Evidence mapPaperPMID 36865104Full record

ArticleResearch square2023

Widespread Pain Phenotypes Impact Treatment Efficacy Results in Randomized Clinical Trials for Interstitial Cystitis/Bladder Pain Syndrome: A MAPP Network Study.

John Farrar, Kenneth Locke, J Clemens, James Griffith, Steven Harte, Ziya Kirkali, Karl Kreder, John Krieger, H Henry Lai, Robert Moldwin and 10 more

Open access · greenAbstract readPreprint
In one paragraph

Article in Research square, 2023. 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, 6 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 11 institutions in 1 country.

John FarrarUniversity of Pennsylvania Perelman School of Medicine.ORCID 0000-0001-8656-5157
Kenneth LockeUniversity of Pennsylvania, Perelman School of Medicine.
J ClemensUniversity of Michigan Medical School.
James GriffithNorthwestern University.
Steven HarteUniversity of Michigan.
Ziya KirkaliNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health.ORCID 0000-0002-2918-4347
Karl KrederUniversity of Iowa Carver College of Medicine.
John KriegerUniversity of Washington School of Medicine.
H Henry LaiWashington University School of Medicine.
Robert MoldwinHofstra North Shore-LIJ School of Medicine.
Chris MullinsNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health.
Bruce NaliboffUCLA.
Michel PontariTemple University Lewis Katz School of Medicine.
Larissa RodríguezNewYork-Presbyterian/Weill Cornell Medical Center.
Anthony SchaefferNorthwestern University.
Alisa Stephens-ShieldsUniversity of Pennsylvania.
Siobhan SutcliffeWashington University School of Medicine, St. Louis.ORCID 0000-0002-4613-8107
Bayley TapleNorthwestern University Feinberg School of Medicine.
David WilliamsUniversity of Michigan Medical School.ORCID 0000-0002-5052-4895
J LandisUniversity of Pennsylvania Perelman School of Medicine.ORCID 0000-0001-8099-0988
University of Michigan · USUniversity of Pennsylvania · USNational Institutes of Health · USCalifornia University of Pennsylvania · USCornell University · USHofstra University · USTemple University · USUCLA Health · USUniversity of Iowa · USUniversity of Washington · USWashington University in St. Louis · US

Funding

NIDDK NIH HHS U01 DK082344NIDDK NIH HHS U24 DK082316
6 · The paper itself

Abstract

Clinical trials of pain are notoriously difficult and inefficient in demonstrating efficacy even for known efficacious treatments. Determining the appropriate pain phenotype to study can be problematic. Recent work has identified the extend of widespread pain as an important factor in the likelihood of response to therapy, but has not been tested in clinical trials. Using data from three previously published negative studies of the treatment of interstitial cystitis/ bladder pain with data on the extent of widespread pain, we examined the response of patients to different therapies base on the amount of pain beyond the pelvis. Participants with predominately local but not widespread pain responded to therapy targeting local symptoms. Participants with widespread and local pain responded to therapy targeting widespread pain. Differentiating patients with and without widespread pain phenotypes may be a key feature of designing future pain clinical trials to demonstrate treatments that are effective versus not.

Identifiers

PMID36865104
PMCPMC9980200
OpenAlexW4321487430

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.