Fact CheckerSign in

NCT06146725Recruiting

The RESBIOP-study: Resection Versus Biopsy in High-grade Glioma Patients (ENCRAM 2202)

Source: ClinicalTrials.gov · Last updated 27 Nov 2023 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

There are no guidelines or prospective studies defining the optimal surgical treatment for gliomas of older patients (≥70 years) or those with limited functioning performance at presentation (KPS ≤70). Therefore, the decision between resection and biopsy is varied, amongst neurosurgeons internationally and at times even within an instiutition. This study aims to compare the effects of maximal tumor resection versus tissue biopsy on survival, functional, neurological, and quality of life outcomes in these patient subgroups. Furthermore, it evaluates which modality would maximize the potential to undergo adjuvant treatment. This study is an international, multicenter, prospective, 2-arm cohort study of observational nature. Consecutive HGG patients will be treated with resection or biopsy at a 3:1 ratio. Primary endpoints are: 1) overall survival (OS) and 2) proportion of patients that have received adjuvant treatment with chemotherapy and radiotherapy. Secondary endpoints are 1) proportion of patients with NIHSS (National Institute of Health Stroke Scale) deterioration at 6 weeks, 3 months and 6 months after surgery 2) progression-free survival (PFS); 3) quality of life at 6 weeks, 3 months and 6 months after surgery and 4) frequency and severity of Serious Adverse Events (SAEs). Total duration of the study is 5 years. Patient inclusion is 4 years, follow-up is 1 year.

Status (registry)
Recruiting
Study type
Observational
Enrollment
564 (estimated)
First submitted
18 Nov 2023
Start date
1 Jan 2023
Primary completion date
1 Jan 2028
Lead sponsor
Jasper Gerritsen
Diseases
Glioblastoma
NCT number
NCT06146725

What you commit to

  • Study type: Observational
  • Planned participants: 564
  • From 1 Jan 2023 to the primary completion date, 1 Jan 2028
  • 8 sites in 5 countries
  • 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 illness

  • Secondary high-grade glioma due to malignant transformation from low-grade glioma
  • Second primary malignancy within the past 5 years with the exception of adequately treated in situ carcinoma of any organ or basal cell carcinoma of the skin

Other

  • Tumors of the cerebellum, brainstem or midline
  • Medical reasons precluding MRI (e.g. pacemaker)
  • Inability to give written informed consent

Who the study is looking for

  • Age ≥18 years and ≤90 years
  • Tumor diagnosed as HGG (WHO grade III/IV) on MRI as assessed by the neurosurgeon
  • Written informed consent

Age in the registry: 18 years to 90 years · Sex: All

Full criteria on ClinicalTrials.gov

Sites (8)

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

SiteCityCountrySite status
University Hospital Leuven
Coordinator of this site? Confirm its status
LeuvenBelgiumRecruiting
Inselspital Universitätsspital Bern
Coordinator of this site? Confirm its status
BernSwitzerlandNot yet recruiting
University Hospital Heidelberg
Coordinator of this site? Confirm its status
HeidelbergGermanyRecruiting
Technical University Munich
Coordinator of this site? Confirm its status
MunichGermanyNot yet recruiting
Erasmus Medical Center
Coordinator of this site? Confirm its status
RotterdamNetherlandsRecruiting
Haaglanden Medical Center
Coordinator of this site? Confirm its status
The HagueNetherlandsRecruiting
Massachusetts General Hospital
Coordinator of this site? Confirm its status
BostonUnited StatesRecruiting
University of California San Francisco
Coordinator of this site? Confirm its status
San FranciscoUnited StatesRecruiting

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