Evidence mapPaperPMID 41884792Full record

ArticleTherapeutic advances in infectious disease

Symptom relief and cytokine modulation by clarithromycin in mild COVID-19 pneumonia: an exploratory, multicenter, randomized-controlled open-label trial (CAME-COVID study).

Kazuko Yamamoto, Naoki Iwanaga, Asuka Umemura, Toyomitsu Sawai, Makoto Sumiyoshi, Kohji Hashiguchi, Yusuke Mori, Hiroshi Ishii, Yoji Futsuki, Maiko Kiyohara and 16 more

Abstract read
In one paragraph

Article in Therapeutic advances in infectious disease. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

26 authors.

Kazuko YamamotoDepartment of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Nagasaki, Japan.
Naoki IwanagaDepartment of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Nagasaki, Japan.
Asuka UmemuraDepartment of Respiratory Medicine, Sasebo City General Hospital, Sasebo, Nagasaki, Japan.
Toyomitsu SawaiDepartment of Respiratory Medicine, Nagasaki Harbor Medical Center, Nagasaki, Nagasaki, Japan.
Makoto SumiyoshiDepartment of Respiratory Medicine, Japan Community Health Care Organization JCHO Isahaya General Hospital, Isahaya, Nagasaki, Japan.
Kohji HashiguchiDepartment of Respiratory Medicine, Japanese Red Cross Nagasaki Genbaku Hospital, Nagasaki, Nagasaki, Japan.
Yusuke MoriDepartment of Respiratory Medicine, Kitakyusyu City Yahata Hospital, Kitakyusyu, Fukuoka, Japan.
Hiroshi IshiiDepartment of Respiratory Medicine, Fukuoka University Chikushi Hospital, Chikushino, Fukuoka, Japan.
Yoji FutsukiDepartment of Respiratory Medicine, Saiseikai Nagasaki Hospital, Nagasaki, Nagasaki, Japan.
Maiko KiyoharaDepartment of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Nagasaki, Japan.
Kenji OtaDepartment of Laboratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Kosuke KosaiDepartment of Laboratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Daisuke SasakiDepartment of Laboratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Yuki TakamatsuDepartment of Virology, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Nagasaki, Japan.
Shingo InoueDepartment of Virology, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Nagasaki, Japan.
Kouichi MoritaDepartment of Virology, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Nagasaki, Japan.
Shin TsutsuiDepartment of Radiology, Nagasaki University Hospital, Nagasaki, Nagasaki, Japan.
Kazuto AshizawaDepartment of Clinical Oncology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Takahiro TakazonoDepartment of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Nagasaki, Japan.ORCID https://orcid.org/0000-0002-0696-5386
Noriho SakamotoDepartment of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Nagasaki, Japan.
Naoki HosogayaDepartment of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Nagasaki, Japan.
Masato TashiroInfection Control and Education Center, Department of Infectious Diseases, Nagasaki University Hospital, Nagasaki, Nagasaki, Japan.ORCID https://orcid.org/0000-0001-7609-7679
Takeshi TanakaInfection Control and Education Center, Department of Infectious Diseases, Nagasaki University Hospital, Nagasaki, Nagasaki, Japan.
Koichi IzumikawaDepartment of Infectious Diseases, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Katsunori YanagiharaDepartment of Laboratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Hiroshi MukaeDepartment of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Nagasaki, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Coronavirus disease 2019 (COVID-19) remains an epidemic worldwide, and long COVID is a major social concern. Therapeutic options for relieving symptoms of COVID-19 pneumonia are limited. Clarithromycin (CAM), a macrolide antimicrobial, also functions as an immunomodulator. Objectives: To assess the efficacy of CAM in improving clinical symptoms and attenuating inflammation in patients with mild COVID-19, with the aim of preventing progression to severe disease. Design: An exploratory, multicenter, randomized-controlled, open-label trial. Methods: This trial enrolled patients with mild COVID-19 pneumonia without oxygen supplementation from May 2021 through February 2022 in eight hospitals in Japan. Patients were randomly assigned in a 1:1:1 ratio to groups A (CAM 800 mg/day, 7 days), B (CAM 400 mg/day, 7 days), or C (standard treatment). The primary endpoint was the number of days required for 50% improvement in seven symptoms (fatigue, headache, cough, shortness of breath, taste/smell disturbance, and general unwellness) based on severity scores. Secondary endpoints included inflammatory cytokines, viral load, immunoglobulins, and pneumonia infiltrations. Results: A total of 56 patients were enrolled and randomized. The primary endpoint did not differ significantly between groups (A: 5.0 days, B: 4.0 days, C: 4.0 days), though the seven symptoms tended to disappear earlier in group A than group C ( Conclusion: CAM is safe and potentially useful for improving partial COVID-related symptoms and exerting immunomodulation during COVID-19 pneumonia. Trial registration: Japan Registry of Clinical Trials (jRCT; registration number: jRCTs071210011; https://jrct.mhlw.go.jp/latest-detail/jRCTs071210011) on April 13, 2021.

Indexed as

clarithromycincoronavirus disease 2019 (COVID-19)cytokinesfatiguelong COVIDpneumonia

Identifiers

PMID41884792
PMCPMC13009641

What Socratic holds

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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 Socratic graph.