National Clinical-biological Prospective Cohort of Incident Cases of Aggressive Fibromatosis (ALTITUDES)

NCT02867033 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 628

Last updated 2026-03-30

No results posted yet for this study

Summary

The purpose of this study is to constitute the French largest Aggressive fibromatosis cohort.

Conditions

  • Aggressive Fibromatosis

Interventions

PROCEDURE

biopsy

pre-therapeutic or post-therapeutic biopsy or resected tissues

OTHER

biobank constitution

Constitution of a biobank with pre-therapeutic or post-therapeutic biopsy or resected tissues

PROCEDURE

Coloscopy

For adult patients, a coloscopy with chromoscopy of ascending and sigmoid colon will be performed

PROCEDURE

Blood sampling (facultative)

Blood sample can be collected at diagnostic or after medically significant events (progressive disease, local or systemic treatment, pregnancy...)

OTHER

Pain evaluation

Pain evaluation (EVA scale), anxiety (HADS questionnaire), quality of life questionnaire (EORTC-QLQ-C30)

PROCEDURE

Tumor biobank realization

Realization of a tumor biobank is part of classical procedure of participating centers

Sponsors & Collaborators

  • Ligue contre le cancer, France

    collaborator OTHER
  • Institut Curie

    collaborator OTHER
  • Hôpital de la Timone

    collaborator OTHER
  • SOS Desmoid e.V.

    collaborator UNKNOWN
  • APICIL funding

    collaborator UNKNOWN
  • GIRCI NO

    collaborator UNKNOWN
  • UNICANCER

    collaborator OTHER
  • Groupement Interrégional de Recherche Clinique et d'Innovation

    collaborator OTHER
  • Centre Oscar Lambret

    lead OTHER

Principal Investigators

  • Nicolas PENEL, PhD · Centre Oscar Lambret

  • Sébastien SALAS, PhD · Hopital Timone adultes

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-03-22
Primary Completion
2030-11-30
Completion
2030-11-30

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02867033 on ClinicalTrials.gov