Evidence map›Paper›PMID 39440727›Full record

Trial reportCurrent vascular pharmacology2025

Efficacy and Safety of Sarpogrelate on Symptom Improvement in Patients with Peripheral Arterial Disease (PAD) and/or Being at Risk of PAD: A Single Arm, Multi-Centered, Open-Label Trial.

Jong Chul Won, Tae-Jin Song, Jae Hyoung Park, Hee-Tae Kim, Kyong Hoon Lee, Keun Yong Park, Ho-Seung Jeong, Ung Jeon, Kyung Wan Min, Soo Lim

Abstract readMulticenter StudyClinical Trial
PubMed Publisher
In one paragraph

Trial report in Current vascular pharmacology, 2025. 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

10 authors.

Jong Chul WonDepartment of Internal Medicine, Inje University Sanggye Paik Hospital, Korea, South.ORCID 0000-0002-2219-4083
Tae-Jin SongDepartment of Neurology, Seoul Hospital, Ewha Womans University College of Medicine, Korea, South.
Jae Hyoung ParkDepartment of Internal Medicine, Korea University Medical Center, Korea, South.
Hee-Tae KimDepartment of Neurology, Hanyang University Seoul Hospital, Korea, South.
Kyong Hoon LeeDepartment of Internal Medicine, Gachon University Gil Medical Center, Korea, South.
Keun Yong ParkDepartment of Internal Medicine, Konyang University Hospital, Korea, South.
Ho-Seung JeongDepartment of Orthopaedic Surgery, Chungbuk National University Hospital, Korea, South.
Ung JeonDepartment of Internal Medicine, Soonchunhyang University Hospital, Korea, South.
Kyung Wan MinDepartment of Internal Medicine, Eulji General Hospital, Korea, South.
Soo LimDepartment of Internal Medicine, Seoul National University College of Medicine and Seoul National University Bundang Hospital, Korea, South.ORCID 0000-0002-4137-1671

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsTo assess the efficacy and safety of sarpogrelate (300 mg) for symptom improvement in patients having peripheral arterial disease (PAD) and/or being at risk of PAD in clinical practice using the Peripheral Artery Questionnaire (PAQ).

backgroundSymptomatic changes with antiplatelets in patients with PAD are limited.

objectiveTo determine the effect and safety of sarpogrelate on the PAQ at 24 weeks from baseline.

methodsA total of 1003 patients having PAD and/or being at risk of PAD from 17 tertiary hospitals in South Korea who were treated with sarpogrelate, were enrolled in this study. PAQs were collected at baseline and at 12 and 24 weeks, together with physical examination and vital signs measurements. Lifestyle pattern was also investigated.

resultsThe average PAQ Summary Score in the efficacy evaluation analysis group significantly improved from 62.9 ± 23.7 at baseline to 68.9 ± 21.7 at 24 weeks (P<0.0001). Physical limitation items significantly improved from 69.5 ± 30.0 at baseline to 72.9 ± 28.3 after 24 weeks (P=0.0011). Symptom stability also significantly improved from 52.1 ± 21.6 at baseline to 63.6 ± 22.9 after 24 weeks (P<0.0001). Symptoms, treatment satisfaction, quality of life, and social limitation domains all improved after treatment. A total of 201 patients reported adverse events (20.0%), not directly associated with treatment.

conclusionTreatment with 300 mg (orally) of sarpogrelate demonstrated statistically significant improvements in all domains and for the summary score of the PAQ at 24 weeks, it gave good results in terms of safety. Sarpogrelate may be helpful in reducing symptoms related to PAD.

Indexed as

Peripheral Arterial DiseaseSuccinatesAgedFemaleHumansMaleMiddle AgedQuality of LifeRepublic of KoreaRisk FactorsSurveys and QuestionnairesTime FactorsTreatment OutcomesarpogrelateSuccinates5-HT2A receptorankle-brachial Indexefficacy evaluation analysis group.peripheral arterial diseaseperipheral artery questionnaireSarpogrelate

Identifiers

PMID39440727

What OpenQuestion holds

Textmetadata
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.