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Hyperplasia clinical trials

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NCT ID: NCT03558334 Recruiting - Clinical trials for Bronchopulmonary Dysplasia

Human Mesenchymal Stem Cells For Bronchopulmonary Dysplasia

Start date: June 28, 2018
Phase: Phase 1
Study type: Interventional

This study is an open-label, single-center, dose escalation study to evaluate of safety and efficacy of human umbilical cord -derived mesenchymal stem cells (hUC-MSCs) in premature infants for moderate and severe Bronchopulmonary Dysplasia(BPD).

NCT ID: NCT03538977 Recruiting - Clinical trials for Bronchopulmonary Dysplasia

Hydrotherapy in Premature Infants With Bronchopulmonary Dysplasia

Start date: October 11, 2018
Phase: N/A
Study type: Interventional

Premature newborns (PTNB) often develop bronchopulmonary dysplasia (BPD) which can be related to an inability to maintain differences in tonus patterns (extensor and flexor) between the cervical muscles, upper and lower limbs. Babies who develop BPD remain in the neonatal intensive care unit (NICU) for a prolonged period of time, undergoing a large number of painful procedures. Exposure to pain in premature newborns (PTNB) is one of the most damaging factors in the extrauterine environment, also causing stress, which can also interfere with tonus pattern. Therefore, the aim of this study is to evaluate the effects of hydrotherapy on muscular activity, pain, sleep and wakefulness, stress, physiological conditions and the need for oxygen in PTNB with BPD during hospitalization in the neonatal unit. EXPECTED RESULTS: Hydrotherapy is expected to relieve pain, improve sleep quality and reduce oxygen therapy and ventilatory support in hospitalized PTNB babies with BPD.

NCT ID: NCT03521648 Recruiting - Clinical trials for Benign Prostatic Hyperplasia

Database for the Assessment of Efficacy and Safety of BPH Treatment

KSSG-BPH-REG
Start date: July 7, 2017
Phase:
Study type: Observational [Patient Registry]

This registry study aims to collect data on efficacy and safety of different treatments of benign prostatic enlargement (BPE) and lower urinary tract symptoms associated with benign prostatic hyperplasia (BPH-LUTS).

NCT ID: NCT03521063 Recruiting - Clinical trials for Bronchopulmonary Dysplasia

Efficacy of Adding Budesonide to Poractant Alfa to Prevent Bronchopulmonary Dysplasia.

Start date: January 1, 2018
Phase: Phase 4
Study type: Interventional

This study evaluates the addition of budesonide to poractant alfa to prevent bronchopulmonary dysplasia in preterm infants with respiratory distress syndrome. Half of the participants will receive budesonide and poractant alfa in combination, and the other half will receive poractant alfa with saline.

NCT ID: NCT03503721 Recruiting - Clinical trials for Benign Prostatic Hyperplasia

Bipolar Transurethral Enucleation (BipolEP) vs Bipolar Transurethral Resection of the Prostate

Start date: January 18, 2018
Phase: N/A
Study type: Interventional

The aim of this study is to compare two different surgical methods for treating benign prostatic obstruction (BPO). The investigators are going to compare the risks and benefits of bipolar transurethral resection of the prostate (TURP) and bipolar transurethral enucleation of the prostate (BipolEP). Furthermore, the investigators are going to compare the amount of tissue resected per minute, in order to assess the efficiency of each surgical method. It is a prospective, interventional, multi-centre (2 centres total), randomized trial. Approximately 84 patients will be included

NCT ID: NCT03479359 Recruiting - Prostatic Neoplasms Clinical Trials

Learning Curve of Digital Rectal Examination for Prostate Cancer Among Internship

Start date: February 26, 2018
Phase:
Study type: Observational

The investigators conduct this prospective study to investigate the learning curve of digital rectal examination (DRE) for prostate cancer among internship. The investigators want to know how many DRE are usually needed for internship to be performed in urological practice to obtain a stable DRE accuracy.

NCT ID: NCT03463252 Recruiting - Endometrial Cancer Clinical Trials

Value of LNG-IUS as Fertility-preserving Treatment of EAH and EC

Start date: April 1, 2018
Phase: Phase 2/Phase 3
Study type: Interventional

Primary end points: This clinical trial is aimed to analyze the effectiveness of Levonorgestrel-Releasing Intrauterine System (LNG-IUS, Mirena®) in the fertility-sparing treatment of atypical endometrial hyperplasia and early endometrial carcinoma, including pathology response and pregnancy outcome. Second end points: To analyze the appearances of side-effects.

NCT ID: NCT03382158 Recruiting - Neuroblastoma Clinical Trials

International PPB/DICER1 Registry

Start date: December 6, 2016
Phase:
Study type: Observational

Pleuropulmonary blastoma (PPB) is a rare malignant neoplasm of the lung presenting in early childhood. Type I PPB is a purely cystic lesion, Type II is a partially cystic, partially solid tumor, Type III is a completely solid tumor. Treatment of children with PPB is at the discretion of the treating institution. This study builds off of the 2009 study and will also seek to enroll individuals with DICER1-associated conditions, some of whom may present only with the DICER1 gene mutation, which will help the Registry understand how these tumors and conditions develop, their clinical course and the most effective treatments.

NCT ID: NCT03354416 Recruiting - Prostate Cancer Clinical Trials

Profiling of Radiological Factors in Treatment and Outcomes in Prostate Cancer

Start date: February 26, 2018
Phase:
Study type: Observational

Background: Prostate cancer is one of the most common cancers for men in the U.S. There are some new ways to take pictures of the cancer. There are also new ways to use image-guided biopsy and therapy. These could help manage prostate cancer. Researchers want to study how imaging can provide a profile of prostate cancer. They want to collect data to make diagnosis and treatments better. Objectives: To gather data about the radiological and clinical course of prostate cancer. To study imaging-based biomarkers of prostate cancer. Eligibility: Men ages 18 and older with diagnosed or suspected prostate cancer Design: Participants will give permission for researchers to use their medical history and records. Their data will be reviewed, collected, and analyzed. These include results of their tests and scans. Sponsoring Institution: National Cancer Institute

NCT ID: NCT03338985 Recruiting - Clinical trials for Endometrial Hyperplasia and Endometrial Cancers

Role of Senescence in the Development of Endometrial Cancer

Start date: October 16, 2017
Phase: N/A
Study type: Interventional

Several molecular studies showed chromosomal alterations in patients with endometrial cancer, with gains in 1q, 19p, 19q, 8q, 10q and 10p and loss of 4q, 16q and 18q. Several genes of interest have been identified (P53, PTEN, PIK3CA, ß-catenin, K-ras ...). A study has already been carried out at the Reims University Hospital with inclusion of patients with endometrial cancer and patients with endometrial hyperplasia. It identified specific alterations of nosologic continuum of pathology and characterize areas of interest on the genome.