- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT00898482
Collecting and Storing Samples of Blood From Patients With Pancreatic Cancer and Healthy Participants
Pancreatic Cancer Serum and Peripheral Blood Lymphocyte Repository
RATIONALE: Collecting and storing samples of blood from patients with cancer and healthy participants to test in the laboratory may help the study of cancer in the future.
PURPOSE: This study is collecting and storing samples of blood from patients with pancreatic cancer and healthy participants.
Studieöversikt
Status
Betingelser
Detaljerad beskrivning
OBJECTIVES:
- Establish a central pancreatic cancer specimen (including serum and peripheral blood lymphocytes) repository to serve as a resource for current or future scientific studies.
- Utilize the clinical database to perform clinicopathologic correlation with the results of those studies.
- Test new hypotheses as they emerge.
OUTLINE: This is a prospective study.
Blood is collected from patients with pancreatic cancer at baseline and then every 3-6 months for up to 2 years. All other participants have blood collected at baseline and complete questionnaires at baseline and then every 3-6 months for up to 2 years. Serum and peripheral blood lymphocytes obtained from the blood samples are frozen and stored.
PROJECTED ACCRUAL: A total of 200 patients and 200 other participants will be accrued for this study.
Studietyp
Inskrivning (Faktisk)
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Testmetod
Studera befolkning
Beskrivning
DISEASE CHARACTERISTICS:
Meets 1 of the following criteria:
- Histologically confirmed pancreatic malignant neoplasm
- Serologically or image-confirmed diagnosis of pancreatitis or nonmalignant pancreatic disease
Healthy, at-risk participant meeting the following criteria:
- Smoker, diabetic, and/or has a family history of pancreatic cancer
- Healthy participant (no history of cancer)
PATIENT CHARACTERISTICS:
- Not specified
PRIOR CONCURRENT THERAPY:
- Not specified
Studieplan
Hur är studien utformad?
Designdetaljer
- Observationsmodeller: Endast fall
Kohorter och interventioner
Grupp / Kohort |
Intervention / Behandling |
|---|---|
|
Friska individer
|
This is a non-intervention study.
Non-intervention study.
|
|
At risk individuals
|
This is a non-intervention study.
Non-intervention study.
|
|
Cancer patients
|
This is a non-intervention study.
Non-intervention study.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Tidsram |
|---|---|
|
Establishment of a central pancreatic cancer specimen repository
Tidsram: No time frame
|
No time frame
|
|
Utilization of the clinical database to perform clinicopathologic correlation with the results of current or future scientific studies
Tidsram: No time frame
|
No time frame
|
|
Test new hypotheses as they emerge
Tidsram: No time frame
|
No time frame
|
Samarbetspartners och utredare
Samarbetspartners
Utredare
- Studiestol: Daniel A. Laheru, MD, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Studieavstämningsdatum
Studera stora datum
Studiestart
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- JHOC-J0533 CDR0000452792
- P30CA006973 (U.S.S. NIH-anslag/kontrakt)
- JHOC-J0533
- JHOC-05042601
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