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Feasibility analysis of nasoduodenal feces administration to eradicate resistant enterobacteriaeceae.

Feasibility analysis of nasoduodenal feces administration to eradicate resistant enterobacteriaeceae. - FANFARE

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON38475
Enrollment
10
Registered
2014-03-21
Start date
2014-06-30
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

nierfalen waarvoor niertransplantatie ESBL urinary tract infections and ESBL colonisation

Interventions

Donor feces infusion.

Sponsors

Academisch medisch centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Renal transplant recipients colonised by ESBL producing Entrobacteriaceae in the large intestine. Stable renal allograft function with maintenance dose of immunosuppressive therapy. No food allergies.

Exclusion criteria

Exclusion criteria: 1: Patients with ESBL strain in urine which is resistant to first line antibiotics (as nitrofurantoin) 2: Patients still being ESBL positive in throat or urine despite pre-treatment with chlorhexidin or first line antibiotic (as nitrofurantoin). 3: Experiencing rejection episode which require high dose immune-suppressants or critically ill recipients admitted to the ICU. 4: Signs of diminished bowel passage or ileus 5: Recent endoscopy with biopsies within last three months 6: Pregnancy 7: Known food allergie to any kind of food products. 8: Heavily immunocompromised patients ( prednisone use of > 60 mg per day or CD4 count

Design outcomes

Primary

MeasureTime frame
Primary outcome is ESBL decolonisation of the rectum after 12 weeks post donor feces infusion.

Secondary

MeasureTime frame
1: Development of ESBL related urinary tract infection within 24 weeks follow-up time after donor feces infusion. 2: Changes in microbiome prior and after donor feces infusion.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)