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Phase 4 Completed N=103 Randomized Treatment

Anti-hypertensive Medication Dosing Regimen in Effective Blood Pressure Control

Source: ClinicalTrials.gov NCT01669928 ↗
Enrolled (actual)
103
Serious AEs
1.6%
Results posted
Mar 2021
Primary outcomePrimary: Changes in 24 Hour Systolic Blood Pressure — 129.65; 129.75 mm Hg
◆ Published Evidence
Established
82citations · ~10 / year
Randomized Crossover Trial of the Impact of Morning or Evening Dosing of Antihypertensive Agents on 24-Hour Ambulatory Blood Pressure.
Hypertension (Dallas, Tex. : 1979) · 2018 · Open access · Likely link

Summary

A randomised crossover trial of anti-hypertensive medication dosing regimen in effective blood pressure control. To investigate whether there is a difference in 24 hour blood pressure (BP) control when antihypertensive medications are taken in the morning compared with the evening.

Linked Publications

  • Randomized Crossover Trial of the Impact of Morning or Evening Dosing of Antihypertensive Agents on 24-Hour Ambulatory Blood Pressure.
    Hypertension (Dallas, Tex. : 1979) · 2018 · 82 citations · Open access · Likely link

Outcome Measures

OutcomeResultp-value
PRIMARY
Changes in 24 Hour Systolic Blood Pressure
129.65; 129.75
SECONDARY
Mean Day-time ABPM Systolic BP
132.24; 132.77
SECONDARY
Mean Day-time ABPM Diastolic BP
79.27; 80.55
SECONDARY
Μean Night Time ABPM Systolic BP
122.76; 121.08
SECONDARY
Μean Night Time ABPM Diastolic BP
70.92; 70.57
SECONDARY
Mean Clinic - Systolic BP
129.37; 129.81
SECONDARY
Mean Clinic - Diastolic BP
77.26; 77.41
SECONDARY
Self Reported Side Effects
0; 3
SECONDARY
Quality of Life Score
84.14; 84.04

Eligibility Criteria

Inclusion Criteria

  • Caucasian patients aged 18-80 years;
  • History of any grade of hypertension for at least 1 year, including at least 3 months of constant antihypertensive medication (consisting of ≥ 1 antihypertensive drugs, each administered in one dose daily), with reasonably controlled BP (≤150/90 mmHg and ≥ 115/75 mmHg on usual medication) based on previous clinic records, in the last 3 months.

Exclusion Criteria

  • BP levels > 150/90 mmHg or 20 mm Hg drop of systolic BP or a > 10 mm Hg drop of diastolic BP or both between 1 and 3 min after standing from the sitting position.
  • Known Extreme dippers at baseline (fall of mean night time SBP > 20% of mean day time SBP)
  • Individuals with jobs which require night-time shift work.
  • Pregnant women or those planning to become pregnant.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01669928) and the linked publication. Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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