Comparison · NCT02722278-7bee4a5d
Oral TU Cosyntropin Substudy Subjects vs Axiron Cosyntropin Substudy Subjects: Number of Participants With Post-stimulation Cortisol Level of >18 ug/dL at Visit 8
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. Oral TU Cosyntropin Substudy Subjects vs Axiron Cosyntropin Substudy Subjects: Number of Participants With Post-stimulation Cortisol Level of >18 ug/dL at Visit 8. Trial comparisons, record NCT02722278-7bee4a5d. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02722278-7bee4a5d
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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 | 0.792 | 0.595 | 0.908 | wilson | |
| Risk in group 2 | 1 | 0.676 | 1 | wilson | |
| Risk difference, group 1 minus group 2 | -0.208 | -0.405 | 0.136 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.792 | 0.645 | 0.972 | log | |
| Odds ratio, group 1 over group 2 | log | a cell of the two-by-two table is zero | |||
| Number needed to treat, for one fewer participant with the outcome on Oral TU Cosyntropin Substudy Subjects than on Axiron Cosyntropin Substudy Subjects | 4.8 | from the risk difference interval | the interval includes no difference |
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 | Oral TU Cosyntropin Substudy Subjects | Subjects receiving Oral TU participating in cosyntropin substudy | 19 | 24 | OG000 |
| Group 2 | Axiron Cosyntropin Substudy Subjects | 8 | 8 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- OTHER_PRE_SPECIFIED
- Title
- Number of Participants With Post-stimulation Cortisol Level of >18 ug/dL at Visit 8
- Description
Compare the Oral TU-treated subjects and the Topical Axiron®-treated subjects with respect to number of subjects in the cosyntropin stimulation test substudy with a normal maximum post-stimulation (cosyntropin stimulation) cortisol level at Visit 8.
- Time frame
- Approximately 4.5 months
- Population
Source ClinicalTrials.gov
Trial
- Title
- A Study of Oral Testosterone Undecanoate (TU) in Hypogonadal Men
- NCT number
- NCT02722278
- Phases
- PHASE3
- Conditions
- Hypogonadism
- Interventions
- Oral Testosterone Undecanoate, Axiron Testosterone Topical Solution
- Lead sponsor
- Clarus Therapeutics, Inc.
- Results first posted
- 2018-02-23
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT02722278?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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