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NCT ID: NCT03473340 Terminated - Clinical trials for Disorder Related to Lung Transplantation

Studying the Treatment Effect of Pirfenidone in Chronic Lung Allograft Dysfunction (STOP-CLAD)

Start date: April 27, 2018
Phase: Phase 2
Study type: Interventional

Greater than 50% of lung transplant recipients show signs of chronic lung allograft dysfunction (CLAD) by 5 years post-transplantation.Therapies to prevent or slow CLAD are lacking. Anti-fibrotic therapies may offer an avenue to prevent progression of CLAD and prolong allograft survival. This study investigates if Pirfenidone therapy will stabilize lung function decline and slow progression of Functional small airways disease (fSAD) in lung transplant recipients with CLAD.

NCT ID: NCT03471559 Terminated - Clinical trials for Pharmacokinetics, Bioavailability

Cannabidiol - an in Vivo Innovative Drug Delivery Study

Start date: December 10, 2018
Phase: Phase 1
Study type: Interventional

Basic characterization of the drug delivery system for cannabidiol. A comparative bioavailability study.

NCT ID: NCT03467217 Terminated - Clinical trials for NAFLD - Nonalcoholic Fatty Liver Disease

Losartan for the Treatment of Pediatric NAFLD

STOP-NAFLD
Start date: October 2, 2018
Phase: Phase 2
Study type: Interventional

A multicenter, randomized, double masked, placebo-controlled, parallel treatment groups phase 2 trial of losartan for pediatric nonalcoholic fatty liver disease (NAFLD).

NCT ID: NCT03466801 Terminated - Clinical trials for Idiopathic Membranous Nephropathy

The Efficacy of Prednisone and Combination Therapy With Methylprednisolone and Cyclophosphamide on IMN in Stage I.

Start date: March 20, 2018
Phase: N/A
Study type: Interventional

Multi-center, prospective, randomized, controlled study to verify the efficacy of prednisone alone and combination therapy with methylprednisolone and cyclophosphamide in the treatment of stage I membranous nephropathy.

NCT ID: NCT03466658 Terminated - Clinical trials for Shoulder Arthropathy Associated With Other Conditions

Preoperative Jumpstart for Decolonization of P. Acnes

Start date: November 1, 2018
Phase: N/A
Study type: Interventional

The objective of the study is to evaluate the efficacy of preoperative treatment with a novel, wireless, low-level microcurrent-generating antimicrobial device (brand name: JumpStart) in preventing the spread of Propionibacterium acnes in patients receiving open or arthroscopic shoulder surgery.

NCT ID: NCT03465709 Terminated - Clinical trials for Neovascular Age-related Macular Degeneration

Pegcetacoplan (APL-2) in Neovascular AMD

Start date: February 14, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

Safety Assessment of Pegcetacoplan in Patients with Neovascular AMD

NCT ID: NCT03463902 Terminated - Clinical trials for Schizophrenia and Related Disorders

Transcranial Direct Current Stimulation (tDCS) to Improve Gesture Control

GesttDCS
Start date: January 29, 2018
Phase: N/A
Study type: Interventional

The majority of schizophrenia patients is impaired in hand gesture performance, which contributes to poor functional outcome and poor communication skills. The left inferior frontal gyrus (IFG) and the left inferior parietal lobe (IPL) are key nodes of the gesture network, which is less active in patients with schizophrenia. Here, the investigators test single 10 min sessions of tDCS known to either enhance or inhibit local brain activity for app. 1 hour. The investigators aim to determine, which protocol may improve gesture performance in patients and healthy controls. This is a randomized, double-blind, cross-over, placebo-controlled single-center trial in 20 patients with schizophrenia spectrum disorders and 20 healthy controls. Gesture performance will be tested immediately after each tDCS session, which are separated by 24 hours. Results of this study will inform larger interventional trials comparing 2 tDCS protocols with repeated administration.

NCT ID: NCT03463161 Terminated - Clinical trials for Head and Neck Cancer

Epacadostat and Pembrolizumab in Patients With Head and Neck Cancer That Have Failed Prior Immunotherapy

ORKA
Start date: March 23, 2018
Phase: Phase 2
Study type: Interventional

Study to determine response rate of the combination of pembrolizumab plus epacadostat in patients with head and neck cancers that have received prior immunotherapy.

NCT ID: NCT03462563 Terminated - Clinical trials for Subjects Scheduled to Undergo Laparoscopic Radical Resection of Rectal Carcinoma With Preventive Ileostomy

Prospective, Multicenter, Randomized Controlled Study to Evaluate the Effect of INTERCEED™

Start date: April 16, 2018
Phase: Phase 3
Study type: Interventional

This is a prospective, randomized controlled study. The study population will include 220 subjects scheduled to undergo laparoscopic radical resection of rectal carcinoma with preventive ileostomy (Phase 1 operation). During the Phase 1 operation, when the definite decision to create a temporary ostomy is made, patients will be randomized in 1:1 ratio to either the treatment arm (INTERCEED™) or the control arm (standard of care treatment: no adhesion barrier, no placebo). In subjects assigned to the treatment arm, the INTERCEED™ must be applied beneath the target incision site (the midline incision mainly for the removal specimen). The subjects will return 3-9 months after the phase 1 operation (colorectal resection with temporary ileostomy) for phase 2 operation, to have their diverting ostomy taken down (ileostomy reversal). During the phase 2 operation (ileostomy reversal), the incidence, extent and severity of adhesions will be evaluated through the laparoscope.

NCT ID: NCT03460704 Terminated - Clinical trials for Non Cystic Fibrosis Bronchiectasis

Trial in Non-cystic Fibrosis Bronchiectasis Patients With Chronic Lung Infections Treated With Colistimethate Sodium.

PROMIS-II
Start date: January 29, 2018
Phase: Phase 3
Study type: Interventional

The primary objective of the trial was to investigate the effect of the use of inhaled colistimethate sodium (CMS), administered twice a day (b.i.d.) via a specific nebulizer for 12 months, compared to placebo in subjects with non-cystic fibrosis bronchiectasis (NCFB) chronically infected with P. aeruginosa on the annualised frequency of pulmonary exacerbations.