Ignite Creation Date:
2024-05-05 @ 12:10 PM
Last Modification Date:
2024-10-26 @ 9:21 AM
Study NCT ID:
NCT00264095
Status:
COMPLETED
Last Update Posted:
2014-04-28
First Post:
2005-12-09
Brief Title:
An Observational Study of Blood Management Techniques in Oncology Surgical Treatment
Sponsor:
Janssen-Cilag BV
Organization:
Janssen-Cilag BV
Study Overview
Official Title:
Blood Management Observation in Oncology Surgical Treatment BOOST
Status:
COMPLETED
Status Verified Date:
2014-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is to observe the methods used to manage blood loss in surgical procedures to remove tumors from patients with cancer and to determine if there is a relationship with the need for blood transfusions
Detailed Description:
Considerable blood loss typically accompanies surgical procedures to remove malignant tumors Blood transfusions the best method of compensating for blood loss during surgery have associated medical risks including infection transmission and allergic reaction in addition to using significant amounts of red blood cells which are often in short supply Options exist to manage blood loss before surgery including a procedure where a patients own blood is stored in advance to be given if needed during surgery and drug intervention where a drug is given before surgery to help increase red blood cell production thereby maintaining hemoglobin and oxygen levels in the body during surgery This is a multi-center observational study to collect information regarding the methods used to manage blood loss in patients undergoing surgical removal of malignant tumors in the Netherlands Information will be collected by study center and by patient over the course of approximately 18 months For study center information each observation period will last 2 months and there will be at least a 2-month interval between each observation period For patient information there is one continuous observation period General information regarding the frequency of use of different blood-saving techniques for the various types of operations performed will be collected from each of the centers participating in the study Data obtained at the onset of the study will be compared to follow-up data gathered throughout the additional reporting periods and trends or changes in frequency of use of blood-saving techniques will be noted The following information will be collected medical history tumor stage typesite of operation anticipated vs actual blood loss during surgery most recent hemoglobin and hematocrit values prior to the operation blood-saving techniques used and the number of units and types of blood transfusions up to 24 hours after the operation Information will be obtained from patients medical records No medication will be supplied by the study Sponsor and no specific procedures will be required for the study Each patients surgeon and anesthesiologist will be responsible for all decisions regarding hisher care and treatment during the operation Information may be collected a maximum of one time from each patient during this study and there will be no follow-up information collected from individual patients Since the study involves only the collection of information no treatment will be required by the Sponsor and no medication will be supplied by the Sponsor
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| EPOSUR4001 | None | None | None |