score for hands:0-160, for feet:0-120.
JSN and subluxation/luxation scored on 0-4 point scale; 0=normal joint to 4= a bony ankylosis/a complete luxation of joint.
Total JSN and subluxation/luxation score for hands:0-120, for feet:0-48.
Total SvH score = 0-448; higher score=more erosion and JSN.
|
Month 6
|
|
Radiological Assessment of Hands and Feet Based on Sharp-Van Der Hejde (SvH) Scoring Method at Month 12
Ramy czasowe: Month 12
|
SvH method included 16 areas for erosions and 15 areas for JSN and subluxation/luxation in each hand, 6 areas for erosions and 6 areas for JSN and subluxation/luxation in each foot.
Erosion per joint scored on 0-5 point scale; 0=normal joint to 5=complete collapse.
Total erosion score for hands:0-160, for feet:0-120.
JSN and subluxation/luxation scored on 0-4 point scale; 0=normal joint to 4= a bony ankylosis/a complete luxation of joint.
Total JSN and subluxation/luxation score for hands:0-120, for feet:0-48.
Total SvH score = 0-448; higher score=more erosion and JSN.
|
Month 12
|
Współpracownicy i badacze
Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.
Sponsor
Publikacje i pomocne linki
Osoba odpowiedzialna za wprowadzenie informacji o badaniu dobrowolnie udostępnia te publikacje. Mogą one dotyczyć wszystkiego, co jest związane z badaniem.
Daty zapisu na studia
Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.
Główne daty studiów
Rozpoczęcie studiów
1 stycznia 2008
Zakończenie podstawowe (Rzeczywisty)
1 czerwca 2010
Ukończenie studiów (Rzeczywisty)
1 czerwca 2010
Daty rejestracji na studia
Pierwszy przesłany
17 listopada 2008
Pierwszy przesłany, który spełnia kryteria kontroli jakości
18 listopada 2008
Pierwszy wysłany (Oszacować)
19 listopada 2008
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Oszacować)
4 lutego 2013
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
31 grudnia 2012
Ostatnia weryfikacja
1 grudnia 2012
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- 0881A1-102317
- 0881A-102317 ; B1801118
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .
Badania kliniczne na As per routinary clinical care
-
Jung Min KooNieznanyKlatka piersiowa lejkowataRepublika Korei
-
University of NottinghamEnhanced Recovery After Surgery Group (part of ESPEN)Zakończony
-
Evidence-Based Practice Institute, Seattle, WAZakończonyDepresja | Bezsenność | SamobójstwoStany Zjednoczone
-
Johnson & Johnson Consumer Inc. (J&JCI)Zakończony