Trial · NCT05660135
Reduction Efficacy of OLOMAX for Blood Pressure and Low-density Lipoprotein Cholesterol in Hypertensive Patients With Dyslipidemia
NCT05660135, Active not recruiting, Daewoong Pharmaceutical Co. LTD.
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Reduction Efficacy of OLOMAX for Blood Pressure and Low-density Lipoprotein Cholesterol in Hypertensive Patients With Dyslipidemia. Trials, record NCT05660135. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05660135
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Reduction Efficacy of OLOMAX for Blood Pressure and Low-density Lipoprotein Cholesterol in Hypertensive Patients With Dyslipidemia
- NCT number
- NCT05660135
- Status
- Active not recruiting
- Enrollment
- 4,000 participants, estimated
- Lead sponsor
- Daewoong Pharmaceutical Co. LTD.
- Conditions
- Hypertension, Dyslipidemias
- Interventions
- Olmesartan Medoxomil/ Amlodipine Besylate/ Rosuvastatin Ca
- First posted
- 2022-12-21
- Last updated
- 2025-08-24
Source ClinicalTrials.gov
Registered outcomes14
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | The rate of change in LDL-C | at 24 weeks | The rate of change in LDL-C at 12 weeks from baseline |
| Primary | The amount of change in LDL-C | at 24 weeks | The amount of change in LDL-C at 24 weeks from baseline |
| Secondary | The rate of change in LDL-C | at 12 weeks | The rate of change in LDL-C at 12 weeks from baseline |
| Secondary | The amount of change in LDL-C | at 12 weeks | The amount of change in LDL-C at 12 weeks from baseline |
| Secondary | The rate of change in SBP(Systolic Blood Pressure) | 12 weeks | The rate of change in SBP(Systolic Blood Pressure) at 12 weeks from baseline |
| Secondary | The rate of change in SBP(Systolic Blood Pressure) | 24 weeks | The rate of change in SBP(Systolic Blood Pressure) at 24 weeks from baseline |
| Secondary | The amount of change in SBP(Systolic Blood Pressure) | 12 weeks | The amount of change in SBP(Systolic Blood Pressure) at 12 weeks from baseline |
| Secondary | The amount of change in SBP(Systolic Blood Pressure) | 24 weeks | The amount of change in SBP(Systolic Blood Pressure) at 24 weeks from baseline |
| Secondary | The rate of change in lipid variable(TC, HDL-C, non-HDL-C, TG) | 12 weeks | The rate of change in lipid variable(TC, HDL-C, non-HDL-C, TG) at 12 weeks from baseline |
| Secondary | The rate of change in lipid variable(TC, HDL-C, non-HDL-C, TG) | 24 weeks | The rate of change in lipid variable(TC, HDL-C, non-HDL-C, TG) at 24 weeks from baseline |
1 to 10 of 14Source ClinicalTrials.gov
See all 14 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
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
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT05660135
GET https://conductscience.org/api/trials/v1/NCT05660135/registered