A Study of Leukocytapheresis (LCAP) in Patients With Ulcerative Colitis (UC)
Primary Purpose
Ulcerative Colitis
Status
Terminated
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
Cellsorba EX
Sponsored by
About this trial
This is an interventional treatment trial for Ulcerative Colitis focused on measuring Cellsorba EX
Eligibility Criteria
Inclusion Criteria:
- Patients diagnosed to have UC in the active stage based on clinical symptoms and findings from endoscopy
- Patients with pancolitis type or left-sided colitis type lesion of 15 cm or longer observed endoscopically
- Patients with Mayo score between 5 and 10
- Patients with Mayo sub-score (findings from flexible sigmoidoscopy) of 2 or 3
- Patients not having received any corticosteroids (referred to as steroids) (p.o., i.v., enema, suppository) within the past 6 weeks
Exclusion Criteria:
- Patients with a difficulty in peripheral vascular access
- Patients having received ACE inhibitor (at least 10 times of its half-life time for interval needed before initiating the treatment)
- Patients with toxic megacolon
- Patients with a malignant disease or its experience
- Patients with a severe cardiovascular disease (grade III or IV by the Classification of heart functions of the New York Heart Association (NYHA))
- Patients with a liver or kidney disease (AST(GOT) or ALT(GPT) or total bilirubin or creatinine level which is 2 or more times higher than the upper limit of normal (abbreviated as ULN, hereinafter)
- Patients suspected to have or having HBV or HCV or HIV or pathogenic bacteria
- Patients on anticoagulant therapy or with abnormality in the blood coagulation system (PT or PTT levels which are 1.5 or more times higher than ULN
- Pregnant women or patients with possible pregnancy
- Breast feeding women
- Patients weighing 40 kg or less
- Patients with hemoglobin level of less than 6.5 mmol/L (10.5 g/dL)
- Patients with platelet count of less than 150 x 103/mm3, 150 x 109/L (15 x 104/mm3)
- Patients with white blood cell count of less than 3.5 x 109/L (3,500/mm3)
- Patients with hypotension (with systolic blood pressure of 80 mmHg or less)
Sites / Locations
- Tel Aviv Sourasky Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Sham Comparator
Arm Label
Cellsorba EX
Sham treatment
Arm Description
Outcomes
Primary Outcome Measures
Clinical response
Secondary Outcome Measures
Remission, Mayo scores, Mucosal healing, CRP
Full Information
NCT ID
NCT00947674
First Posted
July 27, 2009
Last Updated
December 5, 2012
Sponsor
Asahi Kasei Medical Co., Ltd.
Collaborators
Asahi Kasei Medical Europe GmbH
1. Study Identification
Unique Protocol Identification Number
NCT00947674
Brief Title
A Study of Leukocytapheresis (LCAP) in Patients With Ulcerative Colitis (UC)
Official Title
Prospective, Randomized, Double-Blind, Sham Treatment Controlled Multicenter Study to Evaluate Efficacy and Safety of Cellsorba™EX Used for Leukocytapheresis (LCAP) in Patients With Steroid-Free, Active Ulcerative Colitis
Study Type
Interventional
2. Study Status
Record Verification Date
December 2012
Overall Recruitment Status
Terminated
Why Stopped
short of enrollment
Study Start Date
May 2009 (undefined)
Primary Completion Date
January 2012 (Actual)
Study Completion Date
October 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Asahi Kasei Medical Co., Ltd.
Collaborators
Asahi Kasei Medical Europe GmbH
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a prospective, randomized, double-blind, sham treatment controlled multicenter study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ulcerative Colitis
Keywords
Cellsorba EX
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
52 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Cellsorba EX
Arm Type
Experimental
Arm Title
Sham treatment
Arm Type
Sham Comparator
Intervention Type
Device
Intervention Name(s)
Cellsorba EX
Intervention Description
conduct treatment twice a week for 3 weeks and once a week for 4 weeks, total 10 times
Primary Outcome Measure Information:
Title
Clinical response
Time Frame
at 8th week
Secondary Outcome Measure Information:
Title
Remission, Mayo scores, Mucosal healing, CRP
Time Frame
at 8th and 16th week
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients diagnosed to have UC in the active stage based on clinical symptoms and findings from endoscopy
Patients with pancolitis type or left-sided colitis type lesion of 15 cm or longer observed endoscopically
Patients with Mayo score between 5 and 10
Patients with Mayo sub-score (findings from flexible sigmoidoscopy) of 2 or 3
Patients not having received any corticosteroids (referred to as steroids) (p.o., i.v., enema, suppository) within the past 6 weeks
Exclusion Criteria:
Patients with a difficulty in peripheral vascular access
Patients having received ACE inhibitor (at least 10 times of its half-life time for interval needed before initiating the treatment)
Patients with toxic megacolon
Patients with a malignant disease or its experience
Patients with a severe cardiovascular disease (grade III or IV by the Classification of heart functions of the New York Heart Association (NYHA))
Patients with a liver or kidney disease (AST(GOT) or ALT(GPT) or total bilirubin or creatinine level which is 2 or more times higher than the upper limit of normal (abbreviated as ULN, hereinafter)
Patients suspected to have or having HBV or HCV or HIV or pathogenic bacteria
Patients on anticoagulant therapy or with abnormality in the blood coagulation system (PT or PTT levels which are 1.5 or more times higher than ULN
Pregnant women or patients with possible pregnancy
Breast feeding women
Patients weighing 40 kg or less
Patients with hemoglobin level of less than 6.5 mmol/L (10.5 g/dL)
Patients with platelet count of less than 150 x 103/mm3, 150 x 109/L (15 x 104/mm3)
Patients with white blood cell count of less than 3.5 x 109/L (3,500/mm3)
Patients with hypotension (with systolic blood pressure of 80 mmHg or less)
Facility Information:
City
Praha
Country
Czech Republic
City
Hannover
Country
Germany
City
Rostock
Country
Germany
Facility Name
Tel Aviv Sourasky Medical Center
City
Tel Aviv
Country
Israel
City
Hyogo
Country
Japan
City
Tokyo
Country
Japan
City
Gothenburg
Country
Sweden
City
Stockholm
Country
Sweden
City
Oxford
Country
United Kingdom
City
Southampton
Country
United Kingdom
12. IPD Sharing Statement
Learn more about this trial
A Study of Leukocytapheresis (LCAP) in Patients With Ulcerative Colitis (UC)
We'll reach out to this number within 24 hrs