Primary completion date changed from estimate of Dec 2026 to Oct 2, 2026
Enrollment target: estimated 50 to confirmed 52
Eligibility criteria expanded, about 15 words
Site details revised
MinorPrimary completion pushed from Jun 2026 to Dec 2026
Study completion pushed from Jun 2027 to Dec 2027
v23
MinorStudy sites: 2 to 1v22
MinorPrimary completion date: Dec 2025 to Jun 2026
Study completion date: Dec 2026 to Jun 2027
v21
MinorPrimary completion date: Jul 2025 to Dec 2025
Study completion date: Jul 2026 to Dec 2026
v20
Show 18 earlier versionsHide 18 earlier versions
MinorPrimary completion date: Jan 2025 to Jul 2025
Study completion date: Jan 2026 to Jul 2026
Site contacts updated at 1 of 2 sites
v19
MinorSite contacts updated at 2 of 2 sitesv18
MinorSite contacts updated at 1 of 2 sitesv17
Minor2 versionsRe-verified since Oct 5, 2023, no change to tracked fieldsv15-v16
MinorStudy sites: 1 to 2v14
NotablePrimary completion date: Jan 2023 to Jan 2025
Study completion date: Jan 2024 to Jan 2026
v13
Minor3 versionsRe-verified since Feb 23, 2022, no change to tracked fieldsv10-v12
MinorSite contact updatedv9
MinorSite contact updatedv8
NotablePrimary completion date: Jan 2022 to Jan 2023
Study completion date: Jan 2023 to Jan 2024
v7
MinorSite contact updatedv6
MinorEligibility criteria expanded, about 8 words
Site contact updated
v5
MinorStudy description revisedv4
MinorRe-verified, no change to tracked fieldsv3
NotableTrial status: Not Yet Recruiting to Recruiting
Start date: Feb 2019 to Apr 22, 2019
Site details revised
v2
MinorStudy First Submitted
Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This is a randomized control trial testing the effect of walnut supplementation on prostate cancer progression in 50 men with biopsy confirmed prostate cancer and planning to undergo RP. Patients consented to the study will be randomly assigned to either continue their usual diets (control arm) or to the walnut arm for 4-10 weeks depending on the window between their consent date and the date for RP.