Full Text View
Tabular View
No Study Results Posted
Related Studies
Celecoxib Versus Naproxen for Prevention of Recurrent Ulcer Bleeding in Arthritis Patients
This study is currently recruiting participants.
Verified by Chinese University of Hong Kong, October 2006
First Received: September 7, 2005   Last Updated: March 14, 2008   History of Changes
Sponsored by: Chinese University of Hong Kong
Information provided by: Chinese University of Hong Kong
ClinicalTrials.gov Identifier: NCT00153660
  Purpose

The purpose of this study is to compare a PPI (esomeprazole) plus a COX-2 inhibitor (celecoxib) with a PPI plus a nonselective NSAID (naproxen) in preventing recurrent ulcer bleeding in arthritis patients who receive concomitant low-dose aspirin.


Condition Intervention
Arthritis
Cardiovascular Diseases
Cerebrovascular Disorders
Drug: Celecoxib(drug)
Drug: Naproxen(drug)

Study Type: Interventional
Study Design: Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Active Control, Parallel Assignment, Safety Study
Official Title: Phase III Study of a Double-Blind Randomized Comparison of Esomeprazole Plus Celecoxib Versus Esomeprazole Plus Naproxen for Prevention of Recurrent Ulcer Bleeding in Arthritis Patients Receiving Concomitant Low-Dose Aspirin (NSAID#8 Study)

Resource links provided by NLM:


Further study details as provided by Chinese University of Hong Kong:

Primary Outcome Measures:
  • Recurrent ulcer bleeding within 78 weeks according to pre-specified criteria [ Time Frame: 78 weeks ]

Secondary Outcome Measures:
  • Cardiovascular events [ Time Frame: 78 weeks ]

Estimated Enrollment: 322
Study Start Date: June 2005
Estimated Primary Completion Date: June 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Active Comparator
Celecoxib
Drug: Celecoxib(drug)
Celecoxib 100 mg bd
2: Active Comparator
Naproxen
Drug: Naproxen(drug)
Naproxen 500 mg bd

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.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Indications for prophylactic low-dose aspirin according to American Heart Association/American Diabetes Association guidelines
  • A negative test for Helicobacter pylori or successful eradication of Helicobacter pylori according to histology
  • Anticipated regular use of NSAIDs for the duration of the 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
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00153660

Contacts
Contact: Francis K Chan, MD 85226323143 fklchan@cuhk.edu.hk
Contact: Jessica Y Ching, MPH 85226323524 jessicaching@cuhk.edu.hk

Locations
China
Endoscopy Center, Prince of Wales Hospital Recruiting
Hong Kong, China
Contact: Franics K Chan, MD     26323143     fklchan@cuhk.edu.hk    
Contact: Jessica Y Ching, MPH     26323524     jessicaching@cuhk.edu.hk    
Sub-Investigator: Vincent W Wong, MD            
Principal Investigator: Francis K Chan, MD            
Sponsors and Collaborators
Chinese University of Hong Kong
Investigators
Principal Investigator: Francis K Chan, MD Chinese University of Hong Kong
  More Information

No publications provided

Responsible Party: Chinese University of Hong Kong ( Francis K CHAN )
Study ID Numbers: 8N Study
Study First Received: September 7, 2005
Last Updated: March 14, 2008
ClinicalTrials.gov Identifier: NCT00153660     History of Changes
Health Authority: Hong Kong: Department of Health

Study placed in the following topic categories:
Anti-Inflammatory Agents
Celecoxib
Naproxen
Ulcer
Joint Diseases
Cyclooxygenase Inhibitors
Vascular Diseases
Omeprazole
Central Nervous System Diseases
Hemorrhage
Brain Diseases
Cerebrovascular Disorders
Recurrence
Musculoskeletal Diseases
Aspirin
Analgesics, Non-Narcotic
Arthritis
Anti-Inflammatory Agents, Non-Steroidal
Peripheral Nervous System Agents
Analgesics
Antirheumatic Agents

Additional relevant MeSH terms:
Anti-Inflammatory Agents
Molecular Mechanisms of Pharmacological Action
Physiological Effects of Drugs
Brain Diseases
Cerebrovascular Disorders
Gout Suppressants
Musculoskeletal Diseases
Sensory System Agents
Arthritis
Therapeutic Uses
Anti-Inflammatory Agents, Non-Steroidal
Cardiovascular Diseases
Analgesics
Celecoxib
Naproxen
Joint Diseases
Nervous System Diseases
Cyclooxygenase Inhibitors
Vascular Diseases
Central Nervous System Diseases
Enzyme Inhibitors
Pharmacologic Actions
Analgesics, Non-Narcotic
Peripheral Nervous System Agents
Antirheumatic Agents
Central Nervous System Agents

ClinicalTrials.gov processed this record on August 30, 2009