Effect of Human Thrombin With Gelatin Matrix on Perioperative Blood Loss in Scoliosis Surgery
Primary Purpose
Adolescent Idiopathic Scoliosis
Status
Completed
Phase
Phase 4
Locations
Finland
Study Type
Interventional
Intervention
Gelatin matrix with human derived thrombin (Floseal, Baxter)
Sponsored by
About this trial
This is an interventional treatment trial for Adolescent Idiopathic Scoliosis focused on measuring RCT, Gelatin matrix, thrombin, idiopathic scoliosis, Surgery
Eligibility Criteria
Inclusion Criteria:
- Patients will be included if between 10 and 20 years of age, no contraindication for Floseal use, posterior scoliosis surgery using total pedicle screw technique for AIS with normal blood coagulation and normal whole spine magnetic resonance images except spinal deformity (AIS).
Exclusion Criteria:
- Need for anteroposterior surgery
- Need for vertebral column resection
- Smoking
- Diabetes mellitus
- Abnormalities in blood coagulation
Sites / Locations
- Helsinki University Central Hospital
- Tampere University Central Hospital
- Turku Children's Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Conventional group
Floseal
Arm Description
conventional blood saving methods (use of bone wax for cancellous bony bleeding; bipolar diathermy and epidural space packing for epidural venous bleeding)
Gelatin matrix with human derived thrombin (Floseal) used in adolescents undergoing posterior spinal deformity surgery for adolescent idiopathic scoliosis (AIS)
Outcomes
Primary Outcome Measures
Total perioperative blood loss
Total blood loss during surgery + drain output, millilitres
Secondary Outcome Measures
Used blood products
Red cell, frozen plasma, and thrombocyte units
Blood loss during surgery
Blood loss during primary surgery, in millilitres
Time of surgery
Time of surgery (hours, minutes)
Full Information
NCT ID
NCT01451788
First Posted
September 30, 2011
Last Updated
October 5, 2020
Sponsor
Turku University Hospital
Collaborators
Tampere University Hospital, Helsinki University Central Hospital
1. Study Identification
Unique Protocol Identification Number
NCT01451788
Brief Title
Effect of Human Thrombin With Gelatin Matrix on Perioperative Blood Loss in Scoliosis Surgery
Official Title
Effectiveness Of Gelatin Matrix With Human Derived Thrombin On Blood Loss, Surgical Time, Hospital Stay And Complications In Adolescents Undergoing Spine Surgery For Adolescent Idiopathic Scoliosis: A Randomized Clinical Trial.
Study Type
Interventional
2. Study Status
Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
November 2011 (Actual)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
December 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Turku University Hospital
Collaborators
Tampere University Hospital, Helsinki University Central Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The Finnish Paediatric Orthopaedic Study Group will perform a prospective randomized, multicenter, clinical trial comparing Gelatin matrix with human derived thrombin (Floseal, Baxter) and without use of Floseal in adolescents undergoing posterior spinal deformity surgery for AIS (adolescent idiopathic scoliosis between 45 and 90 degrees) in Turku, Tampare and Helsinki Children's Hospitals. Sixty patients will be randomized into the intervention group receiving Floseal (n=30) and control group not receiving Floseal (n=30). Each University Hospital will treat 10 Floseal and 10 conventional treated scoliosis patients (block randomization). Both treatment groups will be allowed to use conventional blood saving methods.
Detailed Description
Background: Posterior spinal deformity surgery can be associated with major blood loss, especially from cancellous bone or epidural venous plexus. Products such as Gelatin Matrix with bovine derived thrombin (Floseal) can be used to prevent blood loss in adult patients undergoing spine surgery.
Aim: To document and compare effectiveness of Gelatin matrix with human derived thrombin with conventional blood loss control methods in adolescents undergoing posterior spinal deformity surgery for adolescent idiopathic scoliosis (AIS), who do not need vertebral column resection.
Methods: The Finnish Paediatric Orthopaedic Study Group will perform a prospective randomized, multicenter, clinical trial comparing Gelatin matrix with human derived thrombin (Floseal, Baxter) and without use of Floseal in adolescents undergoing posterior spinal deformity surgery for AIS (adolescent idiopathic scoliosis between 45 and 90 degrees) in Turku, Tampere and Helsinki Children's Hospitals. Sixty patients will be randomized into the intervention group receiving Floseal (n=30) and control group not receiving Floseal (n=30). Each University Hospital will treat 10 Floseal and 10 conventional treated scoliosis patients (block randomization). Both treatment groups will be allowed to use conventional blood saving methods.
Main outcome measures:
Blood loss during surgery (millilitres) Drain output during 24 hours (millilitres) Total blood loss (Blood loss during surgery + drain output, millitres) Used blood products (Red cell, frozen plasma, and thrombocyte units) Time of surgery Hospital stay Cost benefit analysis (blood product use, surgical time, hospital stay) Complications related to use of Floseal as a secondary outcome measure.
Primary Hypothesis and expected outcomes: Use of Floseal will reduce blood loss and surgical time in patients undergoing spine surgery for adolescent idiopathic scoliosis (Level-I evidence). Cost benefit analysis will most probably show that the use of Floseal is cost effective. E.g. the value of one allogenic Red Blood Cell unit is 400€. If no red blood cell units are needed instead of the usual three, the reduced blood product use alone will cover the extra costs of Floseal use. In addition, if no allogenic blood infusions are needed, the risk of infections will probably be significantly less. Reduced surgical time and shorter hospital stay may also be cost reducing findings in patients receiving Floseal.
Safety Aspects: Gelatin Matrix with human derived thrombin (Floseal, Baxter Biosurgery) is indicated for blood loss control in patients undergoing spine surgery when other methods are less effective.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adolescent Idiopathic Scoliosis
Keywords
RCT, Gelatin matrix, thrombin, idiopathic scoliosis, Surgery
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Conventional group
Arm Type
No Intervention
Arm Description
conventional blood saving methods (use of bone wax for cancellous bony bleeding; bipolar diathermy and epidural space packing for epidural venous bleeding)
Arm Title
Floseal
Arm Type
Experimental
Arm Description
Gelatin matrix with human derived thrombin (Floseal) used in adolescents undergoing posterior spinal deformity surgery for adolescent idiopathic scoliosis (AIS)
Intervention Type
Device
Intervention Name(s)
Gelatin matrix with human derived thrombin (Floseal, Baxter)
Other Intervention Name(s)
Floseal, Baxter
Intervention Description
Floseal will be used to stop cancellous bone bleeding, pedicle channel bleeding or epidural space bleeding by injecting suitable amount of this matrix and irrigating it away after few minutes.
Primary Outcome Measure Information:
Title
Total perioperative blood loss
Description
Total blood loss during surgery + drain output, millilitres
Time Frame
Surgery time (up to 8 hours) + first postoperative 24 hours
Secondary Outcome Measure Information:
Title
Used blood products
Description
Red cell, frozen plasma, and thrombocyte units
Time Frame
Surgery time (up to 8 hours) + first 24 hours postoperatively
Title
Blood loss during surgery
Description
Blood loss during primary surgery, in millilitres
Time Frame
up to 8 hours
Title
Time of surgery
Description
Time of surgery (hours, minutes)
Time Frame
up to 8 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients will be included if between 10 and 20 years of age, no contraindication for Floseal use, posterior scoliosis surgery using total pedicle screw technique for AIS with normal blood coagulation and normal whole spine magnetic resonance images except spinal deformity (AIS).
Exclusion Criteria:
Need for anteroposterior surgery
Need for vertebral column resection
Smoking
Diabetes mellitus
Abnormalities in blood coagulation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ilkka J. Helenius, M.D., Ph.D.
Organizational Affiliation
Turku Children's Hospital, Turku University Central Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Helsinki University Central Hospital
City
Helsinki
Country
Finland
Facility Name
Tampere University Central Hospital
City
Tampere
Country
Finland
Facility Name
Turku Children's Hospital
City
Turku
ZIP/Postal Code
FI-20521
Country
Finland
12. IPD Sharing Statement
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Effect of Human Thrombin With Gelatin Matrix on Perioperative Blood Loss in Scoliosis Surgery
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