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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
Asahi Kasei Medical Co., Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ulcerative Colitis focused on measuring Cellsorba EX

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
July 27, 2009
Last Updated
December 5, 2012
Sponsor
Asahi Kasei Medical Co., Ltd.
Collaborators
Asahi Kasei Medical Europe GmbH
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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

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A Study of Leukocytapheresis (LCAP) in Patients With Ulcerative Colitis (UC)

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