Skip to content

Fecal microbiota transplantation for primary sclerosing cholangitis - randomized study versus sham transplantation (FMT-SCLER).

Status
Not yet recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-505469-95-00
Acronym
APHP211053
Enrollment
72
Registered
2025-12-02
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-02

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

Conditions

Primary Sclerosing Cholangitis

Brief summary

Proportion of success at week 48. Success is defined as patients with serum ALP <1.3 ULN at week 48 and a reduction of, at least 15%, compared to baseline ALP level AND total bilirubin ≤ 1 ULN at week 48

Detailed description

Proportion of patients with serum ALP <1.3 ULN and a reduction of at least 15% compared to baseline ALP level at week 12 24 36 and 48, Proportion of patients that normalized total bilirubin at week 12 ,24 36 and 48 (total bilirubin <1 ULN), Proportion of patients that normalized ALP at week 12 24 36 and 48 (ALP <1 ULN), Proportion of patients that normalized all liver tests (ALP <1ULN and GGT <1 ULN and AST <1 ULN and ALT <1 ULN and total bilirubin <1 ULN) at week 12 24 36 and 48, Change in Elastometry between week 0 and week 48, PSC Prognostic scores including the MELD score, the Revised PSC Mayo Risk Score, the Amsterdam-Oxford prognostic model (week 0, week 24, week 48), Safety endpoints: - Percentage of patients with clinical (including infectious events and increased IBD activity) or biological adverse events (leucocytes, CRP) during the study period (overall and between randomization and week 48, between randomization and week 104) - Survival rate without liver events (decompensation of cirrhosis, acute cholangitis, jaundice, need for ERCP) at week 48, Pruritus (VAS and 5D pruritus scale) at week 0, 12, 24, 36 and 48, Symptoms and quality of life (PRO-CSP questionnaire, QMCF questionnaire – Questionnaire de la maladie chronique du foie) and fatigue (PBC 40 questionnaire) : at week 0, week 24 and week 48, Bile acids measured by chromatography at week 0, week 48, Cholangiographic abnormalities, assessed by magnetic resonance cholangiography at week 0, week 48, Changes in IBD activity: clinical score between week 0 and week 48 (HBI and Crohn’s disease Activity Index [CDAI] for Crohn’s disease and Mayo score for Ulcerative colitis), fecal calprotectin and endoscopic score assessed by colonoscopy (Crohn’s disease Endoscopic Index of Severity [CDEIS] for Crohn’s disease and ulcerative colitis Endoscopic Index of Severity [UCEIS] for ulcerative colitis)., Analysis of gut microbiota at week 0, 12, 24, 36 and 48.

Interventions

Sponsors

Assistance Publique Hopitaux De Paris
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Proportion of success at week 48. Success is defined as patients with serum ALP <1.3 ULN at week 48 and a reduction of, at least 15%, compared to baseline ALP level AND total bilirubin ≤ 1 ULN at week 48

Secondary

MeasureTime frame
Proportion of patients with serum ALP <1.3 ULN and a reduction of at least 15% compared to baseline ALP level at week 12 24 36 and 48, Proportion of patients that normalized total bilirubin at week 12 ,24 36 and 48 (total bilirubin <1 ULN), Proportion of patients that normalized ALP at week 12 24 36 and 48 (ALP <1 ULN), Proportion of patients that normalized all liver tests (ALP <1ULN and GGT <1 ULN and AST <1 ULN and ALT <1 ULN and total bilirubin <1 ULN) at week 12 24 36 and 48, Change in Elastometry between week 0 and week 48, PSC Prognostic scores including the MELD score, the Revised PSC Mayo Risk Score, the Amsterdam-Oxford prognostic model (week 0, week 24, week 48), Safety endpoints: - Percentage of patients with clinical (including infectious events and increased IBD activity) or biological adverse events (leucocytes, CRP) during the study period (overall and between randomization and week 48, between randomization and week 104) - Survival rate without liver events (decompen

Countries

France

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026