Evidence mapPaperPMID 39499552Full record

ArticlePain2025

Widespread pain phenotypes impact treatment efficacy results in randomized clinical trials for interstitial cystitis/bladder pain syndrome: a Multidisciplinary Approach to the Study of Chronic Pelvic Pain network study.

John T Farrar, Kenneth T Locke, J Quentin Clemens, James W Griffith, Steven E Harte, Ziya Kirkali, Karl J Kreder, John N Krieger, H Henry Lai, Robert M Moldwin and 11 more

Abstract read
In one paragraph

Article in Pain, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors.

John T FarrarDepartment of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.ORCID 0000-0001-8656-5157
Kenneth T LockeDepartment of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
J Quentin ClemensDepartment of Urology, University of Michigan Medical School, Ann Arbor, MI, United States.ORCID 0000-0002-0759-3385
James W GriffithDepartment of Medical Social Sciences, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States.ORCID 0000-0002-4840-8692
Steven E HarteDepartment of Anesthesiology, University of Michigan Medical School, Ann Arbor, MI, United States.ORCID 0000-0002-2929-8694
Ziya KirkaliNational Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD, United States.ORCID 0000-0002-2918-4347
Karl J KrederDepartment of Urology, Roy J and Lucille A Carver College of Medicine, The University of Iowa, Iowa City, IA, United States.ORCID 0000-0002-8981-5286
John N KriegerDepartment of Urology, University of Washington School of Medicine, Seattle, WA, United States.ORCID 0000-0003-4111-3442
H Henry LaiDepartment of Urology, Washington University School of Medicine, St. Louis, MO, United States.ORCID 0000-0003-2691-994
Robert M MoldwinDepartment of Urology, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Lake Success, NY, United States.ORCID 0000-0002-2603-9160
Chris MullinsNational Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD, United States.ORCID 0000-0003-1559-852
Bruce D NaliboffDepartment of Psychiatry and Biobehavioral Sciences, David Geffen School of Medicine, University of California, Los Angeles, CA, United States.ORCID 0000-0003-0959-8670
Michel A PontariDepartment of Urology, Lewis Katz School of Medicine, Temple University, Philadelphia, PA, United States.
Larissa V RodríguezDepartment of Urology, New York-Presbyterian/Weill Cornell Medical Center, New York, NY, United States.
Anthony J SchaefferDepartment of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States.
Andrew SchrepfDepartment of Anesthesiology, University of Michigan Medical School, Ann Arbor, MI, United States.ORCID 0000-0003-4291-0320
Alisa Stephens-ShieldsDepartment of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.ORCID 0000-0001-5422-7065
Siobhan SutcliffeDepartment of Surgery, Washington University School of Medicine, St. Louis, MO, United States.ORCID 0000-0002-4613-8107
Bayley J TapleDepartment of Psychiatry and Behavioral Sciences, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States.ORCID 0000-0002-5812-5848
David A WilliamsDepartment of Psychology, University of Michigan Medical School, Ann Arbor, MI, United States.
J Richard LandisDepartment of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.ORCID 0000-0001-8099-0988

Funding

NIDDK NIH HHS U24 DK082316NIDDK NIH HHS U24-DK082316
6 · The paper itself

Abstract

abstractPain clinical trials are notoriously complex and often inefficient in demonstrating efficacy, even for known efficacious treatments. A major issue is the difficulty in the a priori identification of specific phenotypes to include in the study population. Recent work has identified the extent of widespread pain as an important determinant of the likelihood of response to therapy, but it has not been tested in clinical trials for the treatment of interstitial cystitis/bladder pain syndrome (IC/BPS). We explored this hypothesis using data from 3 previously published trials testing treatments for IC/BPS, which suggested modest benefits but did not meet a priori primary outcome statistical significance criteria. Importantly, these studies also collected symptom questionnaire data that allowed us to retrospectively identify participants with and without widespread pain. Analyzing the treatment by the degree of widespread pain revealed a difference in outcome and statistical significance level for each trial. Participants with predominately local pain (ie, limited widespread pain symptoms) responded to therapy targeting local symptoms, whereas those with widespread pain did not. Alternatively, participants with widespread pain beyond their local pelvic pain responded to more centrally acting treatments. Our results suggest that differentiating patients based on widespread vs more localized pain is a key consideration for designing future clinical trials for conditions with variable pain profiles, such as IC/BPS and potentially other pain-based syndromic disorders.

Indexed as

Chronic PainCystitis, InterstitialPelvic PainRandomized Controlled Trials as TopicAdultAgedFemaleHumansMaleMiddle AgedPain MeasurementPhenotypeRetrospective StudiesTreatment OutcomeInterstitial cystitisPain measurementPelvic painReanalysis of clinical trial resultsWidespread pain

Identifiers

PMID39499552
PMCPMC12004979

What Socratic holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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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.