Evidence map›Paper›PMID 27015224›Full record

Trial reportMedicine2016

Combination With Low-dose Dextromethorphan Improves the Effect of Amlodipine Monotherapy in Clinical Hypertension: A First-in-human, Concept-proven, Prospective, Dose-escalation, Multicenter Study.

Wei-Hsian Yin, Pei Chen, Hung-I Yeh, Kuo-Yang Wang, Yi-Jen Hung, Wei-Kung Tseng, Ming-Shien Wen, Tao-Cheng Wu, Chau-Chung Wu, Shu-Meng Cheng and 1 more

Open access · goldAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 39% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Novel Approaches to Restore Pancreatic Beta-Cell Mass and Function.Handbook of experimental pharmacology · 2022
    Review
  3. Redox Regulation of Inflammatory Processes Is Enzymatically Controlled.Oxidative medicine and cellular longevity · 2017
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Wei-Hsian YinFrom the Heart Center, Cheng-Hsin General Hospital (W-HY); Faculty of Medicine, National Yang-Ming University (W-HY); Institute of Pharmacology, National Yang-Ming University (J-WC); TSH Biopharm Corporation Ltd (PC); Department of Medicine, Mackay Memorial Hospital, Taipei (H-IY); Division of Cardiology, Taichung Veterans General Hospital (K-YW); Department of Internal Medicine, Chung San Medical University, Taichung (K-YW); Division of Endocrinology and Metabolism (Y-JH); Division of Cardiology, Tri-Service General Hospital, Taipei (S-MC); Department of Cardiology, E-DA Medical University Hospital, Kaohsiung (W-KT); Department of Cardiology, Chang Gung Memorial Hospital Linkou, Taoyuan (M-SW); Division of Cardiology, Taipei Veterans General Hospital (T-CW, J-WC); Department of Internal Medicine, National Taiwan University Hospital (C-CW); and Department of Medical Research, Taipei Veterans General Hospital, Taipei, Taiwan, ROC (J-WC).
Pei Chen
Hung-I Yeh
Kuo-Yang Wang
Yi-Jen Hung
Wei-Kung Tseng
Ming-Shien Wen
Tao-Cheng Wu
Chau-Chung Wu
Shu-Meng Cheng
Jaw-Wen Chen
Tri-Service General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The combination of low rather than high dose of dextromethorphan (DXM) with amlodipine (AM) could improve blood pressure (BP) reduction in hypertensive animals. The study aimed to evaluate the feasibility of different doses of DXM combined with standard AM treatment in clinical hypertension.This was a prospective, 14-week, dose-escalation, multicenter study. After 2-week run-in period with AM 5 mg/day, hypertensive patients who got the BP goal of 140/90 mmHg kept receiving AM monotherapy for another 12 weeks. The nonresponders, while kept on AM 5 mg/day, received additional DXM treatment for 3 sequential dose-titrated periods with initially 2.5 mg/day, followed by 7.5 mg/day, and finally 30 mg/day. Each period was for 4 weeks. The patients at BP goal after each treatment period were defined as the responders and kept on the same combination till the end of the study. The responder rate of each treatment period was recorded. The changes of BP and serum antioxidant/endothelial markers between week 14 and week 2 were evaluated.Of the 103 patients initially enrolled, 89 entered the treatment period. In the 78 patients completing the study, 31 (40%) at BP goal after 2-week AM run-in kept on AM monotherapy (DXM0). The addition of 2.5 (DXM2.5) and 7.5 mg/day (DXM7.5) of DXM enabled BP goal achievement in 22 (47%) nonresponders to AM monotherapy including 16 (29%) with DXM2.5 and 6 (18%) with DXM7.5. Only 4 patients (16%) reached BP goal with the combination of DXM 30 mg/day (DXM30). Overall, 73% of the 78 patients reached BP goal at the end of the 14-week study. Mean systolic BP was reduced by 7.9% ± 7.0% with DXM2.5 (P < 0.001) and by 5.4% ± 2.4% with DXM7.5 (P = 0.003) respectively at week 14 from that at week 2, which was unchanged in either DXM0 or DXM30 group. Besides, the effects of combination treatment were particularly significant in the patients with impaired endothelial function suggested by reduced serum NOx level at baseline.Accordingly, the combination with low dose of DXM was feasible to improve BP control in patients who failed to achieve the BP goal by standard AM monotherapy. The benefit effects might be significant especially in patients with impaired endothelial function.

Indexed as

AmlodipineAntihypertensive AgentsDextromethorphanDrug Therapy, CombinationFemaleHumansHypertensionMaleMiddle AgedProspective StudiesSingle-Blind MethodAmlodipineAntihypertensive AgentsDextromethorphan

Identifiers

PMID27015224
PMCPMC4998419
OpenAlexW2325863124

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.