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Trial · NCT05377203

Registered outcomes22

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

ListOutcomeTime frameDescription
PrimaryMean systolic blood pressure of 24-hourFour weeksThe reduction of mean systolic blood pressure of 24-hour in Ambulatory Blood Pressure Monitoring (ABPM) after 4 weeks of medication (from baseline).
SecondaryMean systolic blood pressure of daytime and nightFour weeksThe reduction of mean systolic blood pressure of daytime and night in ABPM after 4 weeks of medication (from baseline).
SecondaryMean diastolic blood pressure of 24-hour, daytime and nightFour weeksThe reduction of mean diastolic blood pressure of 24-hour, daytime and night in ABPM after 4 weeks of medication (from baseline).
SecondaryMorning blood pressure surgeFour weeksThe change of morning blood pressure surge in ABPM after 4 weeks of medication (from baseline).
SecondaryOffice blood pressureFour weeksThe reduction of office blood pressure after 4 weeks of medication (from baseline).
SecondaryHome blood pressureFour weeksThe reduction of home blood pressure after 4 weeks of medication (from baseline).
SecondaryHeart rateFour weeksThe change in heart rate after 4 weeks of medication (from baseline).
SecondaryControlled rate of blood pressureFour weeksControlled rate of blood pressure after 4 weeks of medication (from baseline).
OtherPercentage of participants with severe adverse events (SAE)Four weeksPercentage of participants with any SAE according to Good Clinical Practice definition.
OtherPercentage of participants with side effectsFour weeksPercentage of participants with occurrence of any potentially relevant side effect (pre-specified as in study protocol).
OtherRate of relevant side effectsFour weeksRate of relevant side effects (pre-specified as in study protocol) at the participant level.
OtherMean change in serum potassiumFour weeksMean change (from baseline) in serum potassium after 4 weeks of medication.
OtherMean change in serum sodiumFour weeksMean change (from baseline) in serum sodium after 4 weeks of medication.
OtherMean change in blood urea nitrogenFour weeksMean change (from baseline) in blood urea nitrogen after 4 weeks of medication.
OtherMean change in serum creatinineFour weeksMean change (from baseline) in serum creatinine after 4 weeks of medication.
OtherMean change in serum uric acidFour weeksMean change (from baseline) in serum uric acid after 4 weeks of medication.
OtherMean change in serum glutamic-oxalacetic transaminaseFour weeksMean change (from baseline) in serum glutamic-oxalacetic transaminase after 4 weeks of medication.
OtherMean change in serum glutamic-pyruvic transaminaseFour weeksMean change (from baseline) in serum glutamic-pyruvic transaminase after 4 weeks of medication.
OtherMean change in serum bilirubinFour weeksMean change (from baseline) in serum bilirubin (total and direct bilirubin) after 4 weeks of medication.
OtherMean change in blood glucoseFour weeksMean change (from baseline) in blood glucose after 4 weeks of medication.

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

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.

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