Evidence map›Paper›PMID 37745092›Full record

ArticleFrontiers in cardiovascular medicine2023

A randomized control trial to assess optical coherence tomography parameters of the Xlimus drug-eluting stent: the XLIMIT trial.

Luca Testa, Mattia Squillace, Nicoletta Ventrella, Raul Moreno, Santiago Jiménez-Valero, Antoni Serra, Joan Antoni Gomez Hospital, Michele Bellamoli, Antonio Popolo Rubbio, Francesco Bedogni

Registry-linked trialAbstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03745053 (XLIMus Drug Eluting Stent), which is not on this 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.

NCT03745053 nacompletednot on this map

XLIMus Drug Eluting Stent: a randomIzed Controlled Trial to Assess Endothelization

TypeinterventionalSponsorCardionovum GmbHRan2019 to 2023Enrolled180ConditionsCoronary Artery DiseaseArmsXlimus DES Implantation during coronary angioplasty, Synergy DES Implantation during coronary angioplasty
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

10 authors.

Luca Testa *Department of Cardiology, IRCCS Policlinico S. Donato, Milan, Italy.
Mattia Squillace *Department of Cardiology, IRCCS Policlinico S. Donato, Milan, Italy.
Nicoletta VentrellaDepartment of Cardiology, IRCCS Policlinico S. Donato, Milan, Italy.
Raul MorenoDepartment of Cardiology, Hospital La Paz, IdiPAZ, Madrid, Spain.
Santiago Jiménez-ValeroDepartment of Cardiology, Hospital La Paz, IdiPAZ, Madrid, Spain.
Antoni SerraDepartment of Cardiology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Joan Antoni Gomez HospitalDepartment of Cardiology, Hospital Bellvitge, Barcelona, Spain.
Michele BellamoliDepartment of Cardiology, Fondazione Poliambulanza, Brescia, Italy.
Antonio Popolo RubbioDepartment of Cardiology, IRCCS Policlinico S. Donato, Milan, Italy.
Francesco BedogniDepartment of Cardiology, IRCCS Policlinico S. Donato, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Third generation drug-eluting stents (DES) potentially offer better technical performance and reduced neointimal proliferation than previous generation DES. The XLIMIT non-inferiority trial evaluated the performance of the Xlimus (a novel sirolimus-eluting coronary stent system) in terms of endothelialization and tissue healing compared to the bioresorbable polymer Synergy DES. Methods: A total of 177 patients undergoing percutaneous coronary intervention (PCI) were randomized in a 2:1 ratio (2 Xlimus: 1 Synergy). The primary endpoints, defined as the in-stent neointimal volume weighted by the sum of the lengths of the implanted stent (ISNV) and the in-stent neointimal percent volume obstruction (%VO) were evaluated at 6-9 months by means of optical coherence tomography (OCT). Additional OCT parameters as well as clinical endpoints were also collected. Results: Most of the patients were males (77.4%), and the mean age was 64 years. One third of the population had stable angina/silent ischemia. A total of 300 stents (237 lesions) were analyzed: 198 (152 lesions) were in the Xlimus group, and 102 (85 lesions) in the Synergy group. The ISNV in the Xlimus group was 30.7 ± 24.5 mm Conclusions: The study results confirm that the biological interaction of the Xlimus and Synergy DES with the coronary artery is comparable, and that translates in very reassuring OCT parameters at follow-up: as such, the Xlimus is non-inferior to the Synergy. Clinical Trial Registration: ClinicalTrials.gov, identifier (NCT03745053).

Indexed as

endothelialization third generation DESneointimal volumeOCTrestenosisthird generation DES

Identifiers

PMID37745092
PMCPMC10511894

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