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Trial ยท NCT00696241

Efficacy and Safety of Azilsartan Medoxomil in Participants With Essential Hypertension

NCT00696241, Phase 3, Completed, Takeda; results first posted 2011-04-19

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Efficacy and Safety of Azilsartan Medoxomil in Participants With Essential Hypertension. Trials, record NCT00696241. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00696241

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Efficacy and Safety of Azilsartan Medoxomil in Participants With Essential Hypertension
NCT number
NCT00696241
Status
Completed
Phases
Phase 3
Enrollment
1,275 participants, actual
Lead sponsor
Takeda
Conditions
Hypertension
Interventions
Azilsartan medoxomil and olmesartan, Azilsartan medoxomil and olmesartan, Azilsartan medoxomil and olmesartan, Olmesartan, Placebo
First posted
2008-06-12
Last updated
2011-07-29
Results first posted
2011-04-19

Source ClinicalTrials.gov

Registered outcomes15

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryChange From Baseline in the 24-hour Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Baseline and Week 6.
The change in 24-hour mean systolic blood pressure measured at week 6 relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. The 24-hour mean is the average of all measurements recorded for 24 hours after dosing.
SecondaryChange From Baseline in Mean Trough Clinic Sitting Systolic Blood PressureBaseline and Week 6.The change in mean trough clinic sitting systolic blood pressure measured at final visit or week 6 relative to baseline.
SecondaryChange From Baseline in the 24-hour Mean Diastolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Baseline and Week 6.
The change in 24-hour mean diastolic blood pressure measured at week 6 relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. The 24-hour mean is the average of all measurements recorded for 24 hours after dosing.
SecondaryChange From Baseline in Mean Trough Clinic Sitting Diastolic Blood PressureBaseline and Week 6.The change in mean trough clinic sitting diastolic blood pressure measured at final visit or week 6 relative to baseline.
SecondaryChange From Baseline in Daytime (6am to 10 pm) Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Baseline and Week 6.
The change in daytime (6am to 10pm) mean systolic blood pressure measured at week 6 relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. Daytime mean is the average of all measurements recorded between the hours of 6 am and 10 pm.
SecondaryChange From Baseline in Daytime (6am to 10 pm) Mean Diastolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Baseline and Week 6.
The change in daytime (6am to 10pm) mean diastolic blood pressure measured at week 6 relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. Daytime mean is the average of all measurements recorded between the hours of 6 am and 10 pm.
SecondaryChange From Baseline in the Nighttime (12 am to 6 am) Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Baseline and Week 6.
The change in nighttime (12am to 6am) mean systolic blood pressure measured at week 6 relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. Nighttime mean is the average of all measurements recorded between the hours of 12 am and 6 am.
SecondaryChange From Baseline in the Nighttime (12 am to 6 am) Mean Diastolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Baseline and Week 6.
The change in nighttime (12am to 6am) mean diastolic blood pressure measured at week 6 relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. Nighttime mean is the average of all measurements recorded between the hours of 12 am and 6 am.
SecondaryChange From Baseline in the 12-hour Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure MonitoringBaseline and Week 6.
The change in the 12-hour mean systolic blood pressure measured at week 6 relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. The 12-hour mean is the average of all measurements recorded in the first 12 hours after dosing.
SecondaryChange From Baseline in the 12-hour Mean Diastolic Blood Pressure Measured by Ambulatory Blood Pressure MonitoringBaseline and Week 6.
The change in the 12-hour mean diastolic blood pressure measured at week 6 relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. The 12-hour mean is the average of all measurements recorded in the first 12 hours after dosing.

Outcomes15

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange From Baseline in the 24-hour Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Baseline and Week 6.Full analysis set with last observation carried forward.mmHgLEAST_SQUARES_MEAN
SECONDARYChange From Baseline in Mean Trough Clinic Sitting Systolic Blood PressureBaseline and Week 6.Full analysis set with last observation carried forward.mmHgLEAST_SQUARES_MEAN
SECONDARYChange From Baseline in the 24-hour Mean Diastolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Baseline and Week 6.Full analysis set with last observation carried forward.mmHgLEAST_SQUARES_MEAN
SECONDARYChange From Baseline in Mean Trough Clinic Sitting Diastolic Blood PressureBaseline and Week 6.Full analysis set with last observation carried forward.mmHgLEAST_SQUARES_MEAN
SECONDARYChange From Baseline in Daytime (6am to 10 pm) Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Baseline and Week 6.Full analysis set with last observation carried forward.mmHgLEAST_SQUARES_MEAN
SECONDARYChange From Baseline in Daytime (6am to 10 pm) Mean Diastolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Baseline and Week 6.Full analysis set with last observation carried forward.mmHgLEAST_SQUARES_MEAN
SECONDARYChange From Baseline in the Nighttime (12 am to 6 am) Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Baseline and Week 6.Full analysis set with last observation carried forward.mmHgLEAST_SQUARES_MEAN
SECONDARYChange From Baseline in the Nighttime (12 am to 6 am) Mean Diastolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Baseline and Week 6.Full analysis set with last observation carried forward.mmHgLEAST_SQUARES_MEAN
SECONDARYChange From Baseline in the 12-hour Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure MonitoringBaseline and Week 6.Full analysis set with last observation carried forward.mmHgLEAST_SQUARES_MEAN
SECONDARYChange From Baseline in the 12-hour Mean Diastolic Blood Pressure Measured by Ambulatory Blood Pressure MonitoringBaseline and Week 6.Full analysis set with last observation carried forward.mmHgLEAST_SQUARES_MEAN

Results by group75

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Change From Baseline in the 24-hour Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Azilsartan Medoxomil 20 mg QD-12.15Standard Error 0.709mmHg
Change From Baseline in the 24-hour Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Azilsartan Medoxomil 40 mg QD-13.48Standard Error 0.704mmHg
Change From Baseline in the 24-hour Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Azilsartan Medoxomil 80 mg QD-14.62Standard Error 0.706mmHg
Change From Baseline in the 24-hour Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Olmesartan 40 mg QD-12.56Standard Error 0.696mmHg
Change From Baseline in the 24-hour Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Placebo QD-1.40Standard Error 1.004mmHg
Change From Baseline in Mean Trough Clinic Sitting Systolic Blood PressureAzilsartan Medoxomil 20 mg QD-14.28Standard Error 0.956mmHg
Change From Baseline in Mean Trough Clinic Sitting Systolic Blood PressureAzilsartan Medoxomil 40 mg QD-14.47Standard Error 0.952mmHg
Change From Baseline in Mean Trough Clinic Sitting Systolic Blood PressureAzilsartan Medoxomil 80 mg QD-17.58Standard Error 0.947mmHg
Change From Baseline in Mean Trough Clinic Sitting Systolic Blood PressureOlmesartan 40 mg QD-14.87Standard Error 0.945mmHg
Change From Baseline in Mean Trough Clinic Sitting Systolic Blood PressurePlacebo QD-2.06Standard Error 1.337mmHg

Participant flow15

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDAzilsartan Medoxomil 20 mg QD283
Overall StudySTARTEDAzilsartan Medoxomil 40 mg QD283
Overall StudySTARTEDAzilsartan Medoxomil 80 mg QD285
Overall StudySTARTEDOlmesartan 40 mg QD282
Overall StudySTARTEDPlacebo QD142
Overall StudyCOMPLETEDAzilsartan Medoxomil 20 mg QD259
Overall StudyCOMPLETEDAzilsartan Medoxomil 40 mg QD261
Overall StudyCOMPLETEDAzilsartan Medoxomil 80 mg QD261
Overall StudyCOMPLETEDOlmesartan 40 mg QD268
Overall StudyCOMPLETEDPlacebo QD130

Adverse events95

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherHeadacheNervous system disordersAzilsartan Medoxomil 20 mg QD13283
otherHeadacheNervous system disordersAzilsartan Medoxomil 40 mg QD9281
otherHeadacheNervous system disordersAzilsartan Medoxomil 80 mg QD16284
otherHeadacheNervous system disordersOlmesartan 40 mg QD9282
otherHeadacheNervous system disordersPlacebo QD10142
otherDyslipidemiaMetabolism and nutrition disordersAzilsartan Medoxomil 20 mg QD10283
otherDyslipidemiaMetabolism and nutrition disordersAzilsartan Medoxomil 40 mg QD11281
otherDyslipidemiaMetabolism and nutrition disordersAzilsartan Medoxomil 80 mg QD16284
otherDyslipidemiaMetabolism and nutrition disordersOlmesartan 40 mg QD10282
otherDyslipidemiaMetabolism and nutrition disordersPlacebo QD3142

Adverse event totals15

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityAzilsartan Medoxomil 20 mg QD
Total, all-cause mortalityAzilsartan Medoxomil 40 mg QD
Total, all-cause mortalityAzilsartan Medoxomil 80 mg QD
Total, all-cause mortalityOlmesartan 40 mg QD
Total, all-cause mortalityPlacebo QD
Total, other adverse eventsAzilsartan Medoxomil 20 mg QD23283
Total, other adverse eventsAzilsartan Medoxomil 40 mg QD19281
Total, other adverse eventsAzilsartan Medoxomil 80 mg QD32284
Total, other adverse eventsOlmesartan 40 mg QD18282
Total, other adverse eventsPlacebo QD13142

Papers2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
21272195RESULTPubMed
21282560RESULTPubMed

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT00696241

GET https://conductscience.org/api/trials/v1/NCT00696241/results?page=2