Oxiblume:CoQ10 (Ralivia) Therapy for Chronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS)

NCT07629505 | Recruiting

• 1 other identifier: Ralivia_CPPS- 22/5/26
• Study Type: interventional
• Target: 100
• Locations: 1 country
• Sites: 1

Brief Summary

Chronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS) has a huge socioeconomic impact.Presently, a ''scientific dead-end'' regarding effective treatment of CP/CPPS is reported. Promising results of clinical studies, regardless their limitations, upon efficacy of phytotherapy for CP/CPPS patients have been published .Phytotherapy is cost effective and avoids the systemic side effects of other treatments being a therapy with the possibility of repeating the treatment protocol at any time. Certain important issues, regarding the efficacy and safety of phytotherapy, remain to be answered thus investing scientifically and economically to the concept of phytotherapy for CP/CPPS, definitively seems to be a move to the right direction. In this concept we will conduct a double-blind placebo-controlled randomized clinical trial assessing treatment efficacy and safety of Oxiblume:CoQ10 (Ralivia) therapy for CP/CPPS The study will be coordinated by the research office of 1st Urology Department, G. Gennimatas Hospital, Aristotle University of Thessaloniki, Greece. The research office will also support the project (logistics, quality control, management, data acquisition, publications). Patients visits will be carried out in the CP/CPPS Research Unit of the 1st Urology Department, G. Gennimatas Hospital, Aristotle University of Thessaloniki, Greece. Laboratory tests of all patients will be performed at the same microbiology laboratory. Study population A total of 100 patients (50 in Group A and 50 in Group B) with CP/CPPS diagnosis will participate in this study. Inclusion and exclusion criteria Inclusion criteria:

• Adverse events rate in all patients during study period.
• The difference between the Group A and Group B in the change of the pain domain of NIH-CPSI score from baseline to 6 weeks after treatment start.
• The difference between the Group A and Group B in the change of the following parameters from baseline to 6 and 12 weeks after treatment initiation
• Total NIH-CPSI score (Q1-9)
• Urinary symptoms (Q 5-6) and quality of life domains (Q 7-9) of the NIH-CPSI score
• IIEF-ED score
• IPSS
• UPPOINTS phenotype- number of positive domains
• Psa value
• TNFa, IL 6 values
• Active treatment (Ralivia) Group : 1 pill of Ralivia per os/day for a 3-month period
• Placebo Group : 1 placebo pill per os/day for a 3-month period Adverse events will be reported. FU Visit 1: 6 weeks after treatment initiation NIH-CPSI, IPSS, IIEF-ED questionnaires will be answered. Adverse events will be reported. Clinical symptoms assessed, in order to determine UPOINT status. PSA TNFa, IL 1β, IL 6, IL 10 blood test. FU Visit 2: 12 weeks after treatment initiation NIH-CPSI, IPSS, IIEF-ED questionnaires will be answered. Adverse events will be reported. Clinical symptoms assessed, in order to determine UPOINT status. DRE will be performed . PSA TNFa, IL 6 blood test

Conditions

Chronic Pelvic Pain Syndrome (CPPS)

Outcome Measures

Primary Outcomes (1)

• The difference between the Group A and Group B in the change of the pain domain of National Institutes of Health Chronic Prostatitis Symptom Index (NIH-CPSI) score from baseline to 12 weeks

  From enrollment to the end of treatment at 12 weeks

Secondary Outcomes (10)

• The difference between the Group A and Group B in the change of the pain domain of NIH-CPSI score from baseline to 6 weeks

  From baseline to 6 weeks

• The difference between the Group A and Group B in the change of Total NIH-CPSI score (Q1-9) from baseline to 6 and 12 weeks

  From baseline to 6 and 12 weeks

• The difference between the Group A and Group B in the change of Urinary symptoms (Q 5-6) and quality of life domains (Q 7-9) of the NIH-CPSI score from baseline to 6 and 12 weeks

  From baseline to 6 and 12 weeks

• The difference between the Group A and Group B in the change of International Index of Erectile Function -Erectile Domain (IIEF-ED ) score from baseline to 6 and 12 weeks

  From baseline to 6 and 12 weeks

• The difference between the Group A and Group B in the change of International Prostate Symptom Score (IPSS) from baseline to 6 and 12 weeks

  From baseline to 6 and 12 weeks

Study Arms (2)

Group A

ACTIVE COMPARATOR

Patients of the Active Group will receive 1 pill of Ralivia per os/day for a 3-month period

Dietary Supplement: Oxiblume:CoQ10 (Ralivia) therapy

Group B

PLACEBO COMPARATOR

Patients of the Placebo Group will receive 1 placebo pill per os/day for a 3-month period

Other: Placebo Pill.

Interventions

Oxiblume:CoQ10 (Ralivia) therapy DIETARY_SUPPLEMENT

1 pill of Ralivia per os/day for a 3-month period

Group A

Placebo Pill. OTHER

1 placebo pill per os/day for a 3-month period

Group B

Eligibility Criteria

• Age: 18 Years - 50 Years
• Sex: male
• Healthy Volunteers: No
• Age Groups: Adult (18-64)

You may qualify if:

• Participant must be between 18 and 50 years old.
• Participant has signed and dated the appropriate Informed Consent document.
• 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.

You may not qualify if:

• Participant has evidence of facultative Gram negative or enterococcus with a value of ≥ 1000 CFU/ml in mid-stream urine (VB2).
• Participant has a history of prostate, bladder or urethral cancer.
• Participant has undergone pelvic radiation or systemic chemotherapy.
• Participant has undergone intravesical chemotherapy.
• 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.
• Participant has undergone prostate surgery or treatment.
• Participant with penile or urinary sphincter implants.
• Participant has been diagnosed with cancer during the last 5 years or had any surgery in the pelvis.
• Participant has a neurological impairment or psychiatric disorder preventing his understanding of consent and his ability to comply with the protocol.

Sponsors & Collaborators

• G.Gennimatas General Hospital: lead

Study Sites (1)

G.Gennimatas General Hospital

Thessaloniki, 54636, Greece

RECRUITING

MeSH Terms

Interventions

Therapeutics

Central Study Contacts

IOANNIS MYKONIATIS, Professor

CONTACT

+306936975862; g_mikoniatis@hotmail.com

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Ass.Professor

Study Record Dates

• First Submitted: June 1, 2026
• First Posted: June 5, 2026
• Study Start: June 8, 2026
• Primary Completion (Estimated): December 1, 2026
• Study Completion (Estimated): December 1, 2026
• Last Updated: June 5, 2026

Record last verified: 2026-06

Data Sharing

• IPD Sharing: Will share
• Shared Documents: STUDY PROTOCOL, ICF
• Time Frame: Beginning 3 months and ending 3 years after the publication of results")

Locations

GR (1)