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Celecoxib Versus Naproxen for Prevention of Recurrent Ulcer Bleeding in Arthritis Patients

Primary Purpose

Arthritis, Cardiovascular Diseases, Cerebrovascular Disorders

Status
Completed
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Celecoxib(drug)
Naproxen(drug)
Sponsored by
Chinese University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Arthritis

Eligibility Criteria

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

Inclusion Criteria: age >18, a history of endoscopically proven gastroduodenal ulcer bleeding, H. pylori negative a history of cardiothrombotic disease requiring ASA, and anticipated regular use of NSAIDs for the duration of trial Exclusion Criteria: concomitant use of anticoagulants; a history of gastric or duodenal surgery other than a patch repair; the presence of erosive esophagitis, gastric outlet obstruction, renal failure (defined by a serum creatinine level of more than 200 umol/L), pregnancy, terminal illness, or cancer

Sites / Locations

  • Endoscopy Center, Prince of Wales Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

NSAID #1

NSAID #2

Arm Description

Celecoxib and Naproxen Placebo

Naproxen and Celecoxib Placebo

Outcomes

Primary Outcome Measures

Recurrent ulcer bleeding within 18 months according to pre-specified criteria

Secondary Outcome Measures

patients' global assessment of arthritis
major CV events according to the Antithrombotic Trialists' criteria
non-fatal myocardial infarction
non-fatal stroke
death from a vascular cause

Full Information

First Posted
September 7, 2005
Last Updated
December 30, 2016
Sponsor
Chinese University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT00153660
Brief Title
Celecoxib Versus Naproxen for Prevention of Recurrent Ulcer Bleeding in Arthritis Patients
Official Title
A Double-blind Randomized Comparison of Celecoxib Plus Esomeprazole Versus Naproxen Plus Esomeprazole for Prevention of Recurrent Ulcer Bleeding in Patients With Arthritis and Cardiothrombotic Diseases (NSAID#8 Study)
Study Type
Interventional

2. Study Status

Record Verification Date
December 2016
Overall Recruitment Status
Completed
Study Start Date
June 2005 (undefined)
Primary Completion Date
November 2014 (Actual)
Study Completion Date
December 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of this study is to compare celecoxib plus a PPI (esomeprazole) versus naproxen plus a PPI (esomeprazole) in preventing recurrent ulcer bleeding in arthritis patients with a history of ulcer bleeding who require concomitant ASA. We hypothesized that among patients with a history of ulcer bleeding who require concomitant ASA, celecoxib plus esomprazole would be superior to naproxen plus esomeprazole for the prevention of recurrent ulcer bleeding.
Detailed Description
Nonsteroidal anti-inflammatory drugs (NSAIDs) are the most commonly consumed drugs worldwide for the relief of pain and arthritis. However, the use of NSAIDs increases the risk of ulcer bleeding by 4-fold. Current evidence indicates that combination of conventional NSAIDs and a proton pump inhibitor (PPI) reduces the risk of ulcer complications. The alternative strategy is to replace conventional, non-selective NSAIDs with NSAIDs selective for cyclooxygenase-2 (COX-2 inhibitors). Recently, there are concerns about the cardiovascular safety of COX-2 inhibitors and conventional NSAIDs. Because of such concern, patients requiring anti-inflammatory analgesics who have cardiovascular risk factors (e.g. smoking, hypertension, hyperlipidemia, diabetes) should receive prophylactic low-dose aspirin. However, concomitant low-dose aspirin negates the gastric sparing effect of COX-2 inhibitors and augments the gastric toxicity of nonselective NSAIDs. Thus, gastroprotective agents such as PPIs should be co-prescribed to patients with high ulcer risk who are taking aspirin plus a COX-2 inhibitor or a nonselective NSAID.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Arthritis, Cardiovascular Diseases, Cerebrovascular Disorders

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
514 (Actual)

8. Arms, Groups, and Interventions

Arm Title
NSAID #1
Arm Type
Active Comparator
Arm Description
Celecoxib and Naproxen Placebo
Arm Title
NSAID #2
Arm Type
Active Comparator
Arm Description
Naproxen and Celecoxib Placebo
Intervention Type
Drug
Intervention Name(s)
Celecoxib(drug)
Other Intervention Name(s)
Celebrex
Intervention Description
Celecoxib 100 mg bd
Intervention Type
Drug
Intervention Name(s)
Naproxen(drug)
Other Intervention Name(s)
Naprosyn
Intervention Description
Naproxen 500 mg bd
Primary Outcome Measure Information:
Title
Recurrent ulcer bleeding within 18 months according to pre-specified criteria
Time Frame
18 months
Secondary Outcome Measure Information:
Title
patients' global assessment of arthritis
Time Frame
18 months
Title
major CV events according to the Antithrombotic Trialists' criteria
Time Frame
18 months
Title
non-fatal myocardial infarction
Time Frame
18 months
Title
non-fatal stroke
Time Frame
18 months
Title
death from a vascular cause
Time Frame
18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age >18, a history of endoscopically proven gastroduodenal ulcer bleeding, H. pylori negative a history of cardiothrombotic disease requiring ASA, and anticipated regular use of NSAIDs for the duration of trial Exclusion Criteria: concomitant use of anticoagulants; a history of gastric or duodenal surgery other than a patch repair; the presence of erosive esophagitis, gastric outlet obstruction, renal failure (defined by a serum creatinine level of more than 200 umol/L), pregnancy, terminal illness, or cancer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francis K Chan, MD
Organizational Affiliation
Chinese University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Endoscopy Center, Prince of Wales Hospital
City
Shatin
State/Province
Hong Kong
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
28410791
Citation
Chan FKL, Ching JYL, Tse YK, Lam K, Wong GLH, Ng SC, Lee V, Au KWL, Cheong PK, Suen BY, Chan H, Kee KM, Lo A, Wong VWS, Wu JCY, Kyaw MH. Gastrointestinal safety of celecoxib versus naproxen in patients with cardiothrombotic diseases and arthritis after upper gastrointestinal bleeding (CONCERN): an industry-independent, double-blind, double-dummy, randomised trial. Lancet. 2017 Jun 17;389(10087):2375-2382. doi: 10.1016/S0140-6736(17)30981-9. Epub 2017 Apr 11.
Results Reference
derived

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Celecoxib Versus Naproxen for Prevention of Recurrent Ulcer Bleeding in Arthritis Patients

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