- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT00735943
Macugen Observational Study
Studienübersicht
Status
Intervention / Behandlung
Detaillierte Beschreibung
To be eligible for enrollment in this study, patients must receive the first injection of Macugen intravitreal in at least one eye for treatment of wet age-related macular degeneration (AMD). The decision to prescribe Macugen will necessarily precede and will be independent of the decision to enroll patient into the study.
If both eyes of a patient receive injection Macugen, only one eye will be included in the study. If both eyes receive first injection Macugen after initiation of the study, only the first treated eye will be included in the analysis. If one eye has already received Macugen when the study starts and the second eye receives injection after the study initiation, the second eye will be included in the analysis.
The study was prematurely discontinued due to delay in meeting pre-defined protocol recruitment milestones on August 30, 2010. There were no safety concerns regarding the study in the decision to terminate the trial.
Studientyp
Einschreibung (Tatsächlich)
Kontakte und Standorte
Studienorte
-
-
Gujarat
-
Navrangpura, Ahemdabad, Gujarat, Indien, 380009
- Pfizer Investigational Site
-
-
Haryana
-
Gurgaon, Haryana, Indien, 122 002
- Pfizer Investigational Site
-
-
Kerala
-
Cochin, Kerala, Indien, 682 015
- Pfizer Investigational Site
-
-
Maharashtra
-
Mumbai, Maharashtra, Indien, 400 054
- Pfizer Investigational Site
-
-
Rajasthan
-
Jaipur, Rajasthan, Indien, 302 004
- Pfizer Investigational Site
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Probenahmeverfahren
Studienpopulation
Beschreibung
Inclusion Criteria:
- To be eligible for enrollment in this study, patients must receive the first injection of Macugen intravitreal in at least one eye for treatment of wet age-related macular degeneration (AMD).
Exclusion Criteria:
- Active or suspected ocular or periocular infection.
- Known hypersensitivity to pegaptanib sodium or any other excipient in this product.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
Percentage of Participants Showing Stabilization, Improvement or Deterioration of Visual Acuity (VA)
Zeitfenster: Baseline through 12 months or last follow-up visit before study termination
|
VA was measured using ETDRS (Early Treatment Diabetic Retinopathy Study) chart at 4 meter distance, at 1 meter distance (if participant's VA was poor) or verifying if the participant was able only to count fingers, to perceive hand motion or light.
VA was assessed as the number of ETDRS letters correctly read.
VA statuses were defined as: Stabilization: loss of less than 15 letters in the best corrected VA (BCVA); Improvement: gain of more than or equal to 15 letters in the BCVA; Deterioration: loss of more than or equal to 15 letters in the BCVA.
|
Baseline through 12 months or last follow-up visit before study termination
|
Average Number of Injections to Achieve Stabilization of VA
Zeitfenster: 12 months or last follow-up visit before study termination
|
Stabilization of VA was defined as loss of less than 15 letters in the BCVA.
For each participant, number of injections before reaching the first "stabilization in VA" (considered as an event) was counted.
For participant having no event, the time to the number of injections to reach an event was unobserved at the number of injections before the last follow up.
|
12 months or last follow-up visit before study termination
|
Median Number of Injections to Achieve Stabilization of VA
Zeitfenster: 12 months or last follow-up visit before study termination
|
Stabilization of VA was defined as loss of less than 15 letters in the BCVA.
Median number of injections to achieve stabilization of VA was estimated via the Kaplan Meier method.
For each participant, number of injections before reaching the first "stabilization in VA" (considered as an event) was counted.
For participant having no event, the time to the number of injections to reach an event was unobserved at the number of injections before the last follow up.
|
12 months or last follow-up visit before study termination
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
Percentage of Participants Receiving Macugen Monotherapy Versus Those Receiving a Combination Therapy
Zeitfenster: 12 months or last follow-up visit before study termination
|
Macugen monotherapy: referred to participants receiving Macugen in the study eye during the study that is (i.e.) participants without any concomitant drug treatment or nondrug treatment for the study eye during the study.
Combination therapy: referred to participants receiving combination therapy in the study eye (during the study) i.e. participants with any concomitant drug treatment or nondrug treatment for the study eye during the study.
|
12 months or last follow-up visit before study termination
|
Percentage of Participants Showing Improvement in Optical Coherence Tomography (OCT) Parameters
Zeitfenster: 12 months or last follow-up visit before study termination
|
OCT, a noninvasive, noncontact, transpupillary imaging technology, was utilized to image retinal structures in vivo with a resolution of 10 to 17 microns.
The anatomic layers within the retina, retinal thickness could be measured.
Improvement in OCT parameters was defined as a reduction of more than or equal to 100 microns in the central macular thickness (Center subfield).
|
12 months or last follow-up visit before study termination
|
Percentage of Participants Showing Improvement in Fundus Fluorescein Angiography (FFA) Parameters
Zeitfenster: 12 months or last follow-up visit before study termination
|
A fluorescein angiogram provides information about the condition of the retina.
Improvement in FFA parameters was defined as absence of progression of the lesion or decrease in the size of the lesion and absence of new lesions on FFA i.e. change in lesion size from baseline must be less than or equal to 0 disc area(DA) and no new lesions.
|
12 months or last follow-up visit before study termination
|
Percentage of Participants With Early Lesions Showing Stabilization and Improvement of VA
Zeitfenster: 12 months or last follow-up visit before study termination
|
Early lesions were defined by any 2 of the following criteria: occult lesion diagnosed on FFA; baseline VA of more than or equal to 54 ETDRS letters; lesion size of less than 2DA on FFA.
Stabilization of VA was defined as loss of less than 15 letters in the BCVA.
Improvement in the VA was defined as gain of more than or equal to 15 letters in the BCVA.
|
12 months or last follow-up visit before study termination
|
Average Number of Injections to Achieve Stabilization of VA in Participants With Early Lesions
Zeitfenster: 12 months or last follow-up visit before study termination
|
Stabilization of VA was defined as loss of less than 15 letters in the BCVA.
For each participant, number of injections before reaching the first "stabilization in VA" (considered as an event) was counted.
For participant having no event, the time to the number of injections to reach an event was unobserved at the number of injections before the last follow up.
|
12 months or last follow-up visit before study termination
|
Median Number of Injections to Achieve Stabilization of VA in Participants With Early Lesions
Zeitfenster: 12 months or last follow-up visit before study termination
|
Stabilization of VA was defined as loss of less than 15 letters in the BCVA.
Median number of injections to achieve stabilization of VA in participants with early lesions was estimated via the Kaplan Meier method.
For each participant, number of injections before reaching the first "stabilization in VA" (considered as an event) was counted.
For participant having no event, the time to the number of injections to reach an event was unobserved at the number of injections before the last follow up.
|
12 months or last follow-up visit before study termination
|
Percentage of Participants With Occult or Minimally Classic and Classic Lesions Showing Stabilization and Improvement in VA
Zeitfenster: 12 months or last follow-up visit before study termination
|
FFA was utilized to characterize the lesions as follows: Classic lesion: more than 50% of the lesion had a well-demarcated area of hyperfluorescence; minimally classic lesion: less than or equal to 50% of lesion had well-demarcated area of hyperfluorescence; occult lesion: lesion with no well demarcated borders.
VA statuses were defined as: stabilization: loss of less than 15 letters in the BCVA; improvement: gain of more than or equal to 15 letters in the BCVA.
|
12 months or last follow-up visit before study termination
|
Percentage of Participants Who Were Treatment Naive When Started on Macugen Versus Those Previously Treated by Any Other Therapy Except Macugen
Zeitfenster: 12 months or last follow-up visit before study termination
|
Participants were considered treatment naive when started on Macugen and without any previous drug or non drug treatment administered to the study eye.
Participants were considered previously treated by any other therapy if received any other drug or non drug treatment to the study eye except Macugen.
|
12 months or last follow-up visit before study termination
|
Percentage of Participants Showing Stabilization or Improvement in VA in the Subgroup Previously Treated by Other Therapy
Zeitfenster: 12 months or last follow-up visit before study termination
|
VA was measured using ETDRS chart at 4 meter distance, at 1 meter distance (if patient's VA was poor) or verifying if the patient was able only to count fingers, to perceive hand motion or light.
VA was measured as the number of ETDRS letters correctly read.
VA statuses were defined as: stabilization: loss of less than 15 letters in the BCVA; improvement: gain of more than 15 letters in the BCVA.
|
12 months or last follow-up visit before study termination
|
Percentage of Participants Showing Improvement in OCT in the Subgroup Previously Treated by Other Therapy
Zeitfenster: 12 months or last follow-up visit before study termination
|
OCT, a noninvasive, noncontact, transpupillary imaging technology, was utilized to image retinal structures in vivo with a resolution of 10 to 17 microns.
The anatomic layers within the retina, retinal thickness could be measured.
Improvement in OCT parameters was defined as a reduction of more than or equal to 100 microns in the central macular thickness (Center subfield).
Improvement in OCT parameters was measured based on this single parameter.
|
12 months or last follow-up visit before study termination
|
Percentage of Participants Showing Improvement in OCT in the Subgroup Which Were Not Treatment Naive
Zeitfenster: 12 months or last follow-up visit before study termination
|
OCT, a noninvasive, noncontact, transpupillary imaging technology, was utilized to image retinal structures in vivo with a resolution of 10 to 17 microns.
The anatomic layers within the retina, retinal thickness could be measured.
Improvement in OCT parameters was defined as a reduction of more than or equal to 100 microns in the central macular thickness (Center subfield).
Improvement in OCT parameters was measured based on this single parameter.
|
12 months or last follow-up visit before study termination
|
Mitarbeiter und Ermittler
Sponsor
Publikationen und hilfreiche Links
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Schätzen)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- A5751031
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 .
Klinische Studien zur Makuladegeneration
-
University of Missouri-ColumbiaZurückgezogenDegeneration der Lendenwirbelsäule | Degeneration der HalswirbelsäuleVereinigte Staaten
-
Muğla Sıtkı Koçman UniversityAbgeschlossenMeniskus; DegenerationTruthahn
-
NanoFUSE Biologics, LLCUnbekanntKnochen; Degeneration
-
Institut Straumann AGAbgeschlossenDegeneration; KnochenDeutschland, Ungarn, Belgien, Italien, Spanien, Schweden, Schweiz
-
Technical University of MunichNoch keine RekrutierungDegeneration der Wirbelsäule
-
University Hospital, Basel, SwitzerlandSwiss National Science FoundationAktiv, nicht rekrutierendDegeneration des GelenkknorpelsSchweiz
-
ElsanAbgeschlossenDegeneration der LendenwirbelsäuleFrankreich
-
Orthofix Inc.AbgeschlossenDegeneration der LendenwirbelsäuleVereinigte Staaten
-
Snyder, Robert W., M.D., Ph.D., P.C.Snyder Biomedical CorporationAbgeschlossenRetina | Makula; DegenerationVereinigte Staaten
-
The Methodist Hospital Research InstituteRekrutierung
Klinische Studien zur Kein Eingriff
-
RTI InternationalNo Means No WorldwideAbgeschlossenSexuelle Gewalt | Geschlechtsspezifische GewaltSüdafrika
-
University of Illinois at ChicagoUniversity of Chicago; The Broad FoundationAbgeschlossenColitis ulcerosaVereinigte Staaten
-
King's College LondonMedical University of Graz; Radboud University Medical Center; Novo Nordisk A/S; Juvenile Diabetes Research Foundation und andere MitarbeiterAbgeschlossenDiabetes mellitus, Typ 2 | Hypoglykämie | Diabetes mellitus, Typ 1 | Hypoglykämie-WahrnehmungsstörungVereinigtes Königreich
-
Otsuka Pharmaceutical Factory, Inc.CelerionAbgeschlossen
-
Universitat Jaume IAbgeschlossen
-
Seoul National University HospitalSamsung Medical Center; Chosun University HospitalBeendetRadiofrequenz-Ablation | Mikrowellen-AblationKorea, Republik von
-
University of MinnesotaAbgeschlossen
-
University of ValenciaHospital de la RiberaUnbekannt
-
China National Center for Cardiovascular DiseasesUnbekannt
-
Catharina Ziekenhuis EindhovenAbgeschlossen