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Anti-Tumor Necrosis Factor Therapy In Patients With Ankylosing Spondylitis

Primary Purpose

Ankylosing Spondylitis

Status
Unknown status
Phase
Phase 2
Locations
Taiwan
Study Type
Interventional
Intervention
TNF alpha
NSAIDs and sulfasalazine
Sponsored by
Chung Shan Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ankylosing Spondylitis focused on measuring Adalimumab, NSAIDs, safety, efficacy

Eligibility Criteria

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

Inclusion Criteria:

  • Age ≥18 years old
  • HLA B27 positive
  • X ray examination
  • Clinical symptoms and physical examination, the following three conditions are subject to at least two:

    i.lower back pain and morning stiffness symptoms persist more than 3 months ii. lumbar activity is restricted iii. chest expansion is restricted

  • Active disease for four weeks or more (continue two examination BASDAI>6, ESR> 28 mm/1 hr and CRP>1 mg/dl)

Exclusion Criteria:

  • pregnant or breast-feeding women
  • patients with active infections
  • highly infectious patients
  • Cancer or precancerous condition of the patient
  • multiple sclerosis

Sites / Locations

  • Chung Shan Medical University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

NSAIDs(+) and sulfasalazine(+)

NSAIDs(+) and sulfasalazine(-)

NSAIDs(-) and sulfasalazine(+)

NSAIDs(-) and sulfasalazine(-)

Arm Description

use TNF alpha: Adalimumab (Humira)、Etanercept (Enbrel) or Golimumab (Simponi) combine with use of NSAIDs and no sulfasalazine

use TNF alpha: Adalimumab (Humira)、Etanercept (Enbrel) or Golimumab (Simponi) combine with use of NSAIDs and no sulfasalazine

use TNF alpha: Adalimumab (Humira)、Etanercept (Enbrel) or Golimumab (Simponi) combine with use of sulfasalazine and no NSAIDs

use TNF alpha: Adalimumab (Humira)、Etanercept (Enbrel) or Golimumab (Simponi) neither NSAIDs nor sulfasalazine

Outcomes

Primary Outcome Measures

mSASSS (Modified Stoke Ankylosing Spondylitis Spinal Score)
weeks 92 of the spinal injury

Secondary Outcome Measures

Full Information

First Posted
December 14, 2014
Last Updated
May 26, 2015
Sponsor
Chung Shan Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT02456363
Brief Title
Anti-Tumor Necrosis Factor Therapy In Patients With Ankylosing Spondylitis
Official Title
Anti-Tumor Necrosis Factor Therapy In Patients With Ankylosing Spondylitis-A Registry Project
Study Type
Interventional

2. Study Status

Record Verification Date
May 2015
Overall Recruitment Status
Unknown status
Study Start Date
November 2009 (undefined)
Primary Completion Date
October 2019 (Anticipated)
Study Completion Date
December 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chung Shan Medical University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Assessed using (1) Adalimumab(Humira) and NSAIDs (2) Use only Adalimumab(Humira) treatment of ankylosing spondylitis patient safety and efficacy.
Detailed Description
In this study, single center, treatment, open, randomized, controlled clinical trial to assess Adalimumab(Humira) style with NSAIDs for the treatment of patients with ankylosing spondylitis, a total of 300 are expected to be included in the consent form signed by the subject, will be randomly assigned to treatment groups with a control group of 150 people. Subjects to be returned in the first week outpatient follow 0,8,20,44,68,92 accept routine physical examination (weight, blood pressure, etc.), AS Scale (BASDAI, BASFI, BAS-G), fingertip ground tests, lumbar range of motion, chest expansion test, lateral bending test, the occipital bone measurements, physician global assessment (Physician global assessment), patient pain scores (VAS), AS quality of Life scale (ASQOL), SF-36 quality of life scale, Complete joint assessment, ASAS20 response criteria, assessment of laboratory analysis inflammation index (HS-CRP, IgA, ESR), safety index checks (CBC, SGPT, Serum creatinine, HBV-DNA if HbsAg (+), HCV -RNA if HCVAB. Subjects need to return OPD week 0, accept Anti-HBs, Anti-HBc, HBsAg, Anti-HCV. Subjects required to return to the first outpatient follow 0,20,92 weeks, pulmonary function tests. Therefore, the subjects in the 92 weeks of the trial, a total need for blood six times, each time for blood about 10 cc. And to assess side effects and adverse events (Adverse Event, AE), serious adverse events (Serious Adverse Event, SAE)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ankylosing Spondylitis
Keywords
Adalimumab, NSAIDs, safety, efficacy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
NSAIDs(+) and sulfasalazine(+)
Arm Type
Experimental
Arm Description
use TNF alpha: Adalimumab (Humira)、Etanercept (Enbrel) or Golimumab (Simponi) combine with use of NSAIDs and no sulfasalazine
Arm Title
NSAIDs(+) and sulfasalazine(-)
Arm Type
Experimental
Arm Description
use TNF alpha: Adalimumab (Humira)、Etanercept (Enbrel) or Golimumab (Simponi) combine with use of NSAIDs and no sulfasalazine
Arm Title
NSAIDs(-) and sulfasalazine(+)
Arm Type
Experimental
Arm Description
use TNF alpha: Adalimumab (Humira)、Etanercept (Enbrel) or Golimumab (Simponi) combine with use of sulfasalazine and no NSAIDs
Arm Title
NSAIDs(-) and sulfasalazine(-)
Arm Type
Experimental
Arm Description
use TNF alpha: Adalimumab (Humira)、Etanercept (Enbrel) or Golimumab (Simponi) neither NSAIDs nor sulfasalazine
Intervention Type
Biological
Intervention Name(s)
TNF alpha
Other Intervention Name(s)
Drug: Adalimumab (Humira), Drug: Etanercept (Enbrel), Drug: Golimumab (Simponi)
Intervention Description
Depending on patient need to use different TNF alpha
Intervention Type
Drug
Intervention Name(s)
NSAIDs and sulfasalazine
Other Intervention Name(s)
Drug: Arcoxia, Drug: Celebrex, Drug: Tonec, Drug: Mobic, Drug: sulfasalazine
Intervention Description
randomized case, combine with use of NSAIDs(-/+) and sulfasalazine(-/+)
Primary Outcome Measure Information:
Title
mSASSS (Modified Stoke Ankylosing Spondylitis Spinal Score)
Description
weeks 92 of the spinal injury
Time Frame
weeks 92

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥18 years old HLA B27 positive X ray examination Clinical symptoms and physical examination, the following three conditions are subject to at least two: i.lower back pain and morning stiffness symptoms persist more than 3 months ii. lumbar activity is restricted iii. chest expansion is restricted Active disease for four weeks or more (continue two examination BASDAI>6, ESR> 28 mm/1 hr and CRP>1 mg/dl) Exclusion Criteria: pregnant or breast-feeding women patients with active infections highly infectious patients Cancer or precancerous condition of the patient multiple sclerosis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wei C- C, M.D.
Organizational Affiliation
Chung Shan Medical University
Official's Role
Study Director
Facility Information:
Facility Name
Chung Shan Medical University Hospital
City
Taichung
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Cheng-Chung Wei, M.D., Ph.D.
Phone
24739595
Ext
34718
Email
wei3228@gmail.com

12. IPD Sharing Statement

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Anti-Tumor Necrosis Factor Therapy In Patients With Ankylosing Spondylitis

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