Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07044557

MeDex: No Perioperative Dexamethasone in Brain Metastases

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
35 (estimated)
Sponsor
University of Louisville · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Perioperative treatment of newly diagnosed cancer patients with brain metastasis without dexamethasone (Dex).

Detailed description

This is a single-arm trial, assessing the safety and efficacy of brain metastasis resection without perioperative Dex in a maximum of 35 patients screened and enrolled in our emergency room and clinics. Investigators will assess efficacy by noting presence of absence of lymphopenia. The patients will be followed until initiation of postoperative adjuvant cancer therapy for collection of primary and secondary endpoints.

Conditions

Interventions

TypeNameDescription
OTHERWithholding perioperative DexamethasonePatients will not receive perioperative Dex before, during, and up to 3 weeks after surgery.

Timeline

Start date
2025-12-03
Primary completion
2027-10-01
Completion
2027-10-01
First posted
2025-07-01
Last updated
2026-01-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07044557. Inclusion in this directory is not an endorsement.