Comparison · NCT02080403-sae
Treatment vs Control: serious adverse events
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
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ConductScience Library. Treatment vs Control: serious adverse events. Trial comparisons, record NCT02080403-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02080403-sae
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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 | 0.0274 | 0.0107 | 0.0683 | wilson | |
| Risk in group 2 | 0.0208 | 0.00711 | 0.0595 | wilson | |
| Risk difference, group 1 minus group 2 | 0.00656 | -0.0355 | 0.0497 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.32 | 0.3 | 5.77 | log | |
| Odds ratio, group 1 over group 2 | 1.32 | 0.291 | 6.02 | log | |
| Number needed to harm, for one more participant with a serious adverse event on Treatment than on Control | 152 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: control.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Treatment | Treatment, 2.5 mg Chlorhexidine Gluconate chip (PerioChip®) inserted every two weeks starting at Baseline for the first 3 months, plus mechanical Subgingival Debridement at Baseline and 3 months.~2.5 mg Chlorhexidine gluconate chip: Subgingival debridement will be carried out for each one of the target implant. Upon completion of the debridement a PerioChip® will be inserted in each one of the target implant. | 4 | 146 | EG000 |
| Group 2 | Control | Mechanical Subgingival Debridement at Baseline and 3 months. | 3 | 144 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- Screening through Week 24
Source ClinicalTrials.gov
Trial
- Title
- The Efficacy and Safety of Chlorhexidine Gluconate Chip (PerioChip®) in Therapy of Peri-implantitis
- NCT number
- NCT02080403
- Phases
- PHASE3
- Conditions
- Peri-Implantitis
- Interventions
- 2.5 mg Chlorhexidine gluconate chip
- Lead sponsor
- Dexcel Pharma Technologies Ltd.
- Results first posted
- 2021-06-23
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT02080403?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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