One-Year Prospective Observational Study of BMI Change Effect of 5-Alpha Reductase Inhibitor in Korean BPH Patients - Full Text View

Sponsors and Collaborators:	Seoul National University Hospital GlaxoSmithKline Seoul National University Bundang Hospital
Information provided by:	Seoul National University Hospital
ClinicalTrials.gov Identifier:	NCT00472251

Purpose

It is widely-accepted that serum testosterone level and BMI (body mass index) representative of the degree of obesity has negative correlation. Considering the fact that obesity is being mentioned as a risk factor for development of prostate cancer as well as other various life-threatening diseases (example: cardiovascular problems), the effect of BPH treatment agents on BMI is a subject that should certainly be elucidated. Meanwhile, to our knowledge, no prospective study has so far been performed on such issue in Asian population. Prior to generating hypothesis of the effect of 5 alpha reductase inhibitor on BMI, the real effect of 5 alpha reductase inhibitor on BMI change in Korean BPH patients has to be observed in real clinical practice. This study will test the effects of one-year medication of 5 alpha reductase inhibitor on BMI among Korean men with BPH.

Condition
Benign Prostatic Hyperplasia

Drug Information available for: Testosterone Methyltestosterone Oxymesterone Testosterone enanthate Testosterone Propionate Testosterone undecanoate Dutasteride

U.S. FDA Resources

Study Type:	Observational
Study Design:	Natural History, Longitudinal, Random Sample, Prospective Study
Official Title:	One-Year Prospective Observational Study of BMI Change Effect of 5-Alpha Reductase Inhibitor in Korean BPH Patients

Further study details as provided by Seoul National University Hospital:

Estimated Enrollment:	100
Study Start Date:	May 2007
Estimated Study Completion Date:	November 2008

Detailed Description:

This study is a prospective, 1-year follow-up, observational study. We are planning to enroll 100 Korean patients with BPH. At each visit, patients’ height, weight, abdominal circumference will be checked. Laboratory parameters including fasting glucose, HbA1c, serum testosterone, free testosterone, sex hormone-binding globulin, estradiol, maximum flow rate (measured by flowmetry) will be tested. Blood test will be performed twice (at baseline and at the end of study). 5mL of blood will be needed at each time from one subject. And total IPSS score will be evaluated after 1 year of treatment of 5 ARI. At every visit, use of above prohibited medicines and other medications will be investigated. In addition, any surgical procedures undertaken during study period will be asked and recorded.

Subjects of study will be allocated into 3 separate groups. Group 1 will be those taking 5 alpha reductase inhibitor (dutasteride) only for 1 year. Group2 will be those who switch from alpha blocker to dutasteride and take dutasteride for 1 year. Group 3 will be composed of those taking both alpha blocker and dutasteride for 1 year.

composed of

Eligibility

Genders Eligible for Study:	Male
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

Male patients with symptomatic BPH
Prostate volume of 30 cm3 or greater measured by transrectal ultrasound
International Prostatic Symptom Score(IPSS) of 9 or greater
Maximum urinary flow rate (Qmax) of 15ml/s or less
No definite evidence of prostate cancer (on transrectal ultrasound, DRE, or etc.)
Given Informed consent

Exclusion Criteria:

Post-void residual more than 250 mL
History of cancer (including prostate cancer) or previous prostatic surgery
Acute urinary retention within 3 months of enrollment
Chronic alcohol abuser and heavy smoker (> 10 cigarettes/day)
History of/current drug abuse including laxatives
Any previous 5 ARI administration
Type 1 DM or Type 2 DM regardless of treatment
Clinically significant endocrine diseases at investigator’s discretion including thyroid diseases.
History of /current bulimia or anorexia nervosa
Regular use of following prohibited medicines within 3 months prior to screening; A. Medicines which can affect salt/water retention such as diuretics, calcium channel blockers, gabapentin, pregabalin, etc B. Medicines which can affect body weight such as sibutramine, orlistat, phentermine, amphetamine, etc.

C. Anti-thyroid medication, thyroxine, cyproheptadine, tranquilizers, systemic corticosteroids, testosterone supplement, or other medications that are known to affect body weight or BMI

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00472251

Contacts

Contact: Sung Kyu Hong, MD, PhD

+82-31-787-7343

hsk823@chol.com

Locations

Korea, Republic of, Kyunggi-do
Seoul National University Bundang Hospital	Recruiting
Seongnam-si, Kyunggi-do, Korea, Republic of, 463-707
Contact: Sung Kyu Hong, MD, PhD +82-31-787-7343 hsk823@chol.com

Sponsors and Collaborators

Seoul National University Hospital

GlaxoSmithKline

Seoul National University Bundang Hospital

Investigators

Principal Investigator:

Sang Eun Lee, MD, PhD

Seoul National University Bundang Hospital

More Information

Publications:

Roehrborn CG, Lee M, Meehan A, Waldstreicher J; PLESS Study Group. Effects of finasteride on serum testosterone and body mass index in men with benign prostatic hyperplasia. Urology. 2003 Nov;62(5):894-9.

Study ID Numbers:	CRT110446
Study First Received:	May 10, 2007
Last Updated:	May 10, 2007
ClinicalTrials.gov Identifier:	NCT00472251
Health Authority:	Korea: Food and Drug Administration

Keywords provided by Seoul National University Hospital:

dutasteride
body mass index
testosterone

Study placed in the following topic categories:

Dutasteride
Testosterone
Hyperplasia
Prostatic Diseases

Prostatic Hyperplasia
Methyltestosterone
Genital Diseases, Male
Testosterone 17 beta-cypionate

Additional relevant MeSH terms:

Pathologic Processes

ClinicalTrials.gov processed this record on January 14, 2009