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| ID | Type | Description | Link |
|---|---|---|---|
| 2011-005307-33 | EudraCT Number |
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Inflammation is reported as one of the most recent hypotheses to explain BPH. Recent published works pointed out that urine and serum markers could be used for detection of prostatic inflammation.
The aim of the study is to assess the activity on inflammation biomarkers (serum and urine inflammation markers) of Permixon® 160 mg hard capsule and Tamsulosine Arrow LP in the treatment of urinary symptoms related to BPH.
The potential links between serum and urinary markers of inflammation and BPH clinical symptoms at baseline and on treatment will be explored.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Tested product | Experimental |
| |
| Comparator | Active Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Permixon® 160 mg | Drug | Oral administration - 160 mg twice daily. |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Change from baseline of Inflammation Biomarkers | "Inflammation biomarkers assay in patients suffering from Benign Prostatic Hyperplasia at Day 1, Day 30 and Day 90 :
| Day 1 (baseline), Day 30, Day 90 |
| Measure | Description | Time Frame |
|---|---|---|
| Change from baseline of urinary symptoms | Urinary symptoms assessed by International Prostate Symptom Score (I-PSS) (self-administered questionnaire) | Day 1 (baseline), Day 30, Day 90 |
| Change from baseline of quality of life |
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Inclusion Criteria:
Male patient
Between 45 and 85 years old.
Patient with bothersome lower urinary tract symptoms such as pollakiuria (daytime or night time), urgency, sensation of incomplete voiding, delayed urination or weak stream, existing for over 12 months
I-PSS ≥ 10 at selection visit and ≥ 12 at randomisation visit (visit 2)
Stable patient's disease at randomisation defined as an absolute difference of 2 or less on I-PSS between selection and randomisation visits (visit 1 and visit 2)
I-PSS QoL score ≥ 3 evaluated at selection and randomisation visits,
5 mL/s ≤ maximum urinary flow rate < 15 mL/s for a voided volume ≥ 150 mL and ≤ 500 mL evaluated at randomisation visit (2 measurements if necessary)
Prostatic volume ≥30 cm³ determined by transrectal ultrasound at randomisation visit (visit 2)
Serum total PSA at randomisation visit (visit 2) :
Patient able to understand and sign the informed consent and understand and fill in self-questionnaires
Exclusion Criteria:
Post-void residual urine volume > 200 mL (by suprapubic ultrasound) at randomisation visit (visit 2).
Urological history :
Patient with history of surgery of the prostate, bladder neck or pelvic region
Any local and/or systemic inflammation disorders at selection and randomisation visit
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Angers | France | |||||
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| Tamsulosine Arrow LP |
| Drug |
Oral administration - 0.4 mg daily. |
|
| Placebo matching Permixon® 160 mg | Drug | Oral administration - twice daily. |
|
| Placebo matching Tamsulosine Arrow LP | Drug | Oral administration - daily. |
|
Impact of symptoms on quality of life on the basis of the I-PSS quality of life question scored by the patient
| Day 1 (baseline), Day 30, Day 90 |
| Change from baseline of sexual activity | Sexual activity assessed by the Male Sexual Function questionnaire (MSF-4) (self-administered questionnaire) | Day 1 (baseline), Day 30, Day 90 |
| Change from baseline of maximum urinary flow rate | Uroflowmetry performed using an electronic flow meter. | Day 1 (baseline), Day 30, Day 90 |
| Change from baseline of prostate volume | Prostate volume determined by transrectal ultrasound | Day 1 (baseline), Day 30, Day 90 |
| Change from baseline of post-void residual urine volume (PVR) | Post-void residual urine volume determined by suprapubic ultrasound. | Day 1 (baseline), Day 30, Day 90 |
| Number of adverse events | Number of adverse events | up to 90 days |
| Bordeaux |
| France |
| Cornebarrieu | France |
| Créteil | France |
| La Tronche | France |
| Le Fousseret | France |
| Limoges | France |
| Lyon | France |
| Marseille | France |
| Nice | France |
| Paris | France |
| Saint-Orens-de-Gameville | France |
| Segré | France |
| Seysses | France |
| Tiercé | France |
| Toulouse | France |
| Bari | Italy |
| Catanzaro | Italy |
| Florence | Italy |
| Genova | Italy |
| Milan | Italy |
| Perugia | Italy |
| Pisa | Italy |
| Trieste | Italy |
| Lisbon | Portugal |
| Porto | Portugal |
| A.Coruna | Spain |
| Barcelona | Spain |
| Bilbao | Spain |
| Madrid | Spain |
| Sabadell | Spain |
| Seville | Spain |
| ID | Term |
|---|---|
| D011470 | Prostatic Hyperplasia |
| ID | Term |
|---|---|
| D011469 | Prostatic Diseases |
| D005832 | Genital Diseases, Male |
| D000091662 | Genital Diseases |
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |
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| ID | Term |
|---|---|
| C040972 | saw palmetto extract |
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