Phase
Condition
Prostate Disorders
Bladder Disorders
Treatment
Placebo
Fucoidan extracted from Undaria pinnatifida (UPF)
Clinical Study ID
Ages 45-80 Male
Study Summary
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
Connect with a study center
Parul Sevashram Hospital
Vadodara, Gujarat 391760
IndiaSite Not Available
Sarjanam Hospital
Vadodara, Gujarat 390012
IndiaSite Not Available
NKP Salve Institute of Medical Science and Research Centre and Lata Mangeshkar Hospital
Nagpur, Maharashtra 440025
IndiaSite Not Available
Bhalerao Clinics
Pune, Maharashtra 411045
IndiaSite Not Available
Pawana Hospital
Pune, Maharashtra 410506
IndiaSite Not Available
Rising Medicare Hospital Name of
Pune, Maharashtra 141014
IndiaSite Not Available
Jaipur National University of Medical Science and Research Centre Name of
Jaipur, Rajasthan 7060924809
IndiaSite Not Available

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