Observational Study in Patients Suffering From Benign Prostatic

Clinical Trial Summary

The primary objective of this observational study was the assessment of prognosis factors for having recourse to prostatic surgery in patients with BPH who were administered class-1 alpha blockers. The secondary objectives were the assessment of the time from alpha-adrenergic blockade treatment initiation to surgery and the evolution of patients during the study.

See also
Status	Clinical Trial	Phase
Completed	`NCT02578953` - Bioequivalence Study of Dutasteride Capsules in Healthy Japanese Male Subjects	Phase 1
Terminated	`NCT02396420` - Prostate Artery Embolization as a Treatment for Benign Prostatic Hyperplasia in Men With Prostates Larger Than 90 Grams	Phase 2
Terminated	`NCT04398966` - Prostatic Artery Embolization vs Medication for Benign Prostatic Hyperplasia	N/A
Not yet recruiting	`NCT06452927` - EEP in Patients With Urodynamically Proven DU/DA	N/A
Completed	`NCT02947958` - Teleconsultation in Counter-reference Between Tertiary and Primary Care for Patients With Benign Prostatic Hyperplasia	N/A
Completed	`NCT01937871` - A Study of Tadalafil in Men With Benign Prostatic Hyperplasia (BPH) and Erectile Dysfunction (ED)	Phase 3
Completed	`NCT00427882` - Male Sexual Health Questionnaire (MSHQ) - Sexual Function Study	Phase 4
Completed	`NCT02244320` - Observational Study in Patients With Functional Benign Prostatic Hyperplasia Symptoms Who Switched From Phytotherapy to ALNA® (Tamsulosin)	N/A
Completed	`NCT01254071` - A Study to Determine the Bioavailability of a Fixed Dose Combination Product of Dutasteride (0.5mg) and Tamsulosin Hydrochloride (0.2mg) Relative to Co-administration of the Individual Components in Healthy Male Subjects of North East Asian and Non-Asian Ancestry.	Phase 1
Recruiting	`NCT04108871` - Whether Transperineal Prostate Biopsy Under Local-anaesthesia Using a Transperineal-access System is Non-inferior to Standard Transrectal Biopsy to Detect Prostate Cancer in Biopsy-naïve Men	N/A
Recruiting	`NCT05686525` - Clinical Trial on the Effectiveness of TUMT Compared to PAE in Reducing Severe LUTS in Men With BPH	N/A
Completed	`NCT01957189` - This Will be an Open-label, Three-period, Fixed-sequence Study to Evaluate the Drug-drug Interaction, Pharmacokinetics and Safety of Dutasteride and Tamsulosin When Administered Alone and In-combination in Chinese Healthy Male Volunteers. The Study Will Last Approximately Eleven Weeks. Blood Samples	Phase 1
Completed	`NCT00316732` - Observational AVODART (Dutasteride) Study In Benign Prostatic Hyperplasia Subjects - OASIS	N/A
Completed	`NCT02715401` - PK and Safety of HCP1303 and Co-administration of HGP1201, HIP1402 Under Fed Condition in Healthy Male Volunteers	Phase 1
Recruiting	`NCT02278679` - Digital Rectal Exam Proficiency Tool	N/A
Completed	`NCT01376258` - Benefits of Adherence to 5-alpha Reductase Inhibitor Treatment in Men With Enlarged Prostate: An Assessment of Medicare and Medicaid Patients Using the MarketScan Database	N/A
Completed	`NCT01482676` - The Role of microRNAs in Organ Remodeling in Lower Urinary Tract Dysfunction	N/A
Completed	`NCT00822952` - Prostate Mechanical Imager (PMI) Clinical Bridging Study	N/A
Completed	`NCT00527605` - Dutasteride 0.5mg For The Treatment Of Chinese Patients With Benign Prostatic Hyperplasia (BPH)	Phase 3
Terminated	`NCT00563485` - Randomized Trial Comparing Terazosin 5 mg Daily and Doxazosin GITS 4 mg Daily for Trial Without Catheter in Acute Urinary Retention With Long Term Follow up	N/A

NCT number	NCT02244307
Study type	Observational
Source	Boehringer Ingelheim
Contact
Status	Completed
Phase	N/A
Start date	January 2000

Observational Study in Patients Suffering From Benign Prostatic Hyperplasia Treated With Alpha-adrenergic Blockade

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms