Oxiblume:CoQ10 Therapy for Chronic Prostatitis and Pelvic Pain

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This trial tests the efficacy and safety of Oxiblume:CoQ10 (Ralivia) versus placebo in adults with CP/CPPS. It is a randomized, double-blind, placebo-controlled design to minimize bias and assess symptom relief and tolerability. Participants must have at least three months of pelvic or perineal pain within the past six months and meet specific health criteria. The study is coordinated by the Research Office of the 1st Urology Department at G. Gennimatas General Hospital in Thessaloniki. Outcome measures and detailed methods are not fully provided here, but the design follows standard phytotherapy approaches with emphasis on safety and repeatability of treatment cycles.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Participant must be between 18 and 50 years old.
2. Participant has signed and dated the appropriate Informed Consent document.
3. Participant has had a clinical diagnosis of CP/CPPS defined as symptoms of discomfort or pain in the perineal or pelvic region for at least a three (3) month period within the last six (6) months.

Exclusion Criteria:

1. Participant has evidence of facultative Gram negative or enterococcus with a value of ≥ 1000 CFU/ml in mid-stream urine (VB2).
2. Participant has a history of prostate, bladder or urethral cancer.
3. Participant has undergone pelvic radiation or systemic chemotherapy.
4. Participant has undergone intravesical chemotherapy.
5. Participant has unilateral orchialgia without pelvic symptoms, active urethral stricture or bladder stones, or any other urological condition associated with LUTS, any neurological disease or disorder affecting the bladder.
6. Participant has undergone prostate surgery or treatment.
7. Participant with penile or urinary sphincter implants.
8. Participant has been diagnosed with cancer during the last 5 years or had any surgery in the pelvis.
9. Participant has a neurological impairment or psychiatric disorder preventing his understanding of consent and his ability to comply with the protocol.

Where it's running

• G.Gennimatas General Hospital
  Thessaloniki, Greece Recruiting

Study contacts

• Study coordinator: IOANNIS MYKONIATIS, Professor
• Email: g_mikoniatis@hotmail.com
• Phone: +306936975862

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.