Evidence map›Paper›PMID 23863960›Full record

Trial reportJAMA dermatology2013

Oral antimycobacterial therapy in chronic cutaneous sarcoidosis: a randomized, single-masked, placebo-controlled study.

Wonder P Drake, Kyra Oswald-Richter, Bradley W Richmond, Joan Isom, Victoria E Burke, Holly Algood, Nicole Braun, Thyneice Taylor, Kusum V Pandit, Caroline Aboud and 4 more

Registry-linked trialOpen access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in JAMA dermatology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01074554 (Phase I/II Study of the Effects of Antibiotics on Sarcoidosis Pathogenesis), which is not on this map. Cited by 40 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 2 pooled it
5.1field-weighted citation impact, top 4% of its field
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.

NCT01074554 phase1 / phase2completednot on this map

Phase I/II Study of the Effects of Antibiotics on Sarcoidosis Pathogenesis

TypeinterventionalSponsorVanderbilt UniversityRan2010 to 2011Enrolled30ConditionsSarcoidosisArmsAntibiotic Regimen, Placebo Regimen
3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 2 syntheses or guidelines pooled it, 86 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Review
  6. Immunopathogenesis of Sarcoidosis.Seminars in respiratory and critical care medicine · 2025
    Review
  7. Review
  8. Review
  9. Infectious Complications of Pulmonary Sarcoidosis.Journal of clinical medicine · 2024
    Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Clinical phenotyping in sarcoidosis management.Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Environmental Risk Factors for Sarcoidosis.Frontiers in immunology · 2020
    Review
  19. Refractory Sarcoidosis: A Review.Therapeutics and clinical risk management · 2020
    Review
  20. Review
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

14 authors at 2 institutions in 1 country.

Wonder P DrakeDivision of Infectious Diseases, Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee2Department of Pathology, Microbiology, and Immunology, Vanderbilt University School of Medicine, Nashville, Tennessee.
Kyra Oswald-Richter
Bradley W Richmond
Joan Isom
Victoria E Burke
Holly Algood
Nicole Braun
Thyneice Taylor
Kusum V Pandit
Caroline Aboud
Chang Yu
Naftali Kaminski
Alan S Boyd
Lloyd E King
Vanderbilt University · USUniversity of Pittsburgh · US

Funding

VANDERBILT UNIVERSITY CTSA FOR PEDIATRIC RESEARCHUL1RR024975 · NCRR · VANDERBILT UNIVERSITY · PI BERNARD, GORDON RAPHAEL · 2007 to 2011
$45.7M
YOHIMBINE AS A MODEL OF ORTHOSTATIC INTOLERANCEM01RR000095 · NCRR · VANDERBILT UNIVERSITY · PI DRAKE, WONDER P. · 1985 to 2008
$38.3M
Immunobiology of Blood and Vascular Systems Training ProgramT32HL069765 · NHLBI · VANDERBILT UNIVERSITY · PI HAWIGER, JACK J · 2002 to 2016
$6.5M
Interdisciplinary Training Program in Lung ResearchT32HL094296 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Ray Stokes Peebles · 2008 to 2026
$6.3M
The Role of CD8 T Cells in Chronic Granulomatous InflammationK01HL103179 · NHLBI · VANDERBILT UNIVERSITY · PI OSWALD-RICHTER, KYRA A. · 2010 to 2014
$561k
Investigation of microbial hetergeneity to sarcoidosis and AAT clinical outcomeU01HL112694 · NHLBI · VANDERBILT UNIVERSITY · PI DRAKE, WONDER P. · 2012 to 2014
$463k
NCRR NIH HHS M01 RR000095NCRR NIH HHS UL1 RR-024975NCRR NIH HHS UL1 RR024975NHLBI NIH HHS 1K01HL103179-01NHLBI NIH HHS 5T32HL094296-04NHLBI NIH HHS K01 HL103179NHLBI NIH HHS T32 HL069765NHLBI NIH HHS T32HL069765-08NHLBI NIH HHS T32 HL094296NHLBI NIH HHS U01 HL112694NHLBI NIH HHS U01 HL112694-01
6 · The paper itself

Abstract

importanceSarcoidosis is a chronic granulomatous disease for which there are limited therapeutic options. This is the first randomized, placebo-controlled study to demonstrate that antimycobacterial therapy reduces lesion diameter and disease severity among patients with chronic cutaneous sarcoidosis.

objectiveTo evaluate the safety and efficacy of once-daily antimycobacterial therapy on the resolution of chronic cutaneous sarcoidosis lesions. DESIGN AND

participantsA randomized, placebo-controlled, single-masked trial on 30 patients with symptomatic chronic cutaneous sarcoidosis lesions deemed to require therapeutic intervention.

settingA tertiary referral dermatology center in Nashville, Tennessee.

interventionsParticipants were randomized to receive either the oral concomitant levofloxacin, ethambutol, azithromycin, and rifampin (CLEAR) regimen or a comparative placebo regimen for 8 weeks with a 180-day follow-up. MAIN OUTCOMES AND MEASURES: Participants were monitored for absolute change in lesion diameter and decrease in granuloma burden, if present, on completion of therapy. OBSERVATIONS: In the intention-to-treat analysis, the CLEAR-treated group had a mean (SD) decrease in lesion diameter of -8.4 (14.0) mm compared with an increase of 0.07 (3.2) mm in the placebo-treated group (P = .05). The CLEAR group had a significant reduction in granuloma burden and experienced a mean (SD) decline of -2.9 (2.5) mm in lesion severity compared with a decline of -0.6 (2.1) mm in the placebo group (P = .02). CONCLUSIONS AND RELEVANCE: Antimycobacterial therapy may result in significant reductions in chronic cutaneous sarcoidosis lesion diameter compared with placebo. These observed reductions, associated with a clinically significant improvement in symptoms, were present at the 180-day follow-up period. Transcriptome analysis of sarcoidosis CD4+ T cells revealed reversal of pathways associated with disease severity and enhanced T-cell function following T-cell receptor stimulation.

trial registrationclinicaltrials.gov Identifier: NCT01074554.

Indexed as

Administration, OralAdultAgedAnti-Bacterial AgentsAzithromycinCD4-Positive T-LymphocytesChronic DiseaseDrug Therapy, CombinationEthambutolFemaleFollow-Up StudiesHumansLevofloxacinMaleMiddle AgedOfloxacinAnti-Bacterial AgentsAzithromycinEthambutolLevofloxacinOfloxacinRifampin

Identifiers

PMID23863960
PMCPMC3927541
OpenAlexW1978847824

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.