Prostate Carcinoma Clinical Trial
Official title:
Evaluation of MRI With Dixon Based Sequences in the Detection of Prostate Cancer
Verified date | May 2024 |
Source | M.D. Anderson Cancer Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This trial studies the use of magnetic resonance imaging (MRI) with Dixon based imaging sequences in detecting prostate cancer. MRI uses radio waves and a powerful magnet linked to a computer to create detailed pictures of areas inside the body. Researchers hope to learn if using a modified MRI scan technique with Dixon based imaging sequencing will help to produce better images of prostate cancer than the standard of care MRI scan technique.
Status | Active, not recruiting |
Enrollment | 65 |
Est. completion date | February 2, 2027 |
Est. primary completion date | February 2, 2027 |
Accepts healthy volunteers | No |
Gender | Male |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Biopsy proven prostate cancer patients who are scheduled to undergo prostatectomy. - Patient who is scheduled to have a clinically indicated staging endorectal prostate MRI exam. - Patients who have signed their informed consent form to undergo the study. Exclusion Criteria: - Known prior hormone ablation or radiation therapy (pelvic or prostate). - Patients who do not want to undergo prostatectomy and prefer other therapy or surveillance. - Contraindication to conventional MR imaging (e. g. metal implants, pace maker, etc.). |
Country | Name | City | State |
---|---|---|---|
United States | M D Anderson Cancer Center | Houston | Texas |
Lead Sponsor | Collaborator |
---|---|
M.D. Anderson Cancer Center | National Cancer Institute (NCI) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Detection of at least one or more prostate lesions with Dixon sequencing | Will evaluate and compare the accuracy of Dixon based sequencing to the conventional T2 weighted sequencing for detection of intraprostatic tumor and extraprostatic tumor extension. Lesions will be within any of six regions of the prostate: left apex, left mid, left base, right apex, right mid, and right base. The relative sensitivity and specificity of the two sequencing methods will be compared using an adjusted McNemar's test for clustered data where clusters consist of the matched pairs of within patient-zone observations. The primary analysis will also provide 95% confidence intervals for marginal sensitivity and specificity using a generalized linear mixed model. | through study completion, an average of 1 year |
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