Evidence map›Paper›PMID 41408649›Full record

ArticleTrials2025

The Antibiotic effect of Silver CAPD Catheter on Peritoneal Dialysis-related infections (ASCA-PD) study: a multicenter randomized open-label trial protocol.

Masahiro Eriguchi, Yasuhiko Ito, Hisako Yoshida, Masaru Matsui, Takaaki Kosugi, Ai Nagashima, Genri Tagami, Shohei Yamada, Tsutomu Sakurada, Masahiro Nakagaki and 21 more

Abstract readClinical Trial Protocol
In one paragraph

Article in Trials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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0 citing papers in PubMed.

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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

31 authors.

Masahiro EriguchiDepartment of Nephrology, Nara Medical University, Kashihara, Japan.
Yasuhiko ItoDepartment of Nephrology and Rheumatology, Aichi Medical University, Nagakute, Japan. yasuito57@aichi-med-u.ac.jp.
Hisako YoshidaDepartment of Medical Statistics, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Masaru MatsuiDepartment of Nephrology, Nara Medical University, Kashihara, Japan.
Takaaki KosugiDepartment of Nephrology, Nara Medical University, Kashihara, Japan.
Ai NagashimaDepartment of Nephrology and Rheumatology, Aichi Medical University, Nagakute, Japan.
Genri TagamiDepartment of Nephrology and Rheumatology, Aichi Medical University, Nagakute, Japan.
Shohei YamadaDivision of Nephrology and Hypertension, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan.
Tsutomu SakuradaDivision of Nephrology and Hypertension, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan.
Masahiro NakagakiDivision of Nephrology, Kokura Memorial Hospital, Kitakyushu, Japan.
Kenji HaradaDivision of Nephrology, Kokura Memorial Hospital, Kitakyushu, Japan.
Satoshi KurahashiDepartment of Nephrology, Kansai Electric Power Hospital, Osaka, Japan.
Naohiro TodaDepartment of Nephrology, Kansai Electric Power Hospital, Osaka, Japan.
Satoshi OtotakeDepartment of Renal Replacement Therapy, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Masashi MizunoDepartment of Renal Replacement Therapy, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Hiroyuki KadoyaDepartment of General Geriatric Medicine, Kawasaki Medical School, Kurashiki, Japan.
Seiji KishiDepartment of Nephrology and Hypertension, Kawasaki Medical School, Kurashiki, Japan.
Shunnosuke KunokiDepartment of Endocrinology, Metabolism and Nephrology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Yukinao SakaiDepartment of Endocrinology, Metabolism and Nephrology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Yuichi SatoDepartment of Nephrology, Shinshu University School of Medicine, Matsumoto, Japan.
Koji HashimotoDepartment of Nephrology, Shinshu University School of Medicine, Matsumoto, Japan.
Masatoshi MatsunamiDepartment of Nephrology, Kameda Medical Center, Kamogawa, Japan.
Tomo SuzukiDepartment of Nephrology, Kameda Medical Center, Kamogawa, Japan.
Shunsuke TakahashiDepartment of Nephrology, National Hospital Organization Kure Medical Center, Kure, Japan.
Kenji NakataDepartment of Nephrology and Dialysis, Saiseikai Yokohamashi Tobu Hospital, Yokohama, Japan.
Kiyoto KoibuchiDepartment of Nephrology and Dialysis, Saiseikai Yokohamashi Tobu Hospital, Yokohama, Japan.
Hideaki OkaDivision of Kidney Center, Matsuyama Red Cross Hospital, Matsuyama, Japan.
Taro KamimuraDivision of Kidney Center, Matsuyama Red Cross Hospital, Matsuyama, Japan.
Hidenobu MatsumotoDivision of Nephrology, Tagawa Municipal Hospital, Tagawa, Japan.
Takeshi YoshidaDivision of Nephrology, Tagawa Municipal Hospital, Tagawa, Japan.
Kazuhiko TsuruyaDepartment of Nephrology, Nara Medical University, Kashihara, Japan.

Funding

Clinical Research Grant Program at Nara Medical University JHR2400003the Public Research Grant from the Japanese Association of Dialysis Physicians JADP grant 2024-8
6 · The paper itself

Abstract

backgroundPeritoneal dialysis (PD) offers greater flexibility than hemodialysis, especially in patients with limited mobility or demanding schedules; however, PD-related infection is a major complication and a cause of withdrawal from peritoneal dialysis. The Antibiotic effect of Silver continuous ambulatory peritoneal dialysis (CAPD) Catheter on Peritoneal Dialysis-related infections (ASCA-PD) study will evaluate the effectiveness of a novel silver CAPD catheter, incorporating silver-based antimicrobial technology, for preventing these infections and improving PD adherence. METHODS/

designThis randomized, open-label, parallel-group, multicenter trial will evaluate the efficacy and safety of a silver CAPD catheter compared with those of a conventional catheter at 14 Japanese facilities. A total of 250 adult patients with newly initiated PD will be enrolled and randomized 1:1 to receive either catheter type. The key exclusion criteria are prior PD, emergency PD initiation, non-abdominal exit-site placement, metal allergy, life expectancy <1 year, severe liver disease, certain dermatologic conditions, and immunosuppression. After providing informed consent, patients will undergo nasal swab screening for methicillin-resistant Staphylococcus aureus. Randomization will be stratified by facility and diabetes status. The primary outcome is the composite endpoint of all exit-site and tunnel infections within 12 months of PD initiation. Secondary outcomes include individual infection events, catheter removal, peritonitis, catheter patency, allergic reactions, technique failure (transition to hemodialysis for ≥30 days or death), and transition to hybrid dialysis. A Poisson regression model will be used to analyze the primary outcome, adjusting for observation time, treatment group, and stratification factors. Time-to-event secondary outcomes will be analyzed by competing risk regression. Subgroup analyses will be carried out to explore the impacts of age, sex, diabetes, insertion method, and body mass index. DISCUSSION: Unlike previous designs, our silver CAPD catheter incorporates AgNPs into silicone, enabling sustained antimicrobial effects both externally and internally, potentially overcoming limitations seen in prior human studies. This study will demonstrate the efficacy of silver CAPD catheters for preventing PD-related infections, especially during the initiation phase of PD, with the aim of providing a new therapeutic option.

trial registrationJapan Registry of Clinical Trials, jRCTs052250003. Registered on April 4, 2025.

Indexed as

Anti-Bacterial AgentsCatheter-Related InfectionsCatheters, IndwellingPeritoneal Dialysis, Continuous AmbulatoryPeritonitisSilverAdultEquipment DesignFemaleHumansJapanMaleMethicillin-Resistant Staphylococcus aureusMulticenter Studies as TopicRandomized Controlled Trials as TopicTreatment OutcomeAnti-Bacterial AgentsSilverExit-site infectionPD-related infectionsPD-related peritonitisPeritoneal dialysisPreventionRandomized controlled trialSilver CAPD catheter

Identifiers

PMID41408649
PMCPMC12821953

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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 OpenQuestion graph.