Recruiting PHASE2 Low Grade Glioma

New treatment option for Low Grade Glioma

Official title Post-Operative Dosing of Dexamethasone in Patients With Brain Tumors After a Craniotomy, PODS Trial

ClinicalTrials.gov ID: NCT06132685

What this study is testing

What is Dexamethasone?

Dexamethasone is an investigational medicine, given as an infusion into a vein, being studied as a potential treatment for low grade glioma.

Also referred to as Aacidexam, Adexone.

Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.

What it's testing
This phase II trial tests the effect of decreasing (tapering) doses of dexamethasone on steroid side effects in patients after surgery to remove (craniotomy) a brain tumor. Steroids are the gold standard post-surgery treatment to reduce swelling (edema) at the surgical site to reduce neurological symptoms.
  • Phase 2: a mid-size study of how well it works
  • Which group you join is decided by chance.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 and older

You may be able to join if

  • Patients with radiographic findings consistent with either HGG, LGG, Meningioma, or brain metastasis
  • Age equal to or above 18

You likely can't join if

  • Known hypothalamic-pituitary-adrenal (HPA) axis dysfunction
  • Tumor causing compression of the sella or pituitary dysfunction
  • Known immunodeficiency - including but not limited to severe combined immunodeficiency (SCID), common variable immunodeficiency (CVID)...
  • Taking immunosuppressive drugs - including but not limited to methotrexate, mycophenolate, rapamycin, tacrolimus, adalimumab, infliximab. Greater...
  • Current lymphoma or leukemia
  • History of solid organ transplant
See the full eligibility criteria
Who can join
  • Patients with radiographic findings consistent with either HGG, LGG, Meningioma, or brain metastasis
  • Age equal to or above 18
What rules you out
  • Known hypothalamic-pituitary-adrenal (HPA) axis dysfunction
  • Tumor causing compression of the sella or pituitary dysfunction
  • Known immunodeficiency - including but not limited to severe combined immunodeficiency (SCID), common variable immunodeficiency (CVID), lymphocytopenia
  • Taking immunosuppressive drugs - including but not limited to methotrexate, mycophenolate, rapamycin, tacrolimus, adalimumab, infliximab. Greater than two weeks of recent daily corticosteroid use or the use of...
  • Current lymphoma or leukemia
  • History of solid organ transplant
  • Minors \< 18
  • Pregnant women
  • History of cerebrovascular accident leading to neurologic deficit

The study team makes the final eligibility decision.

Where it's taking place

  • Atlanta, Georgia, United States

Compensation & support

Compensation mentioned.

ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.

Questions & answers

Do participants get paid in this trial?

This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Atlanta, Georgia, United States. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.