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OncoMatch/Clinical Trials/NCT03739502

A Randomized Phase II Study of Hyperbaric Oxygen in Improving Engraftment in Umbilical Cord Blood Stem Cell Transplant

Is NCT03739502 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Hyperbaric oxygen for aml.

Phase 2RecruitingUniversity of RochesterNCT03739502Data as of May 2026

Treatment: Hyperbaric oxygenThe UCB transplant is a type of stem cell transplant used to treat cancer of the blood or lymph glands. The UCB transplant has advantages over other types of transplants such as ease of obtaining the umbilical cord blood, absence of donor risks, reduced risks of contagious infections, and the availability for immediate use. The UCB transplant is also associated with a lower incidence of graft versus host disease, or GvHD (in GvHD, the transplanted graft attacks the recipient organs).

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Extracted eligibility criteria

Cancer type

Acute Myeloid Leukemia

Non-Hodgkin Lymphoma

Hodgkin Lymphoma

Acute Lymphoblastic Leukemia

Myelodysplastic Syndrome

Biomarker criteria

Required: BCR BCR-ABL gene positivity

BCR-ABL gene positivity (high-risk ALL feature)

Required: ABL1 BCR-ABL gene positivity

BCR-ABL gene positivity (high-risk ALL feature)

Excluded: NPM1 mutation without FLT3-ITD

NPM1 mutation without FLT3-ITD (favorable risk, excluded from AML CR1 inclusion)

Excluded: FLT3 ITD

NPM1 mutation without FLT3-ITD (favorable risk, excluded from AML CR1 inclusion)

Excluded: CEBPA double-mutated

double-mutated CEBPA (favorable risk, excluded from AML CR1 inclusion)

Prior therapy

Must have received: high-dose therapy — relapsed

relapsed following high-dose therapy (HD) [Hodgkin's disease]; relapsed post-high-dose therapy and autologous transplantation [NHL]

Cannot have received: intrathecal chemotherapy

Exception: within 2 weeks of starting preparative regimen

Patients who had intrathecal chemotherapy within 2 weeks of starting preparative regimen

Cannot have received: cranial irradiation

Exception: within 4 weeks of starting preparative regimen

cranial irradiation within 4 weeks of starting preparative regimen

Lab requirements

Kidney function

creatinine: ≤ 1.5 x uln

Liver function

alt, ast: < 4x iuln; total bilirubin: ≤ 2.0 mg/dl

Cardiac function

ef measured by 2d-echo or muga scan of ≥ 45%; ekg with no clinically significant arrhythmia

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • University of Rochester · Rochester, New York

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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