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NCT ID: NCT02646969 Completed - Clinical trials for Healthy Term Infants

Growth and Metabolic Biomarkers of Healthy Term Infants Fed Formulas With Staged Protein Concentrations Over the First Year of Life

Start date: October 2015
Phase: N/A
Study type: Interventional

Growth and metabolic biomarkers of healthy term infants fed formulas with staged protein concentrations over the first year of life

NCT ID: NCT02646592 Completed - Pain Clinical Trials

Effect of a Bolus of 10 µg/kg of Alfentanil on the Pupillary Pain Index

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

This study aims to assess the Pupillary Pain Index before and after a bolus of alfentanil in children under general anesthesia, before skin incision.

NCT ID: NCT02646566 Completed - Clinical trials for Postoperative Nausea and Vomiting

Study of APD421 as PONV Treatment (Prior Prophylaxis)

Start date: March 2016
Phase: Phase 3
Study type: Interventional

Double-blind, randomised, parallel-group, placebo-controlled, adaptive, seamless, dose-selecting study to compare the efficacy of APD421 to placebo as treatment of established PONV, in patients who have had prior PONV prophylaxis.

NCT ID: NCT02643992 Completed - Clinical trials for Per-procedural Concentrations of Oral Anticoagulants

Per-procedural Concentration of Direct Oral Anticoagulants

CORIDA
Start date: June 2013
Phase: N/A
Study type: Observational

Background: Peri-procedural management of direct oral anticoagulants (DOAC) is challenging. The optimal duration of pre-procedural discontinuation that guarantees a minimal DOAC concentration ([DOAC]) at surgery is unknown. The usual 48-hour discontinuation might not be sufficient for all patients. Objectives: To investigate the factors associated with per-procedural [DOAC]. To test the hypothesis that a 48-hour DOAC discontinuation is not sufficient to ensure a minimal perprocedural [DOAC], defined as [DOAC] < 30 ng/mL. Methods: Patients treated with DOAC, and requiring any invasive procedure will be included in this multicentre, prospective, observational study. [DOAC], will be measured during invasive procedure.

NCT ID: NCT02643550 Completed - Clinical trials for Head and Neck Neoplasms

Study of Monalizumab and Cetuximab in Patients With Recurrent or Metastatic Squamous Cell Carcinoma of the Head and Neck

Start date: December 2015
Phase: Phase 1/Phase 2
Study type: Interventional

The objective of this study is to evaluate in a 3 +3 design, the safety of escalating doses of Monalizumab given IV in combination with cetuximab in patients who have received prior systemic regimen(s) for recurrent and/or metastatic squamous cell carcinoma of the head and neck (SCCHN). Cohorts expansion will evaluate antitumor activity of monalizumab and cetuximab with or without anti-PD(L)1

NCT ID: NCT02642926 Completed - Menorrhagia Clinical Trials

Comparison of the Efficiency of Bipolar Energy Versus Monopolar Energy in Endometrial Ablation in Women Having Menorrhagia

Start date: December 2012
Phase: N/A
Study type: Interventional

Since the development a few years ago of bipolar energy in the surgery by operative hysteroscopy, the hysteroscopic treatment of menorrhagia by endometrial ablation can be achieved either by the use of monopolar or bipolar current, in parallel with other techniques labelled as 'second generation' (microwave, radio frequency, thermal destruction ...) treating the uterine cavity. It seems that the use of the bipolar energy decreases the rate of adhesions but prospective data on the success rate after bipolar endometrial ablation are poor and there is currently no recommendation as to the choice of technique to use. No prospective assessment exists to date in the literature to compare the difference in efficacy on bleedings when using monopolar or bipolar current. The goal of this study is to compare these two energies, by measuring the amount of bleeding calculated by the Higham score 12 months after the intervention.

NCT ID: NCT02641054 Completed - Clinical trials for Idiopathic Parkinson Disease

Efficacy Phase IIa Study of CVXL-0107 in Advanced Parkinson's Disease

Start date: February 2016
Phase: Phase 2
Study type: Interventional

CVXL-0107 a glutamate release inhibitor, has shown evidence of antiparkinsonian and antidyskinetic activity in a macaque model and has shown a significant effect on the UPDRS-III (Movement Disorder Society - Unified Parkinson's Disease Rating Scale) while "ON", as well as an increase of "ON-time" without dyskinesia or without troublesome dyskinesia in a previous phase 2a proof of concept study. This study will confirm the efficacy of CVXL-0107 in combination with optimal dose of levodopa on motor symptoms of Parkinson's disease (PD) .

NCT ID: NCT02640664 Completed - Clinical trials for Retinopathy of Prematurity (ROP)

Rainbow Extension Study

RainbowExt
Start date: June 16, 2016
Phase: Phase 3
Study type: Interventional

The purpose of this study was to evaluate the long term efficacy and safety of intravitreal ranibizumab compared with laser ablation therapy in patients who were treated for retinopathy of prematurity (ROP) in the core study CRFB002H2301 (NCT02375971)

NCT ID: NCT02640365 Completed - Clinical trials for Unresectable Advanced Cancer

A Dose Escalation Study of MM-398 Plus Irinotecan in Patients With Unresectable Advanced Cancer

DOUBLIRI
Start date: November 18, 2015
Phase: Phase 1
Study type: Interventional

MM-398 (also known as PEP02) is nanoliposomal encapsulated irinotecan: the liposomal formulation is designed to extend plasma circulation and to increase accumulation in the tumor through the enhanced permeability and retention (EPR) effect. This study introduces a new concept of combining free and nanoliposomal drugs.

NCT ID: NCT02640287 Completed - Clinical trials for Waldenström Macroglobulinemia

Expression of Ku70/XRCC6 in Waldenström's Macroglobulinemia

WAL-KU
Start date: February 2016
Phase: N/A
Study type: Interventional

Waldenström's macroglobulinemia is a rare disease whose pathophysiology remains at present poorly understood, although a recurrent mutation (L265P MYD88) has recently been described. Unlike other lymphoproliferative disorders, there is a defect in isotype switching, mechanism involving AID and NHEJ complex. Using a two-dimensional electrophoresis technology, our group showed that MW had a specific proteomic profile, and one of the differentially expressed proteins is Ku70 (encoded by XRCC6 belonging to NHEJ complex) . The investigators purpose to explore the mechanisms of underexpression of Ku70/XRCC6 (genetic or epigenetic modification) in comparison with other lymphoid malignancies and normal B cells.