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NCT05979064Recruiting

Omental Tissue Autograft in Human Recurrent Glioblastoma Multiforme (rGBM)

Laparoscopically Harvested Omental Tissue Autograft to Bypass the Blood Brain Barrier (BBB) in Human Recurrent Glioblastoma Multiforme (rGBM)

Source: ClinicalTrials.gov · Last updated 1 Jun 2026

Brief summary (registry, in English)

This single center, single arm, open-label, phase I study will assess the safety of laparoscopically harvested autologous omentum, implanted into the resection cavity of recurrent glioblastoma multiforme (GBM) patients.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
10 (estimated)
First submitted
31 Jul 2023
Start date
4 Apr 2023
Primary completion date
30 Apr 2027
Lead sponsor
Northwell Health
Diseases
Glioblastoma
NCT number
NCT05979064

What you commit to

  • Study type: Interventional
  • Planned participants: 10
  • From 4 Apr 2023 to the primary completion date, 30 Apr 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Subject intends to undergo treatment with the Gliadel® wafer at the time of this surgery.
  • Subject has had prior abdominal surgery that in the opinion of the general surgeon makes removal of omentum more risky or inadequate.

Other illness

  • Subject has an active infection requiring treatment.
  • Subject has radiographic evidence of multi-focal disease or leptomeningeal dissemination.
  • Subject has a history of other malignancy, unless the patient has been disease- free for at least 5 years. Adequately treated basal cell carcinoma or squamous cell skin cancer is acceptable regardless of time, as well as localized prostate carcinoma or cervical carcinoma in situ after curative treatment
  • Subject has a known positive test for human immunodeficiency virus infection, or active hepatitis B or hepatitis C infection.
  • Subject has a history or evidence of any other clinically significant disorder, condition or disease that would pose a risk to subject safety or interfere with the study evaluation, procedures or completion.
  • Subject has severe renal insufficiency rendering gadolinium MRI contraindicated.

Other

  • Subject, if female, is pregnant or is breast feeding.
  • Subject intends to participate in another clinical trial.
  • Subject who are unable to have an MRI scan for any reason.

Who the study is looking for

  • Subject is a male or female 18 years of age or older.
  • Subject is undergoing planned resection of known or suspected GBM.
  • Subject has a Karnofsky Performance Status (KPS) 70% or greater.
  • Subject has a life expectancy of at least 6 months, in the opinion of the Investigator.
  • Based on the pre-operative evaluation by neurosurgeon, the subject is a candidate for ≥ 80% resection of enhancing region.
  • Subject must be able to undergo MRI evaluation.
  • Subject meets the following laboratory criteria:
    • White blood count ≥ 3,000/μL
    • Absolute neutrophil count ≥ 1,500/μL
    • Platelets ≥ 100,000/μL
    • Hemoglobin \> 10.0 g/dL (transfusion and/or ESA allowed)
    • Total bilirubin and alkaline phosphatase ≤ 2x institutional upper limit of normal (ULN)
    • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) \< 3 x ULN
    • Blood urea nitrogen (BUN) and creatinine \< 1.5 x ULN
  • Females of reproductive potential must have a negative serum pregnancy test and be willing to use an acceptable method of birth control.
  • Able to understand and willing to sign an institutional review board (IRB)- approved written informed consent document
  • Subject has a histologically confirmed (frozen section) diagnosis of recurrent WHO Grade IV glioblastoma multiforme (GBM).
  • Omental graft is technically feasible.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Lenox Hill Brain Tumor Center
Coordinator of this site? Confirm its status
New YorkUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.