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Completed

NCT Number: NCT00175032

A Comparison of Safety and Treatment in Subjects With Osteoarthritis Taking Low Dose Aspirin

The purpose of this study is to compare the gastroduodenal ulceration rate, gastrointestinal complication rate and non-steroidal anti-inflammatory drug-associated dyspepsia between lansoprazole, naproxen and celecoxib, taken once daily (QD) or twice daily (BID), in participants with osteoarthritis taking low dose aspirin.

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Key information

About this study

This study was designed to compare the effectiveness of reducing the incidence of gastroduodenal ulcers between lansoprazole 30mg QD + naproxen 500mg BID vs celecoxib 200mg QD in subjects with osteoarthritis taking low dose aspirin. Approximately 100 sites across the U.S. will enroll subjects with normal endoscopic findings and negative H.pylori. The duration of the study will be a maximum of 14 weeks including a screening period of up to 2 weeks and a 12 week treatment period. Gelusil will be provided for dyspepsia symptom rescue.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Must require the chronic use of a non-steroidal anti-inflammatory drug for the treatment of osteoarthritis.
  • Must be taking daily aspirin for cardiovascular prophylaxis.
  • Clinical Laboratory values within normal limits for this population

Exclusion criteria

  • History of gastric, duodenal or esophageal surgery except simple oversew of an ulcer.
  • Evidence of uncontrolled, clinically significant disease.
  • History of cancer within the past 5 years.
  • Presence of gastroduodenal ulcers, esophageal ulcer or >= 10 gastroduodenal erosions during the screening endoscopy. Known history of gastroduodenal ulcer or bleeding within the past year. Esophageal stricture requiring dilatation.
  • Presence of Barrett's esophagus with dysplastic changes.
  • Systemic disease affecting the esophagus or a history of caustic or physiochemical trauma or irradiation to the esophagus.
  • Sero-tests positive for H. pylori.
  • Evidence of Zollinger-Ellison syndrome, esophageal varices, cholecystitis, or pancreaticobiliary tract disease.
  • Requires treatment with an excluded medication such as proton pump inhibitors, histamine H2 receptor antagonists, antacids, corticosteroids, lithium, fluconazole, misoprostol, probenecid, methotrexate, anticoagulants, St. John's wart, dong quai, feverfew, garlic, ginger, horse chestnut, red clover or white willow supplements or bisphosphonates.

Treatment and study plan

Lansoprazole and naproxen and aspirin

Drug

Lansoprazole 30 mg, capsules, orally once daily; Naproxen 500 mg, capsules, orally, twice daily; and aspirin 81 mg or 325 mg, tablets, orally, once daily for up to 12 weeks.

Celecoxib and aspirin

Drug

Celecoxib 200 mg, capsules, orally once daily and aspirin 81 mg or 325 mg, tablets, orally, once daily for up to 12 weeks.

Primary outcomes

  1. Gastroduodenal ulcers at final visit

    Time frame: Week 12

Secondary outcomes

  1. Proportion of subjects with GI complications (GI bleeding, perforation and gastric outlet obstruction)

    Time frame: Week 12

  2. Severity of each dyspepsia symptom (abdominal pain, nausea, vomiting, heartburn, fullness, and belching) and combined dyspepsia scores.

    Time frame: Weeks 4,8, and 12

  3. Proportion of subjects with dyspepsia at weeks 4, 8, and 12 that did not have dyspepsia at baseline.

    Time frame: Weeks 4,8, and 12

  4. Proportion of subjects without dyspepsia at weeks 4, 8, and 12 who had dyspepsia at baseline.

    Time frame: Weeks 4, 8, and 12

  5. Scores of each SODA scale (pain intensity, non-pain symptoms, and satisfaction) for subjects with dyspepsia.

    Time frame: Weeks 4, 8, and 12

  6. The change from baseline SODA scale for subjects with dyspepsia at baseline.

    Time frame: Weeks 4, 8, and 12

Sponsors and collaborators

Lead sponsor

Takeda

Industry

Registry information

Official study title

A Randomized, Double-Blind, Phase 3 Study to Compare the Efficacy and Safety of Lansoprazole 30 mg QD and Naproxen 500 mg BID Versus Celecoxib 200 mg QD in Risk Reduction of Non Steroidal Anti-Inflammatory-Associated Ulcers in Osteoarthritis Subjects Taking Low Dose Aspirin

Important dates

Study start
2003
Primary completion
2004
Study completion
2004
First posted
Sep 15, 2005
Registry last updated
Jul 22, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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