ClinicalTrials.gg
Not yet recruitingNCT06432777CABARETUpdated May 29, 2024

Recurrent Campylobacter Bacteraemia in Immunocompromised Patients

An observational study in Campylobacter Infections, sponsored by Hospices Civils de Lyon. Not yet recruiting at 1 site in France. Open to participants aged Up to 100 Years. Per ClinicalTrials.gov, last updated 2024-05-29.

Sponsored by Hospices Civils de Lyon · Observational

From the registry’s dates

  • Primary completion was expected by May 2025, 1 year 6 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
30
Ages
Up to 100 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 23 studies in Primary Immunodeficiency Diseases with a site in France — 4 open to participants now, 4 under way, none of them phase 3. Primary Immunodeficiency Diseases · France.

Planned enrollment
11th of 14
30 · median 95
Started
2024
the only one that year
Observational
14 of 23
4 open now
Registered
22nd of 23
by date

Among the 23 studies in Primary Immunodeficiency Diseases with a site in France, this one is the 11th largest by planned enrollment of the 14 observational ones that give a count, is the only one that started in 2024, is one of 14 observational ones, and was the 22nd registered.

Primary Immunodeficiency Diseases

211 studies on the registry are indexed under Primary Immunodeficiency Diseases; 51 are open to participants now.

This study's planned enrollment of 30 is below the median of 137 across 77 observational studies indexed under Primary Immunodeficiency Diseases.

Browse Primary Immunodeficiency Diseases studies →

Open to participants now

4 of the 23 studies in Primary Immunodeficiency Diseases with a site in France are open now.

All 4 open studies →

A study can be open while its sites in France have not opened yet or have stopped. Only those recruiting at a site in France →

Who these studies take

Of the 35 Primary Immunodeficiency Diseases studies recruiting now, 12 (34%) set no upper age limit and 10 (29%) stop at 75 or younger; 28 take children under 18; 11 take healthy volunteers.

This study: Up to 100 Years · all sexes · no healthy volunteers.

The full table on the hub →
Was this useful?
Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 23 studies in Primary Immunodeficiency Diseases with a site in France, or all of them as a file.
02

Study summary

Some rare cases of recurrent Campylobacter bacteraemia (RCB) exist with relapses months to years after an effective treatment and a negativation of all bacterial samples.

As of today, only around 20 cases have been described in the international literature for the last 30 years. The cases are likely highly underreported.

No study describes those recurrent Campylobacter bacteraemias at the scale of a country.

The aim of this multicentre, nationwide, retrospective study is to describe their precise epidemiology in France for the last 25 years, the immune profile of the patients, the specificities of the bacteria involved, the treatments received and the evolution of these infections.

The perspective is to propose a standardization of the medical care of those patients mainly by describing the effective treatments and the explorations of the immune system which should be considered.

03

Conditions studied

  • Campylobacter Infections

Keywords

  • primary immunodeficiency
  • Campylobacter
  • Relapsing bacteraemia
04

Who can participate

Ages eligible
Up to 100 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

French hospitals

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 2 episodes or more of Campylobacter bacteraemia separated by at least 60 days
  • AND immunodeficiency condition
  • followed by a French hospital

Exclusion criteria

Exclusion Criteria:

-Opposition of the patient

05

Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
30 participants (estimated)
Patient registry
No

Groups and cohorts

  • Recurrent Campylobacter bacteraemia

    Patients presenting at least two distinct episodes of Campylobacter bacteraemia separated by minimum 60 days and an immunodeficiency (innate or acquired) and followed by a French hospital

    Other: Characteristics of patients and Campylobacter bacteraemia episodes

Interventions

  • OtherCharacteristics of patients and Campylobacter bacteraemia episodes

    Variables: characteristics of the patients (demographic characteristics; characteristics of immunodeficiency: diagnosis, immunoglobulin dosage, white cells count etc.; chronic inflammatory bowel disease \[IBD\]), the bacteria (species, antimicrobial susceptibility) and the infection (clinical presentation, evolution, treatment received)

06

What researchers measure

Primary outcomes

  1. Description of the characteristics of the patients presenting with recurrent Campylobacter bacteraemia

    -demographic characteristics

    Time frame: Baseline

  2. Description of the characteristics of the patients presenting with recurrent Campylobacter bacteraemia

    -characteristics of immunodeficiency: diagnosis, immunoglobulin dosage, white cells count, polyvalent Ig replacement therapy

    Time frame: Baseline

  3. Description of the characteristics of the patients presenting with recurrent Campylobacter bacteraemia

    -chronic inflammatory bowel disease \[IBD\]

    Time frame: Baseline

  4. Description of the characteristics of the patients presenting with recurrent Campylobacter bacteraemia

    -characteristics of bacteraemia: clinical presentation, bacteria (species, antimicrobial susceptibility), secondary localizations, evolution, treatment modalities (antibiotics and immunother

    Time frame: Baseline

07

Study locations

1 site
  • Infectious diseases department, Hospital de la Croix Rousse,
    Lyon, 69004, France
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Jun 2024; primary completion for May 2025, 11 months later.

How these figures are worked out, and which studies are left out of them.

Registered
May 14, 2024
First posted
May 29, 2024
StartEst.
Jun 1, 2024
Primary completionEst.
May 1, 2025
CompletionEst.
May 1, 2026
Last update
May 29, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 29, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06432777
Responsible party
Sponsor
First posted
May 29, 2024
Start date
Jun 1, 2024 (estimated)
Primary completion
May 1, 2025 (estimated)
Completion
May 1, 2026 (estimated)
Last update
May 29, 2024

Study contacts

Anne CONRAD, Dr
Contact
Anne.conrad@chu-lyon.fr
+33 (0)4 72 07 11 07
Nicolas BENECH, Dr
Contact
Nicolas.benech@chu-lyon.fr

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 not yet recruiting, as verified in May 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion