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The SUPRAMAX Study: Supramaximal Resection Versus Maximal Resection for High-Grade Glioma Patients (ENCRAM 2201)

Launched by JASPER GERRITSEN · Nov 1, 2023

Trial Information

Current as of July 23, 2025

Recruiting

Keywords

Glioblastoma Supramaximal Resection Flai Rectomy Non Contrast Enhancement Neurological Morbidity Quality Of Life Overall Survival Progression Free Survival

ClinConnect Summary

The SUPRAMAX Study is researching the effects of two different surgical approaches for treating patients with high-grade gliomas, which are aggressive types of brain tumors. Specifically, the study compares "supramaximal resection" (SMR), which involves removing more of the tumor, including parts that are not clearly visible on scans, versus "maximal resection," which focuses only on the visible tumor. The goal is to see if removing more of the tumor can lead to better survival rates and improved quality of life for patients. The study will also look at how well patients recover after surgery and which patients may benefit the most from this approach.

To participate in the trial, patients need to be between 18 and 90 years old and have a confirmed diagnosis of high-grade glioma. They must also be able to provide informed consent. The study is currently recruiting participants and is being conducted at various medical centers across Europe and North America. Patients who join the study can expect to undergo surgery and will be monitored over several months to track their recovery and overall health. It's important for patients to know that this research aims to improve treatment options for future patients with similar conditions.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Age ≥18 years and ≤90 years
  • 2. Tumor diagnosed as HGG (WHO grade III/IV) on MRI as assessed by the neurosurgeon
  • 3. Written informed consent
  • Exclusion Criteria:
  • 1. Tumors of the cerebellum, brainstem or midline
  • 2. Multifocal contrast enhancing lesions
  • 3. Medical reasons precluding MRI (e.g. pacemaker)
  • 4. Inability to give written informed consent
  • 5. Secondary high-grade glioma due to malignant transformation from low-grade glioma
  • 6. 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

About Jasper Gerritsen

Jasper Gerritsen is a dedicated clinical trial sponsor committed to advancing medical research through innovative and ethical study design. With a focus on enhancing patient outcomes, Jasper Gerritsen collaborates with leading healthcare professionals and institutions to conduct rigorous clinical trials across various therapeutic areas. The organization prioritizes transparency, compliance, and the highest standards of scientific integrity, ensuring that all trials are conducted with the utmost care for participant safety and data quality. By leveraging cutting-edge methodologies and fostering strong partnerships, Jasper Gerritsen aims to contribute significantly to the development of new therapies that address unmet medical needs.

Locations

Boston, Massachusetts, United States

Heidelberg, , Germany

Leuven, , Belgium

Heidelberg, Baden Württemberg, Germany

San Francisco, California, United States

Bern, , Switzerland

Rotterdam, Zuid Holland, Netherlands

Munich, Bavaria, Germany

The Hague, Zuid Holland, Netherlands

Patients applied

0 patients applied

Trial Officials

Jasper Gerritsen, MD PhD

Principal Investigator

Erasmus Medical Center

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported