Disease · MONDO_0005044
Comparisons in its trials305
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 305
Download this page as JSON| Comparison | Group 1, with the outcome | Group 2, with the outcome | Participants | Trial | Source |
|---|---|---|---|---|---|
| Caduet vs Usual Care: serious adverse events | 51 of 779 | 22 of 682 | 1,461 | NCT00407537 | Trial comparisons |
| Telmisartan 40mg and Amlodipine 10mg vs Telmisartan 80mg and Amlodipine 10mg: serious adverse events | 4 of 838 | 13 of 611 | 1,449 | NCT00624052 | Trial comparisons |
| Telmisartan 40mg and Amlodipine 5mg vs Telmisartan 80mg and Amlodipine 5mg: serious adverse events | 22 of 976 | 6 of 397 | 1,373 | NCT00614380 | Trial comparisons |
| Without Concomitant Drugs vs With Concomitant Drugs: Risk Factors for Incidence Rate of Treatment Related Adverse Events(TRAEs) of Amlodipine/Atorvastatin Combination Tablets -Concomitant Drugs. | 3 of 360 | 15 of 885 | 1,245 | NCT01107743 | Trial comparisons |
| Male vs Female: Risk Factors for Incidence Rate of Treatment Related Adverse Events(TRAEs) of Amlodipine/Atorvastatin Combination Tablets -Gender. | 7 of 458 | 11 of 787 | 1,245 | NCT01107743 | Trial comparisons |
| Without Hypertension vs With Hypertension: Risk Factors for Incidence Rate of Treatment Related Adverse Events(TRAEs) of Amlodipine/Atorvastatin Combination Tablets -Hypertension. | 0 of 8 | 18 of 1,237 | 1,245 | NCT01107743 | Trial comparisons |
Without Hypercholesterolemia vs With Hypercholesterolemia: Risk Factors for Incidence Rate of Treatment Related Adverse Events(TRAEs) of Amlodipine/Atorvastatin Combination Tablets -Hypercholesterolemia. | 0 of 18 | 18 of 1,227 | 1,245 | NCT01107743 | Trial comparisons |
| Without Complications vs With Complications: Risk Factors for Incidence Rate of Treatment Related Adverse Events(TRAEs) of Amlodipine/Atorvastatin Combination Tablets -Complications. | 5 of 568 | 13 of 677 | 1,245 | NCT01107743 | Trial comparisons |
| <65 Years vs >=65 Years: Risk Factors for Incidence Rate of Treatment Related Adverse Events(TRAEs) of Amlodipine/Atorvastatin Combination Tablets -Age. | 5 of 377 | 13 of 868 | 1,245 | NCT01107743 | Trial comparisons |
| Without Angina Pectoris vs With Angina Pectoris: Risk Factors for Incidence Rate of Treatment Related Adverse Events(TRAEs) of Amlodipine/Atorvastatin Combination Tablets -Angina Pectoris. | 18 of 1,062 | 0 of 183 | 1,245 | NCT01107743 | Trial comparisons |
Without Familial Hypercholesterolemia vs With Familial Hypercholesterolemia: Risk Factors for Incidence Rate of Treatment Related Adverse Events(TRAEs) of Amlodipine/Atorvastatin Combination Tablets -Familial Hypercholesterolemia. | 18 of 1,231 | 0 of 14 | 1,245 | NCT01107743 | Trial comparisons |
| Without Hepatic Dysfunction vs With Hepatic Dysfunction: Risk Factors for Incidence Rate of Treatment Related Adverse Events(TRAEs) of Amlodipine/Atorvastatin Combination Tablets -Hepatic Dysfunction. | 14 of 1,087 | 2 of 145 | 1,232 | NCT01107743 | Trial comparisons |
| Without Renal Dysfunction vs With Renal Dysfunction: Risk Factors for Incidence Rate of Treatment Related Adverse Events(TRAEs) of Amlodipine/Atorvastatin Combination Tablets -Renal Dysfunction. | 14 of 1,123 | 2 of 108 | 1,231 | NCT01107743 | Trial comparisons |
| <65 Years vs >=65 Years: Risk Factors for the Proportion of Responders for Hypertension -Age. | 347 of 365 | 804 of 837 | 1,202 | NCT01107743 | Trial comparisons |
| Male vs Female: Risk Factors for the Proportion of Responders for Hypertension -Gender. | 415 of 438 | 736 of 764 | 1,202 | NCT01107743 | Trial comparisons |
| Without Concomitant Drugs vs With Concomitant Drugs: Risk Factors for the Proportion of Responders for Hypertension -Concomitant Drugs. | 339 of 355 | 812 of 847 | 1,202 | NCT01107743 | Trial comparisons |
| Without Complications vs With Complications: Risk Factors for the Proportion of Responders for Hypertension -Complications. | 527 of 555 | 624 of 647 | 1,202 | NCT01107743 | Trial comparisons |
| Without Hepatic Dysfunction vs With Hepatic Dysfunction: Risk Factors for the Proportion of Responders for Hypertension -Hepatic Dysfunction. | 1,008 of 1,053 | 131 of 137 | 1,190 | NCT01107743 | Trial comparisons |
| Without Renal Dysfunction vs With Renal Dysfunction: Risk Factors for the Proportion of Responders for Hypertension -Renal Dysfunction. | 1,036 of 1,085 | 102 of 104 | 1,189 | NCT01107743 | Trial comparisons |
| Without Complications vs With Complications: Risk Factors for the Proportion of Responders for Hypercholesterolemia or Familial Hypercholesterolemia -Complications. | 482 of 492 | 552 of 565 | 1,057 | NCT01107743 | 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_0005044/comparisons