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Hyperplasia clinical trials

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NCT ID: NCT03246880 Completed - Clinical trials for Benign Prostatic Hyperplasia

Clinical Trial To Evaluate the Efficacy and Safety of CKD-397 in Benign Prostatic Hyperplasia Patients

Start date: September 2015
Phase: Phase 3
Study type: Interventional

A Multicenter, Randomized, Double-blind, Active-controlled, Parallel group, Phase III Clinical Trial To Evaluate the Efficacy and Safety of CKD-397 in Benign Prostatic Hyperplasia Patients.

NCT ID: NCT03243565 Not yet recruiting - Clinical trials for Respiratory Tract Infections

Effect of OM-85 on Respiratory Tract Infections and Adenoid Tissue in Children With Adenoid Hypertrophy

Start date: November 1, 2017
Phase: Phase 4
Study type: Interventional

Clinical research question: Can OM-85 reduce the recurrence of respiratory tract infections (RTIs) in children with AH by stimulating the immunological response of the host and therefore, as a consequence reduce the size of adenoid tissue in children with adenoid hypertrophy? Can this prevent further complications such as surgery need? Half of participants will receive OM-85, while other half will receive a placebo.

NCT ID: NCT03241888 Completed - Clinical trials for Atypical Endometrial Hyperplasia

Megestrol Acetate Plus LNG-IUS in Young Women With Endometrial Atypical Hyperplasia

Start date: July 4, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

To see if megestrol acetate plus Levonorgestrel-releasing intrauterine system (LNG-IUS) will not be inferior to returning the endometrial tissue to a normal state than megestrol acetate or LNG-IUS alone in patients with endometrial atypical hyperplasia.

NCT ID: NCT03240939 Completed - Clinical trials for Benign Prostatic Hyperplasia

Pharmacokinetics and Safety/Tolerability of YY-201 in Comparison to Dutasteride and Tadalafil

Start date: March 27, 2017
Phase: Phase 1
Study type: Interventional

A randomized, open label, single dose, two-way crossover clinical trial to investigate the pharmacokinetics and safety/tolerability of YY-201 in comparison to Dutasteride and Tadalafil administered in healthy male volunteers

NCT ID: NCT03239652 Recruiting - Clinical trials for Benign Prostatic Hyperplasia (BPH)

Taiwan ACE Beads for Embolization Therapy in Symptomatic Benign Prostatic Hyperplasia

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

In this proposal, the investigators plan to conduct a clinical trial to validate the efficacy and safety of microspheres (T-ACE Beads).

NCT ID: NCT03231644 Recruiting - Fibrous Dysplasia Clinical Trials

Fibrous Dysplasia, McCune-Albright Syndrome Patient Registry

Start date: October 31, 2016
Phase:
Study type: Observational [Patient Registry]

The FD/MAS Patient Registry is an IRB-approved research study that that invites the patients and families to help answer some of the biggest questions about FD/MAS by completing questionnaires about their lives with FD or MAS. Have you enrolled in the FD/MAS Patient Registry yet? Are you up-to-date on your surveys? Take a trip to www.fdmasregistry.org today to learn more about the project, enroll, complete your surveys, or make sure you aren't due to provide more info! The FD/MAS Patient Registry: Your story powers research.

NCT ID: NCT03230721 Completed - Clinical trials for Lower Urinary Tract Symptoms

ThuLEP vs. HoLEP vs. Monopolar Enucleation in Management of BPH

Start date: January 15, 2015
Phase: N/A
Study type: Interventional

Today, endoscopic enucleation of the prostate (EEP) has been recognized a method of choice for treatment of benign prostatic hyperplasia (BPH) of any size, including large-sized glands (>80 cc). The goal of our study was to compare perioperative efficacy, functional outcomes and safety of different techniques of endoscopic enucleation of the prostate (monopolar enucleation, holmium laser enucleation, thulium laser enucleation) in a single center.

NCT ID: NCT03229967 Completed - Clinical trials for Bronchopulmonary Dysplasia

Gastrointestinal Microbiome Influence on the Development of Bronchopulmonary Dysplasia

MiBPD
Start date: July 5, 2017
Phase:
Study type: Observational

The purpose of this study is to advance our knowledge of the factors that contribute to the development of bronchopulmonary dysplasia (BPD), a chronic lung affecting premature infants. Specifically, the investigators will determine the complexity of the gut microbiota, the genera of the bacteria that naturally live in the gut, and determine if the relative diversity of the gut bacteria is a prognostic indicator of BPD. To accomplish this, the investigators propose to characterize the microbiota of human premature newborns with BPD, then validate this potential mechanism in mice. The investigators will enroll very low birthweight premature infants admitted to the neonatal intensive care units (NICU) at Le Bonheur Children's Hospital and Regional One Health that are at high risk to develop BPD. A cohort of well full term newborns will also be enrolled. Non-invasive stool samples will be obtained weekly over the first month of life. Infants that eventually develop BPD will be paired with infants that did not develop BPD. Stool samples from these infants will be sent for analysis. The investigators expect that reduced complexity of the gut microbiome is associated with BPD. The investigators will model the contribution of reduced microbiome complexity to the risk to develop BPD or death, as well as the association with disease severity. The project investigates important factors leading to the development of BPD, and has the potential to directly translate to therapy for the most significant pulmonary complication of prematurity.

NCT ID: NCT03228485 Active, not recruiting - Clinical trials for Lower Urinary Tract Symptoms

Benign Prostatic Hyperplasia (BPH) Mobile Application Pilot Study

Start date: April 4, 2019
Phase:
Study type: Observational

This study assesses the feasibility, and acceptability of a (mobile) application for men presenting at their physician's office with LUTS/BPH; starting with medical therapy and naïve for treatment. Patients will be enrolled in the study by their physician (GP or urologist). The patients will receive a daily medication reminder including frequent feedback on medication adherence. Furthermore, standard questionnaires will be filled out via the application. The hypothesis of this pilot study is that application is feasible and accepted in this group of patients.

NCT ID: NCT03209843 Completed - Clinical trials for Ischemic Cardiomyopathy

Post-stenting Assessment of Reendothelialization With OFDI After CTO Procedure (PERFECTO)

PERFECTO
Start date: March 7, 2018
Phase: N/A
Study type: Interventional

The objective of PERFECTO is to assess the reendothelialization at 3 months after successfully CTO percutaneous intervention (PCI) with new generation drug eluting stent (DES) by OFDI analysis. Designed as a multicentric, observational and prospective study which will be conducted at University Hospital of Poitiers (France), a systematic OFDI analysis will be realized immediately after CTO-PCI and at 3 months. Known as major predictive factors of stent thrombosis, percentages of malapposition, uncovered struts and neointimal hyperplasia proliferation will be measured over the entire length of each stent implanted combining in a composite primary endpoint.