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Hyperplasia clinical trials

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NCT ID: NCT00648323 Completed - Prostate Clinical Trials

Evaluation Of The Efficacy And Safety Of The Doxasozin Gastrointestinal Therapeutic System (GITS) In Patients With Prostate Enlargement

Start date: November 2003
Phase: Phase 4
Study type: Interventional

The primary objectives were to determine the efficacy and safety of the GITS formulation of Doxazosin in Taiwanese patients with prostate enlargement.

NCT ID: NCT00645034 Completed - Clinical trials for Benign Prostatic Hyperplasia

A Study to Investigate the Effects on Blood Pressure and Pulse Rate of a Single 100mg Dose of Sildenafil in Patients With Benign Prostatic Hyperplasia Who Are Being Treated With Doxazosin

Start date: November 2002
Phase: Phase 2
Study type: Interventional

To investigate the effects of a single dose of sildenafil (100 mg) or placebo on blood pressure and pulse rate in subjects taking doxazosin for benign prostatic hyperplasia (BPH). To investigate the pharmacokinetics of doxazosin when co-administered with sildenafil 100 mg, and to investigate the safety and toleration of sildenafil 100 mg when co-administered with doxazosin.

NCT ID: NCT00637715 Completed - Clinical trials for Benign Prostatic Hyperplasia

Once Daily Given Alfuzosin in the Treatment of BPH

Start date: October 2003
Phase: Phase 4
Study type: Interventional

Collection of the data on the safety and efficacy of the once daily administration of the alfuzosin preparation /Alfetim Uno® l0 mg/ at patients with lower urinary tract symptoms/complaints rendering possible the presence of benign prostatic hyperplasia, in the course of everyday practice

NCT ID: NCT00637481 Completed - Breast Cancer Clinical Trials

A Phase I Prevention Study of Atorvastatin in Women at Increased Risk for Breast Cancer

Start date: March 2008
Phase: Phase 1
Study type: Interventional

Chemoprevention is the use of certain drugs to keep cancer from forming. The use of atorvastatin (Lipitor) may prevent breast cancer. This randomized phase I trial is studying the best dose of atorvastatin in preventing breast cancer in women at increased risk for breast cancer.

NCT ID: NCT00627276 Completed - Breast Cancer Clinical Trials

Omega-3 Fatty Acids in Treating Women With Newly Diagnosed Ductal Carcinoma In Situ and/or Atypical Ductal Hyperplasia

Start date: December 2007
Phase: N/A
Study type: Interventional

RATIONALE: Polyunsaturated fatty acids are important for normal growth and development. One type, called omega-3 fatty acids (found in fish, fish oil, and some other foods), may affect the growth of abnormal breast cells. PURPOSE: This randomized pilot trial is studying how well omega-3 fatty acids work in treating women with newly diagnosed ductal carcinoma in situ and/or atypical ductal hyperplasia.

NCT ID: NCT00623740 Completed - Clinical trials for Bronchopulmonary Dysplasia

PREMILOC Trial to Prevent Bronchopulmonary Dysplasia in Very Preterm Neonates

PREMILOC
Start date: April 2008
Phase: Phase 3
Study type: Interventional

There is increasing evidence linking a fetal and early neonatal systemic inflammatory response syndrome to the subsequent development of bronchopulmonary dysplasia (BPD) and white matter injury (WMI) in very preterm infants. Babies with evidence of adrenal insufficiency early in life may not be able to control the inflammatory response and are thereby more likely to develop BPD than babies who do not show such evidence of inflammation. We designed a randomized controlled trial to test the hypothesis whether very preterm babies at high-risk of BPD, treated with low doses of HC during the first 10 days of life, are more likely to survive without BPD at 36 weeks of post-menstrual age (PMA), compared to babies treated with placebo.

NCT ID: NCT00621985 Completed - Clinical trials for Adrenal Hyperplasia, Congenital

Dexamethasone Treatment of Congenital Adrenal Hyperplasia

Start date: April 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if dexamethasone given at night is a more effective treatment for congenital adrenal hyperplasia in young children than standard three times per day hydrocortisone. Our hypothesis is that nocturnal dexamethasone will lead to more efficient suppression of the hypothalamic-pituitary-adrenal axis. We performed a cross-over trial comparing hormonal control during two 24-hour hospitalizations, one on hydrocortisone and one on nocturnal dexamethasone.

NCT ID: NCT00620087 Completed - Clinical trials for Atypical Ductal Hyperplasia

Molecular Breast Imaging in Women With Atypia and LCIS

Start date: August 2003
Phase: N/A
Study type: Interventional

We aim to determine if Molecular Breast Imaging (a new nuclear medicine technique developed at Mayo) can identify malignant breast lesions in women who have atypical ductal hyperplasia, atypical lobular hyperplasia, or lobular carcinoma in situ.

NCT ID: NCT00609596 Completed - Clinical trials for Prostatic Hyperplasia

A Study To Compare 3 Different Formulations Of Tamsulosin At Steady State.

Start date: February 26, 2008
Phase: Phase 1
Study type: Interventional

Dutasteride and tamsulosin are to treat benign prostatic hyperplasia. Studies show that when given together, there is more improvement in symptoms than either drug alone. In this study, we are looking to see if 2 different formulations of tamsulosin in our combination capsules are the same after 7 days of dosing as the US commercial tamsulosin and dutasteride.

NCT ID: NCT00596011 Completed - Clinical trials for Prostatic Hyperplasia

Study of Polyphenon E in Men With High-grade Prostatic Intraepithelial Neoplasia

Start date: November 14, 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study was to determine whether the daily consumption of decaffeinated green tea catechins (Polyphenon E®) for 1 year reduces the rate of progression to prostate cancer (PCa) in men diagnosed with HGPIN or ASAP. The aim was to recruit and treat 240 (120 men/arm) men diagnosed with the prostate condition HGPIN or ASAP with a capsule form of standardized green tea extract called Polyphenon E or placebo for a 12-month period and see if it can prevent progression of the prostate condition to prostate cancer. Investigators wanted to see if Polyphenon E reduces lower urinary tract symptoms and if this can be taken safely over one year. Investigators wanted to study how Polyphenon E is able to slow the progression to prostate cancer, or the mechanism of action of Polyphenon E. If the safety and the effects of Polyphenon E on slowing down the progression of prostate cancer is shown in our study, this will be a safe way of treating men who are at high risk or men like you who have a prostate condition that increases your chances of getting prostate cancer, so that we can prevent prostate cancer in the future.