Disease · MONDO_0002146
Comparisons in its trials42
Comparisons Trial comparisons calculated in the trials shown here, most participants first. A comparison in one of these trials does not always compare a treatment for the disease, so read the two groups.
1 to 20 of 42
Download this page as JSON| Comparison | Group 1, with the outcome | Group 2, with the outcome | Participants | Trial | Source |
|---|---|---|---|---|---|
| AndroGel 1.62% vs Placebo: Time From Randomization to First Clinical Fracture: Number and Percentage of Participants With an Event | 91 of 2,601 | 64 of 2,603 | 5,204 | NCT03518034 | Trial comparisons |
| AndroGel 1.62% vs Placebo: Tertiary Endpoint: Incidence Rate of Heart Failure | 55 of 2,596 | 50 of 2,602 | 5,198 | NCT03518034 | Trial comparisons |
| AndroGel 1.62% vs Placebo: Tertiary Endpoint: Incidence Rate of All Cause Mortality | 144 of 2,596 | 148 of 2,602 | 5,198 | NCT03518034 | Trial comparisons |
| AndroGel 1.62% vs Placebo: Tertiary Endpoint: Incidence Rate of Prostate Cancer | 12 of 2,596 | 11 of 2,602 | 5,198 | NCT03518034 | Trial comparisons |
| AndroGel 1.62% vs Placebo: Time From Randomization to the First Component Event of Major Adverse Cardiac Event (MACE): Number and Percentage of Participants With an Event | 182 of 2,596 | 190 of 2,602 | 5,198 | NCT03518034 | Trial comparisons |
| AndroGel 1.62% vs Placebo: Tertiary Endpoint: Incidence Rate of Acute Urinary Retention | 20 of 2,596 | 16 of 2,602 | 5,198 | NCT03518034 | Trial comparisons |
| AndroGel 1.62% vs Placebo: Tertiary Endpoint: Incidence Rate of Pharmacologic Treatment for Lower Urinary Tract Symptoms | 101 of 2,596 | 87 of 2,602 | 5,198 | NCT03518034 | Trial comparisons |
| AndroGel 1.62% vs Placebo: Tertiary Endpoint: Incidence Rate of Peripheral Arterial Revascularization | 30 of 2,596 | 33 of 2,602 | 5,198 | NCT03518034 | Trial comparisons |
| AndroGel 1.62% vs Placebo: Tertiary Endpoint: Incidence Rate of Invasive Prostate Surgical Procedures for Benign Prostatic Hyperplasia | 23 of 2,596 | 12 of 2,602 | 5,198 | NCT03518034 | Trial comparisons |
| AndroGel 1.62% vs Placebo: Incidence of High-Grade Prostate Cancer | 5 of 2,596 | 3 of 2,602 | 5,198 | NCT03518034 | Trial comparisons |
| AndroGel 1.62% vs Placebo: Time From Randomization to the First Component Event of CV Safety Endpoint: Number and Percentage of Participants With an Event | 269 of 2,596 | 264 of 2,602 | 5,198 | NCT03518034 | Trial comparisons |
| AndroGel 1.62% vs Placebo: Tertiary Endpoint: Incidence Rate of Prostate Biopsy | 16 of 2,596 | 14 of 2,602 | 5,198 | NCT03518034 | Trial comparisons |
| AndroGel 1.62% vs Placebo: Tertiary Endpoint: Incidence Rate of Venous Thromboembolic Events | 44 of 2,596 | 30 of 2,602 | 5,198 | NCT03518034 | Trial comparisons |
| Testosterone Solution vs Placebo Solution: Number of Participants With Total Serum Testosterone Concentration Within Normal Range at Week 12 | 217 of 297 | 43 of 287 | 584 | NCT01816295 | Trial comparisons |
| TU 750 mg vs TU 1000 mg: serious adverse events | 38 of 272 | 37 of 252 | 524 | NCT00467870 | Trial comparisons |
| Oral Testosterone Undecanoate (TU) vs Topical Testosterone Gel: deaths from any cause | 0 of 161 | 0 of 160 | 321 | NCT01403116 | Trial comparisons |
| Oral Testosterone Undecanoate (TU) vs Topical Testosterone Gel: serious adverse events | 11 of 161 | 6 of 160 | 321 | NCT01403116 | Trial comparisons |
| SOV2012-F1-Treated vs Andro-Gel Treated: deaths from any cause | 1 of 214 | 0 of 100 | 314 | NCT03198728 | Trial comparisons |
| SOV2012-F1-Treated vs Andro-Gel Treated: serious adverse events | 9 of 214 | 1 of 100 | 314 | NCT03198728 | Trial comparisons |
| T-Gel 1.62% vs Placebo: serious adverse events | 5 of 234 | 1 of 40 | 274 | NCT00433199 | Trial comparisons |
diseases-2026-09-18-0.1.0
Sources 6
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- NLM's MeSHNLM's terms
- Open TargetsCC0 1.0
- PubMedNLM's terms
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
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- NLM's MeSHNLM's
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PubMedNLM's terms
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/diseases/v1/MONDO_0002146/comparisons