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CompletedNCT03620305Updated Feb 18, 2019

Septic Pseudarthrosis Of Long Bone : Experience In A Regional Reference Center

An observational study in Pseudoarthrosis of Bone, sponsored by Hospices Civils de Lyon. Completed at 1 site in France. Open to participants aged 18 Years to 100 Years. Per ClinicalTrials.gov, last updated 2019-02-18.

Sponsored by Hospices Civils de Lyon · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
20
Ages
18 Years to 100 Years
Sex
All
01

Study summary

Description of septic pseudarthrosis with chirurgical treatment in two steps (first step : Implementation of cement, second step : bone reconstruction, with or without device)

02

Conditions studied

  • Pseudoarthrosis of Bone

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03

In context

Pseudarthrosis

41 studies on the registry are indexed under Pseudarthrosis; 7 are open to participants now.

This study's enrollment of 20 is below the median of 60 across 16 observational studies indexed under Pseudarthrosis.

Browse Pseudarthrosis studies →

Lead sponsor

Hospices Civils de Lyon is the lead sponsor of 1,866 studies on the registry; 448 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 100 Years
Sexes eligible
All
Sampling method
Non-probability sample

Study population

: patients having septic pseudarthrosis managed with 2 steps chirurgical treatment

Inclusion criteria

  • patients having septic pseudarthrosis of long bone treated at the CRIOAc LYON

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
20 participants (actual)
Patient registry
No

Groups and cohorts

  • Description of treatment of septic pseudarthrosis

    chirurgical and medical treatment

    Other: Description of treatment of septic pseudarthrosis

Interventions

  • OtherDescription of treatment of septic pseudarthrosis

    description of chirurgical 2 steps management of septic pseudarthrosis

06

What researchers measure

Primary outcomes

  1. Description of treatment of septic pseudarthrosis : chirurgical treatment - rate of use of this type of chirurgical treatment among patients with septic pseudarthrosis

    Description of treatment of septic pseudarthrosis : chirurgical treatment

    Time frame: Outcome is measured at the end of follow-up (usually between 12 and 24 months after antibiotic therapy disruption)

Secondary outcomes

  1. Description of treatment of septic pseudarthrosis : medical treatment - duration of treatment in patients having sepstic pseudarthrosis

    Description of treatment of septic pseudarthrosis : medical treatment

    Time frame: Outcome is measured at the end of follow-up (usually between 12 and 24 months after antibiotic therapy disruption)

  2. Treatment failure : rate of failure with this 2 times chirurgical treatment

    Treatment failure is defined by local clinical and/or microbiological relapse; and/or need for additional surgery; death of septic origin

    Time frame: Outcome is measured at the end of follow-up (usually between 12 and 24 months after antibiotic therapy disruption)

07

Study locations

1 site
  • Hospices Civils de Lyon
    Lyon, 69004, France
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 18, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03620305
Responsible party
Eugénie MABRUT (CRA, Hospices Civils de Lyon) — Principal investigator
First posted
Aug 8, 2018
Start date
Apr 1, 2018
Primary completion
Dec 30, 2018
Completion
Dec 30, 2018
Last update
Feb 18, 2019

Study contacts

Tristan Ferry
principal investigator · Hospices Civils de Lyon - Hôpital Croix-Rousse

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2019. You cannot join it, but the record below documents what was studied.

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