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Evaluation of the Effectiveness of Terazosin in Patients with Nocturia due to Prostate Hyperplasia

Evaluation of the Effectiveness of Terazosin in Patients with Nocturia due to Prostate Hyperplasia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CRIS
Registry ID
KCT0004837
Enrollment
82
Registered
2020-03-17
Start date
2020-03-09
Completion date
Unknown
Last updated
2020-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Drug : Patients participating in this clinical study are required to take 2 mg or 5 mg of terrazocin once a day for the next 8 weeks, depending on the significance of the injection.

Sponsors

Hanyang University Guri Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. An adult male over 19 years of age 2. Persons with an IPSS total score of 8 or higher 3. Persons with a maximum urinary speed (Qmax) of less than 15mL/s 4. Persons with a single urinary volume of 150 mL or higher 5. Persons with more than one night urination 6. Those who have agreed to participate in this research under the signature of their own handwriting

Exclusion criteria

Exclusion criteria: 1. Those who are overreacting to Alpha-Blocker drugs 2. Person with bladder neck stenosis and urinary tract stenosis 3. Persons with renal dysfunction (Creatine concentration in the serum >2.0 mg/dL) 4. A person with severe liver failure or with a history of illness. 5. Those with severe cardiovascular disease 6. A person with severe low blood pressure 7. Other persons who are not qualified to participate in this study as the Director of Research judges

Design outcomes

Primary

MeasureTime frame
Evaluate improvement of IPSS total score

Secondary

MeasureTime frame
change in the number of nocturia;LSEQ scores;Quality of life improvement

Countries

Korea, Republic of

Contacts

Public ContactHyeonkyung Kim

Hanyang University Guri Hospital

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026