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RecruitingInterventionalPhase 2

Post-Operative Dosing of Steroids Post Craniotomy for Brain Tumor (PODS)

NCT ID: NCT06132685Sponsor: Emory UniversityLast updated: 2026-02-10

Summary

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. Although, corticosteroids reduce edema, they have side effects including high blood sugar, high blood pressure, and can impair wound healing. Dexamethasone is in a class of medications called corticosteroids. It is used to reduce inflammation and lower the body's immune response. It also works to treat other conditions by reducing swelling and redness. Tapering doses dexamethasone may decrease steroid side effects without increasing the risk of edema in patients with brain tumors after a craniotomy.

Detailed description

PRIMARY OBJECTIVES: I. The primary objective of this study is to evaluate the efficacy of a reduced dosage steroid schedule (RDS) in patients who have undergone craniotomy for high grade glioma (HGG), low grade glioma (LGG), brain metastasis (BM), and meningiomas as compared with the normal dosing schedule (NDS). II. RDS after undergoing craniotomy for brain tumor has no impact on length of stay, 30 day readmission, and need for repeat imaging when compared to NDS. SECONDARY OBJECTIVE: I. RDS after craniotomy for brain tumor has no impact on development of steroid related side effects (new onset or worsening hypertension, hyperglycemia, wound infection, impaired wound healing, steroid dependence, neuropsychiatric disturbance) when compared to NDS. TERTIARY/EXPLORATORY OBJECTIVE: I. RDS after craniotomy has no effect on lymphocyte count and differential at 10-14 days after surgery. OUTLINE: Patients are randomized to 1 of 2 arms. ARM I (NDS): Patients receive tapering doses of dexamethasone on days 1-15. Patients also undergo blood sample collection at time of surgery, at follow up visits and optionally at wound check visit 10-14 days post operative at investigator availability. Patients additionally undergo magnetic resonance imaging (MRI) and computed tomography (CT) scan during inpatient stay as part of standard of care. ARM II (RDS): Patients receive tapering doses of dexamethasone on days 1-4. Patients may receive dexamethasone intravenously (IV) and restart the taper if clinically indicated. Patients also undergo blood sample collection at time of surgery, follow up visits and optionally at wound check visit 10-14 days post operative at investigator availability. Patients additionally undergo MRI and CT scan during inpatient stay as part of standard of care.

Arms & interventions

  • ProcedureBiospecimen Collection

    Undergo blood sample collection

  • ProcedureComputed Tomography

    Undergo CT scan

  • DrugDexamethasone

    Given dexamethasone or IV

  • ProcedureMagnetic Resonance Imaging

    Undergo MRI

  • OtherQuestionnaire Administration

    Ancillary studies

Outcome measures

Primary

  • Length of hospital stay

    The two-sample t-test or Mann-Whitney U test utilized to estimate the differences between the two groups. General linear model employed in the multivariable analysis to estimate the adjusted difference in length of hospital stay between the two groups after adjusting for other factors.

    Time frame: Up to 3 months

  • 30-day repeat admission rate

    Comparison between the two groups assessed using Fisher exact test or Chi-Square test. Logistic regression used to compare between the two groups after adjusting for other factors. Odds ratios (OR) and 95% confidence intervals (CIs) calculated to evaluate the strength of any association.

    Time frame: At 30 days after surgery

  • Need for repeat head imaging

    Comparison between the two groups assessed using Fisher exact test or Chi-Square test. Logistic regression used to compare between the two groups after adjusting for other factors. OR and 95% CIs calculated to evaluate the strength of any association.

    Time frame: Up to 3 months

Secondary

  • Incidence of new neurologic deficit

    Time frame: At less than 30 days and at 3 months

  • Breakthrough seizures

    Time frame: Up to 30 days after surgery

  • Evidence of Worsening Cerebral Edema

    Time frame: Between 5 and 30 days after surgery

  • Evaluation for Steroid Dependence

    Time frame: At long term follow up to 3 months after surgery

  • Rate of new onset hypertension

    Time frame: During inpatient stay up to 3 months after surgery

  • Rate of new onset hyperglycemia

    Time frame: During inpatient stay up to 3 months after surgery

  • Evaluation for Wound infection or Delayed Wound Healing

    Time frame: At 2 week wound check after surgery

  • Evaluation for Need for Psychiatric Consult or Neuropsychiatric Side Effects

    Time frame: At 2 week follow up after surgery

  • Change in lymphocyte count and differential

    Time frame: At baseline and 10-14 days post-operative

Eligibility criteria

Sex: AllAge: 18 Years and olderHealthy volunteers: No
Inclusion Criteria: * Patients with radiographic findings consistent with either HGG, LGG, Meningioma, or brain metastasis * Age equal to or above 18 Exclusion Criteria: * 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 corticosteroids equivalent to \> 85 mg of dexamethasone in the last month * Current lymphoma or leukemia * History of solid organ transplant * Minors \< 18 * Pregnant women * History of cerebrovascular accident leading to neurologic deficit

Study locations (1)

Emory University Hospital/Winship Cancer Institute

Atlanta, Georgia, 30322

Recruiting
Agnes Harutyunyan · Contact
Kimberly Hoang, MD · Principal Investigator