Evidence map›Paper›PMID 39323655›Full record

Trial reportJBMR plus2024

Pamidronate for pain in adult chronic nonbacterial osteitis: protocol of a randomized, double-blind, placebo-controlled trial.

Anne T Leerling, Ana Navas Cañete, Frits Smit, Neveen A T Hamdy, Alina van de Burgt, Natasha M Appelman-Dijkstra, Olaf M Dekkers, Elizabeth M Winter

Abstract readClinical Trial
In one paragraph

Trial report in JBMR plus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

8 authors.

Anne T LeerlingDepartment of Internal Medicine, Division of Endocrinology, Leiden University Medical Center, Leiden, 2333 ZA, the Netherlands.ORCID https://orcid.org/0000-0002-9780-9521
Ana Navas CañeteCenter for Bone Quality, Leiden University Medical Center, Leiden, 2333 ZA, the Netherlands.
Frits SmitCenter for Bone Quality, Leiden University Medical Center, Leiden, 2333 ZA, the Netherlands.
Neveen A T HamdyDepartment of Internal Medicine, Division of Endocrinology, Leiden University Medical Center, Leiden, 2333 ZA, the Netherlands.
Alina van de BurgtDepartment of Nuclear Medicine, Alrijne Hospital, Leiderdorp, 2353 GA, the Netherlands.
Natasha M Appelman-DijkstraDepartment of Internal Medicine, Division of Endocrinology, Leiden University Medical Center, Leiden, 2333 ZA, the Netherlands.ORCID https://orcid.org/0000-0001-5035-127X
Olaf M DekkersDepartment of Internal Medicine, Division of Endocrinology, Leiden University Medical Center, Leiden, 2333 ZA, the Netherlands.
Elizabeth M WinterDepartment of Internal Medicine, Division of Endocrinology, Leiden University Medical Center, Leiden, 2333 ZA, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic nonbacterial osteitis (CNO) is a rare auto-inflammatory bone disease affecting children and adults. Adult CNO is characterized by painful bone lesions, primarily of the anterior chest wall. There is no approved therapy for adult CNO. Current off-label treatments include intravenous bisphosphonates, which have been shown to alleviate pain through decreasing bone turnover. However, no adequately powered randomized controlled trials (RCTs) have been conducted. This double-blind, placebo-controlled RCT investigates the efficacy of intravenous pamidronate to decrease bone pain in adult CNO patients. Recruiting at the Dutch national referral center for CNO, adult patients with persistent bone pain despite non-steroidal anti-inflammatory drugs, or optionally other standard-of-care treatments are randomized to receive two courses of intravenous pamidronate (at 0 and 3 mo, 30 mg daily, on 3 consecutive d) or placebo. From 6 mo onwards, all patients receive open-label pamidronate for another two courses. The primary outcome is change in score for maximum pain from 0 to 6 mo. Secondary outcomes include change in quantitative intralesional bone turnover as measured on sodium-fluoride positron emission computed tomography ([

Indexed as

[18f]naf-pet/ctbisphosphonatesclinical trialCNOCRMOimagingosteitisosteomyelitispainpamidronaterare diseasessapho

Identifiers

PMID39323655
PMCPMC11422776

What OpenQuestion holds

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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 OpenQuestion graph.