Evidence map›Paper›PMID 30354703›Full record

Trial reportHypertension (Dallas, Tex. : 1979)2018

Randomized Crossover Trial of the Impact of Morning or Evening Dosing of Antihypertensive Agents on 24-Hour Ambulatory Blood Pressure.

Neil R Poulter, Christos Savopoulos, Aisha Anjum, Martha Apostolopoulou, Neil Chapman, Mary Cross, Emanuela Falaschetti, Spiros Fotiadis, Rebecca M James, Ilias Kanellos and 5 more

Registry-linked trialOpen access · bronzeAbstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Hypertension (Dallas, Tex. : 1979), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01669928 (Hellenic Anglo Research Into Morning Or Evening Antihypertensive Drug deliverY Trial), which is not on this map. Cited by 31 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 2 pooled it
5.5field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01669928 phase4completednot on this map

Hellenic Anglo Research Into Morning Or Evening Antihypertensive Drug deliverY Trial

TypeinterventionalSponsorImperial College LondonRan2012 to 2015Enrolled103ConditionsHypertensionArmsAnti-hypertensive Medication -
3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 2 syntheses or guidelines pooled it, 81 citations in OpenAlex.

  1. Chronotherapy for Hypertension: A Meta-Analysis and Systematic Review of RCTs.American journal of cardiovascular drugs : drugs, devices, and other interventions · 2025
    Pooled it
  2. Evening versus morning dosing regimen drug therapy for hypertension.The Cochrane database of systematic reviews · 2024
    Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. The Japanese Society of Hypertension Guidelines for the management of elevated blood pressure and hypertension 2025 (JSH2025).Hypertension research : official journal of the Japanese Society of Hypertension · 2026
    Article
  8. Review
  9. Review
  10. Prognostic value of nighttime blood pressure in patients with chronic kidney disease.Hypertension research : official journal of the Japanese Society of Hypertension · 2025
    Article
  11. Article
  12. Observational
  13. Review
  14. Demonstrating the Benefits of Antihypertensive Nighttime Dosing and Indapamide Usage in Hypertension Management.The Journal of pharmacy technology : jPT : official publication of the Association of Pharmacy Technicians · 2024
    Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Circadian rhythms and renal pathophysiology.The Journal of clinical investigation · 2022
    Review
  20. Pharmacotherapy for Essential Hypertension: A Brief Review.Methodist DeBakey cardiovascular journal · 2022
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 2 institutions in 2 countries.

Neil R PoulterFrom the Imperial Clinical Trials Unit (N.R.P, A.A, M.C, E.F, M.S.), Imperial College London, United Kingdom, 1st Medical Propaedeutic Department, Aristotle University, Thessaloniki, Greece.
Christos SavopoulosImperial College London, United Kingdom, 1st Medical Propaedeutic Department, Aristotle University, Thessaloniki, Greece (C.S., M.A., S.F., I.K., A.I.H.).
Aisha AnjumFrom the Imperial Clinical Trials Unit (N.R.P, A.A, M.C, E.F, M.S.), Imperial College London, United Kingdom, 1st Medical Propaedeutic Department, Aristotle University, Thessaloniki, Greece.
Martha ApostolopoulouImperial College London, United Kingdom, 1st Medical Propaedeutic Department, Aristotle University, Thessaloniki, Greece (C.S., M.A., S.F., I.K., A.I.H.).
Neil ChapmanNHLI (P.S, D.T, N.C, S.T.), Imperial College London, United Kingdom, 1st Medical Propaedeutic Department, Aristotle University, Thessaloniki, Greece.
Mary CrossFrom the Imperial Clinical Trials Unit (N.R.P, A.A, M.C, E.F, M.S.), Imperial College London, United Kingdom, 1st Medical Propaedeutic Department, Aristotle University, Thessaloniki, Greece.
Emanuela FalaschettiFrom the Imperial Clinical Trials Unit (N.R.P, A.A, M.C, E.F, M.S.), Imperial College London, United Kingdom, 1st Medical Propaedeutic Department, Aristotle University, Thessaloniki, Greece.
Spiros FotiadisImperial College London, United Kingdom, 1st Medical Propaedeutic Department, Aristotle University, Thessaloniki, Greece (C.S., M.A., S.F., I.K., A.I.H.).
Rebecca M JamesWilliam Harvey Clinical Research Centre, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, United Kingdom (R.M.J.).
Ilias KanellosImperial College London, United Kingdom, 1st Medical Propaedeutic Department, Aristotle University, Thessaloniki, Greece (C.S., M.A., S.F., I.K., A.I.H.).
Matyas SzigetiFrom the Imperial Clinical Trials Unit (N.R.P, A.A, M.C, E.F, M.S.), Imperial College London, United Kingdom, 1st Medical Propaedeutic Department, Aristotle University, Thessaloniki, Greece.
Simon ThomNHLI (P.S, D.T, N.C, S.T.), Imperial College London, United Kingdom, 1st Medical Propaedeutic Department, Aristotle University, Thessaloniki, Greece.
Peter SeverNHLI (P.S, D.T, N.C, S.T.), Imperial College London, United Kingdom, 1st Medical Propaedeutic Department, Aristotle University, Thessaloniki, Greece.
David ThompsonNHLI (P.S, D.T, N.C, S.T.), Imperial College London, United Kingdom, 1st Medical Propaedeutic Department, Aristotle University, Thessaloniki, Greece.
Apostolos I HatzitoliosImperial College London, United Kingdom, 1st Medical Propaedeutic Department, Aristotle University, Thessaloniki, Greece (C.S., M.A., S.F., I.K., A.I.H.).
Imperial College London · GBAristotle University of Thessaloniki · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Some data suggest that nocturnal dosing of antihypertensive agents may reduce cardiovascular outcomes more than daytime dosing. This trial was designed to evaluate whether ambulatory blood pressure monitoring levels differ by timing of drug dosing. Patients aged 18 to 80 years with reasonably controlled hypertension (≤150/≤90 mm Hg) on stable therapy of ≥1 antihypertensive agent were recruited from 2 centers in London and Thessaloniki. Patients were randomized to receive usual therapy either in the morning (6 am-11 am) or evening (6 pm-11 pm) for 12 weeks when participants crossed over to the alternative timing for a further 12 weeks. Clinic blood pressures and a 24-hour recording were taken at baseline, 12, and 24 weeks and routine blood tests were taken at baseline. The study had 80% power to detect 3 mm Hg difference in mean 24-hour systolic blood pressure (α=0.05) by time of dosing. A 2-level hierarchical regression model adjusted for center, period, and sequence was used. Of 103 recruited patients (mean age, 62; 44% female), 95 patients (92%) completed all three 24-hour recordings. Mean 24-hour systolic and diastolic blood pressures did not differ between daytime and evening dosing. Similarly, morning and evening dosing had no differential impact on mean daytime (7 am-10 pm) and nighttime (10 pm-7 am) blood pressure levels nor on clinic levels. Stratification by age (≤65/≥65 years) or sex did not affect results. In summary, among hypertensive patients with reasonably well-controlled blood pressure, the timing of antihypertensive drug administration (morning or evening) did not affect mean 24-hour or clinic blood pressure levels. Clinical Trial Registration- URL: http://www.clinicaltrials.gov . Unique identifier: NCT01669928.

Indexed as

Antihypertensive AgentsDose-Response Relationship, DrugDrug Administration ScheduleHypertensionAgedBlood PressureBlood Pressure Monitoring, AmbulatoryDouble-Blind MethodDrug MonitoringFemaleHumansMaleMiddle AgedTreatment OutcomeAntihypertensive Agentsambulatory blood pressureantihypertensive agentsdosing timeshypertensionrandomized trial

Identifiers

PMID30354703
OpenAlexW2889497668

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.