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RECRUITING
NCT05401032
PHASE2

Proof-of-concept Study to Evaluate the Safety and Efficacy of Tryptophan in Patients with BPH.

Sponsor: Clinical Academic Center (2CA-Braga)

View on ClinicalTrials.gov

Summary

Benign prostatic hyperplasia (BPH) is one of the most prevalent human diseases and a major cause of lower urinary tract symptoms (LUTS). Some men respond to current medical treatment (mainly α-1 adrenoreceptor antagonists and 5 α-reductase inhibitors), but a large proportion of patients continues to need a surgical procedure to treat resistant LUTS or even more serious complications of BPH, creating the emerging necessity for novel pharmacological therapies. Oxitriptan may have a possible positive effect on BPH associated symptoms with probably no impact in sexual function (which is a common side effect of the current drugs for BPH associated symptoms). Also, improvement in symptoms could be higher than that of current drugs used for this condition. This is a single-center parallel group, randomized clinical trial. The study will take place in Hospital de Braga (Urology department). Eligible patients will be randomized to receive tamsulosin 0.4mg (once a day, q.d.) or 5-HTP (5-hidroxitriptophan) 100mg (three times a day, t.i.d.), for 6 months.

Official title: TryptoBPH - Proof-of-concept Study to Evaluate the Safety and Efficacy of Tryptophan in Patients with BPH

Key Details

Gender

MALE

Age Range

50 Years - 74 Years

Study Type

INTERVENTIONAL

Enrollment

70

Start Date

2024-12-20

Completion Date

2026-12-31

Last Updated

2025-01-06

Healthy Volunteers

No

Interventions

DRUG

Tamsulosin

Oral medication, once a day for 6 months.

DRUG

5-hidroxitriptophan

Oral medication, 3 times a day for 6 months.

Locations (1)

Clinical Academic Center - Braga, Association (2CA-Braga)

Braga, Portugal