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Trial ยท NCT00696436

An Efficacy and Safety Study of Azilsartan Medoxomil Compared to Valsartan and Olmesartan in Participants With Essential Hypertension.

NCT00696436, Phase 3, Completed, Takeda; results first posted 2011-04-19

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. An Efficacy and Safety Study of Azilsartan Medoxomil Compared to Valsartan and Olmesartan in Participants With Essential Hypertension. Trials, record NCT00696436. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00696436

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Trial

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

Title
An Efficacy and Safety Study of Azilsartan Medoxomil Compared to Valsartan and Olmesartan in Participants With Essential Hypertension.
NCT number
NCT00696436
Status
Completed
Phases
Phase 3
Enrollment
1,291 participants, actual
Lead sponsor
Takeda
Conditions
Hypertension
Interventions
Azilsartan medoxomil, Azilsartan medoxomil, Valsartan, Olmesartan, Placebo
First posted
2008-06-12
Last updated
2011-04-19
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 Pressure.Baseline 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 systolic 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 Monitoring.Baseline 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 Monitoring.Baseline 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.mmHgLEAST_SQUARES_MEAN
SECONDARYChange From Baseline in Mean Trough Clinic Sitting Systolic Blood Pressure.Baseline 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.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.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.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.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.mmHgLEAST_SQUARES_MEAN
SECONDARYChange From Baseline in the 12-hour Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Baseline and Week 6.Full Analysis Set.mmHgLEAST_SQUARES_MEAN
SECONDARYChange From Baseline in the 12-hour Mean Diastolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Baseline and Week 6.Full Analysis Set.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 40 mg QD-13.42Standard Error 0.690mmHg
Change From Baseline in the 24-hour Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Azilsartan Medoxomil 80 mg QD-14.53Standard Error 0.702mmHg
Change From Baseline in the 24-hour Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Valsartan 320 mg QD-10.22Standard Error 0.696mmHg
Change From Baseline in the 24-hour Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Olmesartan 40 mg QD-11.99Standard Error 0.666mmHg
Change From Baseline in the 24-hour Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.Placebo QD-0.25Standard Error 0.917mmHg
Change From Baseline in Mean Trough Clinic Sitting Systolic Blood Pressure.Azilsartan Medoxomil 40 mg QD-16.38Standard Error 0.959mmHg
Change From Baseline in Mean Trough Clinic Sitting Systolic Blood Pressure.Azilsartan Medoxomil 80 mg QD-16.74Standard Error 0.957mmHg
Change From Baseline in Mean Trough Clinic Sitting Systolic Blood Pressure.Valsartan 320 mg QD-11.31Standard Error 0.955mmHg
Change From Baseline in Mean Trough Clinic Sitting Systolic Blood Pressure.Olmesartan 40 mg QD-13.20Standard Error 0.935mmHg
Change From Baseline in Mean Trough Clinic Sitting Systolic Blood Pressure.Placebo QD-1.83Standard Error 1.293mmHg

Participant flow15

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDAzilsartan Medoxomil 40 mg QD280
Overall StudySTARTEDAzilsartan Medoxomil 80 mg QD285
Overall StudySTARTEDValsartan 320 mg QD282
Overall StudySTARTEDOlmesartan 40 mg QD290
Overall StudySTARTEDPlacebo QD154
Overall StudyCOMPLETEDAzilsartan Medoxomil 40 mg QD257
Overall StudyCOMPLETEDAzilsartan Medoxomil 80 mg QD255
Overall StudyCOMPLETEDValsartan 320 mg QD254
Overall StudyCOMPLETEDOlmesartan 40 mg QD268
Overall StudyCOMPLETEDPlacebo QD141

Adverse events85

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherHeadacheNervous system disordersAzilsartan Medoxomil 40 mg QD18280
otherHeadacheNervous system disordersAzilsartan Medoxomil 80 mg QD12284
otherHeadacheNervous system disordersValsartan 320 mg QD21277
otherHeadacheNervous system disordersOlmesartan 40 mg QD23290
otherHeadacheNervous system disordersPlacebo QD14155
seriousEye irritationEye disordersAzilsartan Medoxomil 40 mg QD0280
seriousEye irritationEye disordersAzilsartan Medoxomil 80 mg QD1284
seriousEye irritationEye disordersValsartan 320 mg QD0277
seriousEye irritationEye disordersOlmesartan 40 mg QD0290
seriousEye irritationEye disordersPlacebo QD0155

Adverse event totals15

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityAzilsartan Medoxomil 40 mg QD
Total, all-cause mortalityAzilsartan Medoxomil 80 mg QD
Total, all-cause mortalityValsartan 320 mg QD
Total, all-cause mortalityOlmesartan 40 mg QD
Total, all-cause mortalityPlacebo QD
Total, other adverse eventsAzilsartan Medoxomil 40 mg QD18280
Total, other adverse eventsAzilsartan Medoxomil 80 mg QD12284
Total, other adverse eventsValsartan 320 mg QD21277
Total, other adverse eventsOlmesartan 40 mg QD23290
Total, other adverse eventsPlacebo QD14155

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
21282560RESULT

Source PubMed

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/NCT00696436

GET https://conductscience.org/api/trials/v1/NCT00696436/results?page=2