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NCT06968910: Urol-CBD

CBD-based Therapy to Attenuate Non-bacterial Prostatitis Symptoms

Completed NA Last updated 13 May 2025
What this trial tests

NA trial testing CANNEFF® SUP rectal suppositories in Prostatitis in 35 participants. Completed in 1 January 2025.

Timeline
1 December 2022
Primary endpoint
1 April 2024
1 January 2025

Quick facts

Lead sponsorPalacky University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposesupportive care
Enrollment35
Start date1 December 2022
Primary completion1 April 2024
Estimated completion1 January 2025
Sites1 location across Czechia

Drugs / interventions tested

Conditions studied

Sponsor

Palacky University

Who can join

Adults 18 to 50, male only, with Prostatitis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Efficacy and safety of the medical device rectal CANNEFF® SUP suppositories containing two active ingredients cannabidiol (CBD) and hyaluronic acid (HA) in alleviating non-bacterial prostatitis symptoms and improving quality of life in men will be evaluated.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Exploring the therapeutic potential of cannabidiol in soft tissue wound healing: Delivery strategies and anti-inflammatory pathways.
    Dubnika A, Jurgelane I, Grava-Ceplite A, Tornaci S, et al · · 2026 · cited 1× · PMID 42039297 · DOI 10.1016/j.apsb.2025.10.001

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Other Palacky University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06968910.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing