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NCT ID: NCT02875704 Terminated - Clinical trials for Diabetic Retinopathy

Oxidative Stress In Stargardt Disease, Age Related Macular Degeneration and Diabetic Retinopathy

Start date: January 3, 2017
Phase:
Study type: Observational

In this study, markers of oxidative stress will be measured in the aqueous humour of stargardt disease, age related macular degeneration and diabetic retinopathy patients compared to controls.

NCT ID: NCT02874105 Terminated - Clinical trials for Subacromial Impingement of the Shoulder

Glenohumeral Re-centering During Closed Kinetic Chain for Shoulder Physiotherapy. A Prospective and Randomized Study.

SCAPULEO
Start date: August 30, 2016
Phase: N/A
Study type: Interventional

The rotator cuff tendinopathy is very common and associated with degenerative or traumatic changes of the rotator cuff and/or the sub-acromial bursa or the long head of the biceps. Lesions go of the simple tendinopathy without tear to the full-thickness tear of the cuff which means a loss of mobility or strength. The origin of this pathology remains controversial and many causes have been evoked (subacromial mechanical impingement, degenerative changes, muscle imbalance…). The clinical impairment is not always the same and varies from a painful shoulder with correct range of motion to a pseudoparalysis shoulder. The first treatment of the rotator cuff pathology is always non surgical and consists in relative resting, painkillers and/or non-steroidal anti-inflammatory drugs (NSAD) and physiotherapy. The aim of this management is to relieve pain and to restore the mobility and a good function of the shoulder. There is no consensus about the physiotherapy protocol for the treatment of the rotator cuff tendinopathy. In France, the most used physiotherapy protocol uses the strengthening of the muscles which stabilize the scapula (rhomboide muscles, trapezius and serratus anterior) and which lower the humerus (pectoralis major, latissimus dorsi and teres major). The aim of this approach is to augment the subacromial space in order to decrease the inflammation of the rotator cuff tendons and the associated pain. A technique of Dynamic Humeral Centering (DHC) uses a new method of glenohumeral centering in closed kinetic chain has been described ("3C Concept" for Centering in a Closed Chain). Dynamic humeral centring (DHC) is a modality of physiotherapy that aims to prevent subacromial impingement of rotator cuff tendons. In order to simplify and to improve its reliability, a special device called Scapuleo® has been developed. The aim of this device is to help the physiotherapist to realize simultaneously a subacromial decompression, a specific strengthening of the rotator cuff muscles and an optimal activation of the lower trapezius and the anterior serratus. Our hypothesis was that the DHC was not inferior to the conventional physiotherapy protocol for the medical treatment of the rotator cuff tendinopathy without full-thickness tear. We proposed a prospective and randomized study. All the patients treated in our department for simple tendinopathy of the rotator cuff or partial thickness tear were included in this study after signed consent. The physiotherapy protocol consists in 20 sessions of either "Conventional program" (Control group) or "Dynamic Humeral Centering" (Study group). The clinical evaluation included the range of motion measurement, Constant Score, Quick-DASH and Oxford Shoulder Score at 3 months and 6 months. Patients were blinded to the study hypothesis. The assessor of all outcomes was blinded to the interventions.

NCT ID: NCT02873624 Terminated - Clinical trials for Acute Kidney Injury ,Laparoscopic Cholecystectomy

Incidence of Acute Kidney Injury After Laparoscopic Cholecystectomy

Start date: September 2016
Phase:
Study type: Observational

The aim of this study is to establish AKI incidence in patients who are undergoing laparoscopic cholecystectomy and to identify the potential risk factors associated with the development of AKI.

NCT ID: NCT02873325 Terminated - Clinical trials for Infectious Complications Following HSCT

Registry on Salvage Antiviral Treatment for Patients Experiencing ADV and / or CMV Reactivation Post Allogeneic HSCT

EPROS
Start date: May 11, 2016
Phase: N/A
Study type: Observational [Patient Registry]

DESIGN: Disease registry - non-interventional. INDICATION: Patients failing first or subsequent line treatment for adenovirus and / or cytomegalovirus reactivation post allogeneic hematopoietic stem cell transplantation.

NCT ID: NCT02872727 Terminated - Clinical trials for Air France Company's Employees Working in the Marseilles and Paris Airports (Flightline and Administrative Employees)

Nanoparticles Emitted by Aircraft Engines, Impact on the Respiratory Function:

NANOAF2
Start date: December 13, 2017
Phase:
Study type: Observational

The object of this new project is to proceed with investigations with the employees of the cohort for the first study so as to obtain a remote evolution (5 years) of their respiratory function while measuring their nanoparticle exposure. This will enable us to assess the possible link between exposure and respiratory function evolution in the employees

NCT ID: NCT02871102 Terminated - Clinical trials for Acute Respiratory Distress Syndrome

Stress Index to Individualize Mechanical Ventilation in ARDS

Start date: August 2016
Phase: N/A
Study type: Interventional

Acute respiratory distress syndrome (ARDS) is a widely prevalent and morbid disease for which the current standard treatment is supportive care and avoidance of complications with lung-protective ventilation. Lower-tidal volume ventilation has been largely accepted as a means of lung protective ventilation, but the mechanism for its effectiveness is not yet clear, and debate remains as to how best to choose positive end-expiratory pressure (PEEP). Reduction in driving pressure (plateau pressure minus PEEP) has been suggested as a possible means to minimize ventilator-induced lung injury. This protocol aims to identify the range of safe paired-settings of PEEP and tidal volume, with selection guided by driving pressure and the stress index, a tool to recognize potential lung hyperinflation during mechanical ventilation.

NCT ID: NCT02868892 Terminated - Clinical trials for Adenocarcinoma of the Cervix

A Study of Pemetrexed in Recurrent Cervical Adenocarcinomas

Start date: July 2015
Phase: Phase 2
Study type: Interventional

Patients with advanced or recurrent adenocarcinoma or adenosquamous cell carcinoma of the cervix will receive Pemetrexed.

NCT ID: NCT02867904 Terminated - Clinical trials for Arthroscopic Shoulder Surgery

Intra-Operative Corticosteroid Injection During Arthroscopic Shoulder Surgery

Start date: March 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the efficacy of intra-operative subacromial corticosteroid injections in patients undergoing arthroscopic shoulder surgery on quality of life scores and activity level when compared to a control group.

NCT ID: NCT02867228 Terminated - Clinical trials for Acute Respiratory Distress Syndrome

Noninvasive Estimation of Work of Breathing

Start date: September 2016
Phase: N/A
Study type: Interventional

This study will evaluate the correlation between invasively measured parameters (work of breathing/power of breathing, resistance and elastance), derived using esophageal pressure measurements, and their corresponding non-invasive estimated values (noninvasive work of breathing/power of breathing, resistance and elastance), computed using airway pressure and flow measurements only.

NCT ID: NCT02866123 Terminated - Intubated Patient Clinical Trials

Verification of Correct Positioning of a Gastric Tube by Ultrasonography

SNG echo
Start date: January 2015
Phase: N/A
Study type: Interventional

There are several ways to verify the correct positioning of a gastric tube. Radiography is considered the reference method. The use of ultrasonography could diminish the number of radiographies necessary. The hypothesis of this research is that gastric ultrasonography performed during insertion of the tube is a reliable examination to check the correct positioning of gastric tubes in intensive care.