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Hyperplasia clinical trials

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NCT ID: NCT00169585 Completed - Clinical trials for Prostatic Hyperplasia

Levofloxacin For The Management Of Patients With Abnormal Prostate Specific Antigen (PSA)

Start date: March 2005
Phase: Phase 3
Study type: Interventional

Multicentric, national, prospective, parallel group, controlled. The Subjects in every center will be randomized and assigned to the pharmacologic arm or the one with the biochemical monitoring

NCT ID: NCT00159406 Active, not recruiting - Clinical trials for Benign Prostatic Hyperplasia

Laser Prostatectomy Database and Registry

Start date: October 2003
Phase:
Study type: Observational

STATEMENT OF PURPOSE: Transurethral resection of the prostate (TURP) is the standard surgical intervention for obstructive benign prostatic hyperplasia (BPH) in all but the largest of glands, which are typically treated with open simple prostatectomy. Recently, new generation lasers (holmium and potassium titanyl phosphate [KTP]) have been utilized for BPH treatment. Long-term follow-up of laser prostatectomy outcomes must be documented to fully characterize the degree of voiding improvement achievable by these new techniques, the durability of these outcomes, and the safety profiles of these procedures.

NCT ID: NCT00151710 Completed - Clinical trials for Congenital Adrenal Hyperplasia

Effects of Pioglitazone in Congenital Adrenal Hyperplasia

Start date: n/a
Phase: N/A
Study type: Interventional

Congenital adrenal hyperplasia, an autosomal recessive condition, is mainly caused by mutations in the gene 21-hydroxylase and is treated with glucocorticoids in a slightly supraphysiological dose. Adult patients seem to be characterized by insulin resistance, which may be caused by the glucocorticoids and/or the accompanying obesity. The hypothesis of this study is that pioglitazone can improve insulin sensitivity and correlated cardiovascular risk factors in this specific group of patients. This will be tested in a randomized, placebo-controlled, cross-over trial; insulin sensitivity will be quantified by euglycemic hyperinsulinemic clamp studies.

NCT ID: NCT00143221 Completed - Impotence Clinical Trials

Effectiveness and Safety of Viagra in Men With ED and LUTS Due to Benign Prostatic Hyperplasia (BPH)

Start date: March 2004
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether Viagra is effective in treating erectile dysfunction and lower urinary tract symptoms in men affected by both conditions.

NCT ID: NCT00130767 Active, not recruiting - Clinical trials for Benign Prostatic Hyperplasia

Kinetics of the Finasteride Prostate Induced Apoptosis

Start date: December 2004
Phase: Phase 4
Study type: Interventional

The aim of this study is to evaluate the mechanisms involved in the apoptosis induced by a treatment of finasteride on benign prostate hyperplasia (BPH). Five sets of patients who need a surgical procedure because of low tract urinary symptoms are randomly attributed to one of five sets of treatment: 0, 7, 14, 21 or 28 days of finasteride treatment before the day of the procedure. Prostate histological fragments are conditioned for molecular and histologic studies.

NCT ID: NCT00127569 Terminated - HIV Infections Clinical Trials

Rituximab in the Treatment of HIV Associated Multicentric Castleman Disease Dependent on Chemotherapy

Start date: May 2003
Phase: Phase 2
Study type: Interventional

This trial is aimed to study the efficacy of 4 weekly cycles of rituximab in HIV-infected patients with multicentric Castleman disease (giant lymph node hyperplasia) dependent on chemotherapy. Efficacy is assessed by the complete response rate at day 60. The patients are followed until day 365.

NCT ID: NCT00127179 Completed - Clinical trials for Benign Prostatic Hyperplasia

A Study of an Investigational Study Drug for Benign Prostatic Hyperplasia (0906-140)

Start date: January 1, 2004
Phase: Phase 3
Study type: Interventional

The purpose of this trial is to determine the efficacy and safety of an investigational drug in patients with benign prostatic hyperplasia.

NCT ID: NCT00123188 Terminated - Clinical trials for Endometrial Hyperplasia

Ultrasound and Endometrial Hyperplasia

Start date: April 2005
Phase: N/A
Study type: Interventional

The investigators hypothesize that endometrial thickness will be a significant predictor of endometrial hyperplasia in a postmenopausal female population with metabolic syndrome: diabetes and/or insulin resistance, hypertension, and obesity.

NCT ID: NCT00123175 Withdrawn - Clinical trials for Endometrial Hyperplasia

Treatment of Endometrial Hyperplasia With an Intrauterine Device (IUD)

Start date: September 2009
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this research is to determine the effectiveness of the intrauterine device (IUD) called Mirena when compared to the Provera tablets used in treating this condition.

NCT ID: NCT00116571 Terminated - Clinical trials for Prostatic Hyperplasia

Photodynamic Therapy (PDT) for Lower Urinary Tract Symptoms (PLUS)

Start date: May 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if transurethral photodynamic therapy with lemuteporfin has a therapeutic effect on lower urinary tract symptoms due to an enlarged prostate. Photodynamic therapy (known as "PDT") is a treatment that uses light to make a drug work. This means the drug is "light-activated". Light-activated drugs do not work until a certain color of light shines on the drug. When the drug and the light combine, they react together to destroy tissue. This study is investigating PDT with lemuteporfin as a possible treatment for an enlarged prostate. PDT with lemuteporfin may destroy overgrown prostate tissue and help urinary symptoms go back to normal.