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Hyperplasia clinical trials

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NCT ID: NCT01925586 Completed - Clinical trials for Atypical Ductal Hyperplasia (ADH) of the Breast

Atypical Lesions of the Breast: Close Observation Versus Excision (ALCOVE)

ALCOVE
Start date: August 2013
Phase:
Study type: Observational

This study is designed to look at whether it is feasible to observe women with atypical ductal hyperplasia (ADH) of the breast, or whether surgical excision is necessary.

NCT ID: NCT01924988 Completed - Clinical trials for Benign Prostatic Hyperplasia

Prostate Embolization for Benign Prostatic Hyperplasia

Start date: August 2013
Phase: Phase 1/Phase 2
Study type: Interventional

This is a Phase I/II investigator sponsored FDA-approved Investigational Device Exemption protocol, with the primary goal of determining the safety of prostatic artery embolization (PAE) for benign prostatic hyperplasia. Our primary goal is to document the frequency of side effects, particularly bladder and rectal complications, which may occur as a result of this procedure. Secondarily, the study will provide preliminary data to determine its effectiveness in diminishing obstructive symptoms associated with BPH.

NCT ID: NCT01922375 Completed - Clinical trials for Lower Urinary Tract Symptoms Associated With Benign Prostatic Hyperplasia

Clinical Trial to Evaluate the Efficacy and Safety of Naftopidil in Male Patients With Lower Urinary Tract Symptoms Associated With Benign Prostatic Hyperplasia

Start date: December 2011
Phase: Phase 4
Study type: Interventional

This study is designed to evaluate the efficacy and safety of Naftopidil in Korean male patients with with lower urinary tract symptoms associated with benign prostatic hyperplasia. The investigators hypothesized that Naftopidil which came onto marcket in Japan would effect in improvement of voiding and storage difficulty. Design: Placebo-controlled, Randomized, Double-blind, Double-dummy, Parallel group, Fixed dose design

NCT ID: NCT01912339 Completed - Clinical trials for Benign Prostatic Hyperplasia

Safety and Efficacy Study for the Treatment of BPH (Enlarged Prostate)

REZUM
Start date: July 2013
Phase: N/A
Study type: Interventional

To evaluate the safety and efficacy of the Rezūm System and assess its effect on urinary symptoms secondary to benign prostatic hyperplasia (BPH).

NCT ID: NCT01905046 Active, not recruiting - Clinical trials for Ductal Breast Carcinoma in Situ

Metformin Hydrochloride in Preventing Breast Cancer in Patients With Atypical Hyperplasia or In Situ Breast Cancer

Start date: November 23, 2015
Phase: Phase 3
Study type: Interventional

This randomized phase III trial studies metformin hydrochloride to see how well it works compared to placebo in preventing breast cancer in patients with atypical hyperplasia or in situ breast cancer. Chemoprevention is the use of certain drugs to keep cancer from forming. The use of metformin hydrochloride may prevent breast cancer.

NCT ID: NCT01896973 Terminated - Clinical trials for Benign Prostatic Hyperplasia (BPH)

Safety and Initial Efficacy Study of the Vortx Rx for Treatment of Benign Prostatic Hyperplasia (US)

Start date: July 2013
Phase: N/A
Study type: Interventional

The HistoSonics' Histotripsy BPH Device, the Vortx Rx, is a portable ultrasound therapy device. The purpose of this study is to assess and monitor the performance of the Vortx Rx for initial safety and efficacy for the treatment of Benign Prostatic Hyperplasia.

NCT ID: NCT01892332 Completed - Clinical trials for TURP(Transurethral Resection of Prostate)

The Effective Concentration of Lidocaine With Fentanyl in Lumbar Epidural Anesthesia for Transurethral Resection of Prostate(TURP) in Elderly Patients

Start date: June 2013
Phase: N/A
Study type: Interventional

Epidural lidocaine is widely used in anesthesia for urologic or lower abdominal surgery because of its rapid onset. But the epidural anesthesia using high concentration of lidocaine may cause excessive motor block and unwanted side effects such as nausea, vomiting and hypotension. This is a study to determine the effective concentration of lidocaine with fentanyl in lumbar epidural anesthesia for transurethral resection of prostate in elderly patients.

NCT ID: NCT01886547 Completed - Prostate Cancer Clinical Trials

2013 Annual National Digital Rectal Exam (DRE) Day Study

Start date: June 2013
Phase: N/A
Study type: Observational [Patient Registry]

We aim to determine the effectiveness of 2013 "Mag paDRE ka" programme in increasing general public awareness on prostate health and promoting prostate health assessment among Filipino males aged 40 or older.

NCT ID: NCT01876836 Not yet recruiting - Clinical trials for Prostate Hyperplasia

Clasic Laryngeal Mask Airway(C-LMA) and I-gel Releated Regurgitation and Complications

C-LMA
Start date: July 2013
Phase: Phase 4
Study type: Interventional

1. i-gel 2. C-LMA Compare the effect on gastroeosephageal reflux Postoperative complicatios.

NCT ID: NCT01876706 Completed - Clinical trials for Benign Prostatic Hyperplasia

UroLift System TOlerability and ReCovery When Administering Local Anesthesia

LOCAL
Start date: April 2013
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate procedure tolerability and surgical recovery following the UroLift® system procedure when conducted with local anesthesia in subjects with symptomatic benign hyperplasia (BPH). Primary effectiveness will be achieved by looking at the Quality of Recovery Visual Analog Scale (QoR VAS) by the one month follow-up visit.