Comparison · NCT02084134-2fe7cb60
Steroid Treatment Arm vs Non-steroid Treatment: Number of Participants With Adrenal Insufficiency
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. Steroid Treatment Arm vs Non-steroid Treatment: Number of Participants With Adrenal Insufficiency. Trial comparisons, record NCT02084134-2fe7cb60. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02084134-2fe7cb60
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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 | 0.105 | 0.0294 | 0.314 | wilson | |
| Risk in group 2 | 0.0588 | 0.0105 | 0.27 | wilson | |
| Risk difference, group 1 minus group 2 | 0.0464 | -0.178 | 0.261 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.79 | 0.178 | 18 | log | |
| Odds ratio, group 1 over group 2 | 1.88 | 0.155 | 22.8 | log | |
| Number needed to treat, for one more participant with the outcome on Steroid Treatment Arm than on Non-steroid Treatment | 21.5 | 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 | Steroid Treatment Arm | Receives intravenous hydrocortisone 100mg and following surgery intravenous dexamethasone 0.5mg~hydrocortisone: 100mg at the time of surgery~dexamethasone: 0.5mg every 6 hours for a total of four doses | 2 | 19 | OG000 |
| Group 2 | Non-steroid Treatment | Subjects will not receive any steroids at the time of surgery or after surgery unless symptoms of adrenal insufficiency develop (i.e. nausea, vomiting, dizziness, or low blood pressure). | 1 | 17 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- PRIMARY
- Title
- Number of Participants With Adrenal Insufficiency
- Description
- Adrenal insufficiency was defined by a 30 or 60 min cortisol \< 18 during a cosyntropin stimulation test
- Time frame
- 6 weeks following surgery
- Population
Source ClinicalTrials.gov
Trial
- Title
- Peri-Operative Steroid Management in Patients
- NCT number
- NCT02084134
- Phases
- NA
- Conditions
- Pituitary Adenoma, Pituitary Diseases
- Interventions
- hydrocortisone, dexamethasone
- Lead sponsor
- Washington University School of Medicine
- Results first posted
- 2018-03-01
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT02084134?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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