← Back to Clinical Trials
Recruiting NCT05911230

NCT05911230 Advanced Diffusion MRI to Differentiate Tumor Recurrence From Pseudoprogression in Patients With Glioblastoma and Brain Metastases

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT05911230
Status Recruiting
Phase
Sponsor University Hospital, Basel, Switzerland
Condition Glioblastoma (GBM)
Study Type INTERVENTIONAL
Enrollment 10 participants
Start Date 2022-11-24
Primary Completion 2025-11

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Advanced diffusion-weighted MRI (ADW-MRI)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 10 participants in total. It began in 2022-11-24 with a primary completion date of 2025-11.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This pilot study investigates whether advanced diffusion-weighted MRI (ADW-MRI) can differentiate between true tumor progression (TP) and a pseudoprogression (PsP) in patients with glioblastoma (GBM) or brain metastases.

Eligibility Criteria

Inclusion Criteria: * Patients with histopathologically proven glioblastoma or brain metastasis and suspected tumor progress on standard MRI after first line therapy and who are candidates for elective surgical resection. * Able to give informed consent Exclusion Criteria: * Contraindications to MRI (e.g. claustrophobia, pacemaker or other implants without MRI-approval, pregnancy) * Patients in a life-threatening condition * Patients in need of emergent surgery * Histopathological analyses of insufficient quality * Unable to give informed consent * Age \<18 Years

Contact & Investigator

Central Contact

Dominik Cordier, PD Dr. med.

✉ dominik.cordier@usb.ch

📞 +41 61 26 56 42

Principal Investigator

Dominik Cordier, PD Dr. med.

PRINCIPAL INVESTIGATOR

University Hospital, Basel, Switzerland

Frequently Asked Questions

Who can join the NCT05911230 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Glioblastoma (GBM). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05911230 currently recruiting?

Yes, NCT05911230 is actively recruiting participants. Contact the research team at dominik.cordier@usb.ch for enrollment information.

Where is the NCT05911230 trial being conducted?

This trial is being conducted at Basel, Switzerland.

Who is sponsoring the NCT05911230 clinical trial?

NCT05911230 is sponsored by University Hospital, Basel, Switzerland. The principal investigator is Dominik Cordier, PD Dr. med. at University Hospital, Basel, Switzerland. The trial plans to enroll 10 participants.

Related Trials

Related Intelligence Guides

In-depth guides covering this condition's trials, eligibility, and what to expect.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology