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NCT05500391RecruitingPhase 2

Assessment of Compliance With Monitoring Conducted by a Physician in Person or by a Nurse in Remote Monitoring

Randomized Phase II Trial Evaluating Compliance With Monitoring Conducted Either by a Hospital-based Physician in Person or by a Nurse in Remote Monitoring

Source: ClinicalTrials.gov · Last updated 18 Mar 2026

Brief summary (registry, in English)

This is a multicenter, interventional, randomized study among adult patients recently diagnosed with a rare tumor (\<12 months). The study will aim to compare compliance with the personalized post-treatment surveillance plan, established for each patient according to national guidelines, when the surveillance is conducted in person by a hospital-based physician (control arm) or remotely by a trained nurse (experimental arm).

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
88 (estimated)
First submitted
10 Aug 2022
Start date
28 Feb 2024
Primary completion date
Oct 2026
Lead sponsor
Centre Oscar Lambret
NCT number
NCT05500391

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 88
  • From 28 Feb 2024 to the primary completion date, Oct 2026
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Contraindication to imaging tests required for the surveillance plan
  • No telephone
  • Patient under guardianship or curatorship

Who the study is looking for

  • Positive diagnosis (anatomopathology) of tumor within 12 months
  • Patient 18 years of age or older
  • Patient with one of the following conditions:
    • Desmoid fibromatosis of the abdominal wall operated on or under active surveillance
    • Stage I testicular seminoma (whether or not treated with carboplatin AUC7)
    • Stage I non-seminomatous germ cell tumor (with or without adjuvant BEP chemotherapy)
    • Operated GIST with low risk of relapse
    • Rare gynecological tumors (sex cord and stromal tumors; germ cell tumors of the ovary, clear cell adenocarcinoma, mucinous adenocarcinoma of the ovary, borderline tumors, small cell carcinoma, ovarian and uterine carcinosarcoma, low grade serous tumors), operated
    • Low-grade glioma, operated
    • Low-grade neuroendocrine tumor, treated by surgery alone
  • Patient who has given consent to participate in the study

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU Amiens
Coordinator of this site? Confirm its status
AmiensFranceNot yet recruiting
Centre François Baclesse
Coordinator of this site? Confirm its status
CaenFranceNot yet recruiting
Centre Oscar Lambret
Coordinator of this site? Confirm its status
LilleFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.