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NCT ID: NCT03888443 Completed - Clinical trials for Unilateral Spastic Cerebral Palsy

"Be an Airplane Pilot": A Bimanual 3D Motion Analysis in Children With Unilateral Cerebral Palsy

BE-API
Start date: February 13, 2019
Phase:
Study type: Observational

Cerebral Palsy, in particular in its unilateral spastic form (uCP), is the main cause of motor disability in children, with a prevalence of 2/1000 births. These children have upper limb motor impairments that hinder the realization of activities of daily life in bimanual situations. 3D motion analysis (3DMA) is an objective and precise tool, considered as the gold standard for gait analysis. The existing 3DMA protocols consist of movements too standardized, in unimanual situations away from gestures of everyday life, or have not been validated in bimanual situations. In a preliminary study, a 3DMA bimanual protocol was study. it was composed of 4 tasks integrated into a game scenario to have more spontaneity of movements, similar to those experienced by children in daily life. It allows the exploration of all degrees of freedom of the upper limb. Results showed an excellent acceptability and within day reliability on 20 uCP children and 20 typically developing children (TDC) for funct

NCT ID: NCT03888391 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder (ADHD)

12 Month Open Extension of TNS for ADHD.

Start date: December 1, 2014
Phase: N/A
Study type: Interventional

Participants who exhibit sufficient ADHD symptom improvement in a prior study of active TNS will be invited to continue in a 12-month extension study, designed to collect additional data on long-term response and tolerability and to provide participants ongoing clinical benefit from treatment.

NCT ID: NCT03888092 Completed - Clinical trials for Esophageal Squamous Cell Carcinoma

Z650 in Advanced Esophageal Squamous Cell Carcinoma With EGFR Over Expression or Gene Amplification

Start date: August 18, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of Z650 in Advanced Esophageal Squamous Cell Carcinoma patients With EGFR Over expression or Gene Amplification.

NCT ID: NCT03888014 Completed - Brain Tumor Clinical Trials

Intraoperative Fluorescence With Augmented Reality

Start date: July 1, 2019
Phase:
Study type: Observational

This is a study looking at a new way to evaluate vascular problems or tumors in brain surgery patients using a standard & approved intravenous dye and augmented reality.

NCT ID: NCT03887910 Completed - Clinical trials for Postpartum Depression

Northwell Health Visits: A Family Connects Pilot Implementation at Northwell Health

Start date: January 9, 2019
Phase: N/A
Study type: Interventional

Northwell Health Visits (NHV) is a three year pilot replication of the evidence-based model, Family Connects, which is a brief universal Nurse Practitioner home visiting program for new mothers and their infants. We seek to compare outcomes among mothers and infants enrolled in the NHV enhanced intervention arm, those enrolled in the NHV screening-only arm, and those in the control arm. NHV will follow a three- armed randomized control trial design.

NCT ID: NCT03887169 Completed - Clinical trials for Pulmonary Alveolar Proteinosis

Administration of Methionine in Patients With Pulmonary Alveolar Proteinosis by Mutation of the MARS Gene.

MetPAP
Start date: September 16, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine the safety and tolerance of an oral administration of methionine in the treatment of pulmonary alveolar proteinosis due to the double mutation Ala393Thr / Ser567Leu in the MARS gene. This disease is very severe and especially leads to chronic respiratory insufficiency. There is no curative treatment for this disease. The MARS gene encodes the methionine tRNA synthetase (MetRS). Mutations in this gene leads to a defect in MetRS function. In cultured mutated yeast, addition of methionine in culture medium restores MetRS function. Therefore, the investigators hypothesized that treatment of patients with methionine could have beneficial effects on the disease.

NCT ID: NCT03886909 Completed - Physical Activity Clinical Trials

Impact of Prehabilitation in Oncology Via Exercise- Bone Marrow Transplant

IMPROVE-BMT
Start date: June 28, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether patients are able to participate in a prehabilitation program (prior to the beginning of treatment) which includes: (1) a home-based exercise program or (2) just a prehabilitation education session.

NCT ID: NCT03886896 Completed - Postoperative Pain Clinical Trials

Intravenous Lidocaine in Children Undergoing Laparoscopic Appendectomy

Start date: March 22, 2019
Phase: Phase 4
Study type: Interventional

Intravenous lidocaine - a potent local anesthetic with analgesic and anti-inflammatory properties has been shown to be an effective adjunct that reduces intra and postoperative opioid consumption and facilitates pain management in adults. In children population promising but limited evidence is available. The study was planned to evaluate the efficacy of continuous intravenous infusion of lidocaine to reduce opioid consumption during and after laparoscopic appendectomy in children.

NCT ID: NCT03886831 Completed - Clinical trials for Adenoid Cystic Carcinoma

A Study of PRT543 in Participants With Advanced Solid Tumors and Hematologic Malignancies

Start date: February 11, 2019
Phase: Phase 1
Study type: Interventional

This is a Phase 1 cohort, dose-escalation, dose-expansion study of PRT543 in patients with advanced cancers who have exhausted available treatment options. The purpose of this study is to define a safe dose and schedule to be used in subsequent development of PRT543.

NCT ID: NCT03886779 Completed - Clinical trials for Treatment of Ocular Inflammation Associated With Cataract Surgery

Study Title: Clinical Outcomes of Prolensa (Bromfenac Ophthalmic Solution) 0.07% QD vs. Ilevro (Nepafenac Ophthalmic Suspension) 0.3% QD With Extra (Pulse) Dose on Day of Surgery for Treatment of Ocular Inflammation Associated With Cataract Surgery in a Randomized, Single Masked Clinical Trial

Start date: October 30, 2013
Phase: Phase 4
Study type: Interventional

Clinical Outcomes of Prolensa (Bromfenac Ophthalmic Solution) 0.07% QD vs. Ilevro (nepafenac Ophthalmic Suspension) 0.3% QD with extra (pulse) dose on day of surgery for Treatment of Ocular Inflammation Associated with Cataract Surgery