Evidence map›Paper›PMID 32357559›Full record

ArticleJournal of clinical medicine2020

Efficacy and Safety of a 0.1% Tacrolimus Nasal Ointment as a Treatment for Epistaxis in Hereditary Hemorrhagic Telangiectasia: A Double-Blind, Randomized, Placebo-Controlled, Multicenter Trial.

Sophie Dupuis-Girod, Anne-Emmanuelle Fargeton, Vincent Grobost, Sophie Rivière, Marjolaine Beaudoin, Evelyne Decullier, Lorraine Bernard, Valentine Bréant, Bettina Colombet, Pierre Philouze and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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.

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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Hereditary haemorrhagic telangiectasia.Nature reviews. Disease primers · 2025
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. 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

13 authors at 6 institutions in 1 country.

Sophie Dupuis-GirodHospices Civils de Lyon, Hôpital Femme-Mère-Enfants, Service de Génétique et Centre de Référence de la Maladie de Rendu-Osler, F-69677 Bron, France.ORCID 0000-0002-8834-5526
Anne-Emmanuelle FargetonHospices Civils de Lyon, Hôpital Femme-Mère-Enfants, Service de Génétique et Centre de Référence de la Maladie de Rendu-Osler, F-69677 Bron, France.
Vincent GrobostService de Médecine Interne, CHU Estaing, 63100 Clermont-Ferrand, France.
Sophie RivièreService de Médecine Interne CHU de Montpellier, Hôpital St Eloi, and Centre d'Investigation Clinique, Inserm, CIC 1411, F-34295 Montpellier CEDEX 7, France.
Marjolaine BeaudoinHospices Civils de Lyon, Hôpital Femme-Mère-Enfants, Service de Génétique et Centre de Référence de la Maladie de Rendu-Osler, F-69677 Bron, France.
Evelyne DecullierHospices Civils de Lyon, Pôle Santé Publique, F-69003 Lyon, France.ORCID 0000-0002-2412-4767
Lorraine BernardHospices Civils de Lyon, Pôle Santé Publique, F-69003 Lyon, France.
Valentine BréantHospices Civils de Lyon, Pharmacie, Hôpital Louis Pradel, F-69677 Bron, France.
Bettina ColombetHospices Civils de Lyon, Pharmacie, Hôpital Louis Pradel, F-69677 Bron, France.
Pierre PhilouzeHospices Civils de Lyon, Hôpital de la Croix Rousse, Service ORL, F-69317 Lyon, France.
Sabine BaillyInserm, CEA, Laboratory Biology of Cancer and Infection, University, Grenoble Alpes, F-38000 Grenoble, France.
Frédéric FaureHospices Civils de Lyon, Hôpital E. Herriot, Service ORL, F-69437 Lyon, France.
Ruben HermannHospices Civils de Lyon, Hôpital E. Herriot, Service ORL, F-69437 Lyon, France.ORCID 0000-0002-1920-6450
Hospices Civils de Lyon · FRInserm · FRHôpital Femme Mère Enfant · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRHôpital de la Croix-Rousse · FRUniversité Claude Bernard Lyon 1 · FR

Funding

Ministère de l'Education Nationale, de l'Enseignement Superieur et de la Recherche PHRC 2016undefined <span style="color:gray;font-size:10px;">undefined</span> AMRO
6 · The paper itself

Abstract

Hereditary hemorrhagic telangiectasia is a rare but ubiquitous genetic disease. Epistaxis is the most frequent and life-threatening manifestation and tacrolimus, an immunosuppressive agent, appears to be an interesting new treatment option because of its anti-angiogenic properties. Our objective was to evaluate, six weeks after the end of the treatment, the efficacy on the duration of nosebleeds of tacrolimus nasal ointment, administered for six weeks to patients with hereditary hemorrhagic telangiectasia complicated by nosebleeds, and we performed a prospective, multicenter, randomized, placebo-controlled, double-blinded, ratio 1:1 phase II study. Patients were recruited from three French Hereditary Hemorrhagic Telangiectasia (HHT) centers between May 2017 and August 2018, with a six-week follow-up, and we included people aged over 18 years, diagnosed with hereditary hemorrhagic telangiectasia and epistaxis (total duration > 30 min/6 weeks prior to inclusion). Tacrolimus ointment 0.1% was self-administered by the patients twice daily. About 0.1 g of product was to be administered in each nostril with a cotton swab. A total of 50 patients was randomized and treated. Mean epistaxis duration before and after treatment in the tacrolimus group were 324.64 and 249.14 min, respectively, and in the placebo group 224.69 and 188.14 min, respectively. Epistaxis duration improved in both groups, with no significant difference in our main objective comparing epistaxis before and after treatment (

Indexed as

epistaxisgenetic diseasehereditary hemorrhagic telangiectasianasal ointmentnosebleedsrare diseasetacrolimus

Identifiers

PMID32357559
PMCPMC7287684
OpenAlexW3019224115

What OpenQuestion 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 OpenQuestion graph.