A Study to Assess the Effect of Fucoidan on Prostate Health in Males With Benign Prostatic Hyperplasia

Last updated: June 3, 2025
Sponsor: Vedic Lifesciences Pvt. Ltd.
Overall Status: Completed

Phase

N/A

Condition

Prostate Disorders

Bladder Disorders

Treatment

Placebo

Fucoidan extracted from Undaria pinnatifida (UPF)

Clinical Study ID

NCT06487871
MN/231202/IP/BPH
  • Ages 45-80
  • Male

Study Summary

The present study is a randomized, double-blind, placebo-controlled study. Approximately 125 individuals will be screened, and considering a screening failure rate of 20%, at least 100 will be randomized in a ratio of 1:1 to receive either IP or placebo and will be assigned a unique randomization code. Each group will have not less than 40 completed participants after accounting for a dropout/withdrawal rate of 20%. The intervention duration for all the study participants is 90 days.

Eligibility Criteria

Inclusion

Inclusion criteria:

  • Males aged 45 to 80 years (inclusive of both ages) with a diagnosis of BPHestablished by a surgeon/nephrologist/urologist within the last 3 months and havingany one of the two clinical as well as one of the radio-diagnostic parameters:- a) Clinical parameter: i) History of lower urinary tract symptoms ii) Rectalexamination indicating increased prostate size. b) Radio-diagnostic parameter: i)Uroflowmetry (less than 20 ml/sec maximum flow rate [Qmax]) ii) UltrasoundSonography (USG) - Enlargement of the central gland with a calculated urine volumeexceeding 30 mL and increased post-micturition.

  • Moderate symptoms with an IPSS Score more than or equal to 8-19.

  • No signs of prostate cancer as indicated by 1-3 U/L of Prostatic Acid Phosphatase (PAP) in serum.

  • Fasting blood glucose (FBG) less than 125 mg/dL.

  • Willing to give voluntary written informed consent and adhere to all therequirements of the study.

Note: Only biological males will be included. During screening I, if participants are currently on drug/ supplement for BPH, a washout period of 10±2 days will be provided. After this period, the participant will be rescheduled for screening IA.

Exclusion

Exclusion Criteria:

  • Males with no signs of inflammation as assessed by Erythrocyte Sedimentation Rate (ESR) of more than or equal to 20 mm/hr.

  • Males with more than or equal to 3.5 ng/mL of PSA in serum.

  • Males diagnosed with prostate cancer.

  • Males who have recently started a bladder-training program within the last 30 days.

  • Males who have undergone urogenital surgery.

  • Males who have had a bladder biopsy and/or cystoscopy and biopsy within the last 30days.

  • Males who have had an indwelling catheter or practiced self-catheterization, and/orurethral stricture within the last 30 days.

  • Males diagnosed with obstructive renal/urinary tract calculi.

  • Males who have been medically diagnosed with chronic persistent local pathology (i.e., interstitial cystitis, prostatitis, etc.)

  • Males with chronic inflammatory diseases such as Rheumatoid arthritis (RA),Ulcerative colitis, and Chronic obstructive pulmonary disease (COPD).

  • Males receiving or prescribed anticoagulation therapy.

  • Males who have been diagnosed with severe renal and/or hepatic insufficiency.

  • Males who have been diagnosed with genital anatomical deformities.

  • Males with a history of uncontrolled diabetes mellitus, uncontrolled hypertension (SBP/DBP ≥ 140/90 mmHg1 with or without medication), thyroid disorders, spinal cordinjury, uncontrolled psychiatric disorder, and/or abnormal secondary sexualcharacteristics.

  • Males who have a history of chronic alcohol (defined as consuming more than 5 drinkson any day or more than 15 drinks/week2) and/or illicit drug abuse.

  • Males who have participated in any other clinical study during the last 30 days.

Study Design

Total Participants: 95
Treatment Group(s): 2
Primary Treatment: Placebo
Phase:
Study Start date:
August 05, 2024
Estimated Completion Date:
January 15, 2025

Connect with a study center

  • Parul Sevashram Hospital

    Vadodara, Gujarat 391760
    India

    Site Not Available

  • Sarjanam Hospital

    Vadodara, Gujarat 390012
    India

    Site Not Available

  • NKP Salve Institute of Medical Science and Research Centre and Lata Mangeshkar Hospital

    Nagpur, Maharashtra 440025
    India

    Site Not Available

  • Bhalerao Clinics

    Pune, Maharashtra 411045
    India

    Site Not Available

  • Pawana Hospital

    Pune, Maharashtra 410506
    India

    Site Not Available

  • Rising Medicare Hospital Name of

    Pune, Maharashtra 141014
    India

    Site Not Available

  • Jaipur National University of Medical Science and Research Centre Name of

    Jaipur, Rajasthan 7060924809
    India

    Site Not Available

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