Comparison · NCT00527787-a1f5bbb0
PN400 (VIMOVO) vs Naproxen: Heartburn Symptom Resolution, ie no Heartburn Symptoms During the Last 7 Days Prior to the Visit
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. PN400 (VIMOVO) vs Naproxen: Heartburn Symptom Resolution, ie no Heartburn Symptoms During the Last 7 Days Prior to the Visit. Trial comparisons, record NCT00527787-a1f5bbb0. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00527787-a1f5bbb0
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.642 | 0.577 | 0.703 | wilson | |
| Risk in group 2 | 0.301 | 0.244 | 0.365 | wilson | |
| Risk difference, group 1 minus group 2 | 0.341 | 0.249 | 0.425 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 2.13 | 1.7 | 2.68 | log | |
| Odds ratio, group 1 over group 2 | 4.17 | 2.79 | 6.23 | log | |
| Number needed to treat, for one more participant with the outcome on PN400 (VIMOVO) than on Naproxen | 2.93 | 2.35 | 4.01 | from the risk difference interval |
Source ClinicalTrials.gov
Groups2
Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | PN400 (VIMOVO) | Naproxen 500 mg/Immediate-Release Esomeprazole 20 mg | 140 | 218 | OG000 |
| Group 2 | Naproxen | Naproxen 500 mg | 65 | 216 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Heartburn Symptom Resolution, ie no Heartburn Symptoms During the Last 7 Days Prior to the Visit
- Description
Subjects were asked whether heartburn symptoms within the 7 days prior to the visit were:~* none: no symptoms~* mild: awareness of symptom, but easily tolerated~* moderate: discomforting symptom sufficient to cause interference with normal activities (including sleep)~* severe: incapacitating symptom, with inability to perform normal activities (including sleep) Heartburn was defined as a burning feeling rising from the stomach or lower part of the chest towards the neck.
- Time frame
- 6 months
- Population
- Intent to Treat (ITT) Population
Source ClinicalTrials.gov
Trial
- Title
- Evaluating PN 400 (VIMOVO) in Reducing Gastric Ulcers Compared to Non-steroidal Antiinflammatory Drug (NSAID) Naproxen
- NCT number
- NCT00527787
- Phases
- PHASE3
- Conditions
- Gastric Ulcer
- Interventions
- PN400 (VIMOVO), Naproxen
- Lead sponsor
- POZEN
- Results first posted
- 2010-12-28
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00527787?tab=results
Source ClinicalTrials.gov
Source
- Release
- trial-comparisons-2026-03-23-0.1.0
- Release manifest SHA-256
- f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
- AACT copy
- 2026-03-23
- Tables read
- outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet
Source ClinicalTrials.gov
Sources 2
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.
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