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NCT ID: NCT00992966 Suspended - Pneumonia Clinical Trials

Vibration Response Imaging (VRI) in Children With Acute Respiratory Symptoms

Start date: n/a
Phase: N/A
Study type: Observational

The VRI device may provide a complementary diagnostic tool for lung examination and aid the physician in determining whether a chest x-ray should be performed.

NCT ID: NCT01114061 Suspended - Diabetes Clinical Trials

Evaluation of the Effects of Heating the Vicinity of the Insulin Delivery Site by the InsuPatch Device During Daily Life

Start date: n/a
Phase: N/A
Study type: Interventional

The aim of this study is to test the performance of the InsuPatch device in daily life. The primary target of the study is to evaluate safety aspect of daily device use. Additional aspects to be evaluated in the study are: the effect of the device on post prandial glucose level.

NCT ID: NCT01222013 Suspended - Clinical trials for Acute Lymphoblastic Leukemia (ALL) Philadelphia Chromosome-positive (Ph+)

Study for Safety and Efficacy Evaluation of Imatinib Mesylate in Children With Acute Lymphoblastic Leukemia (ALL) Philadelphia Chromosome-positive (Ph+)

Start date: n/a
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy, through molecular response and event-free survival, about the use of Imatinib in conjunction with chemotherapy after BFM "like" Induction in children with ALL Ph+.

NCT ID: NCT01477866 Suspended - Colonic Neoplasms Clinical Trials

Utility Of Citogenex Administration In Patients With Colon-Rectal Cancer

CITOGENEX PA
Start date: n/a
Phase: N/A
Study type: Interventional

The main aim of the present study is to test the efficacy and safety of CITOGENEX administration in patients with colon-rectal cancer.

NCT ID: NCT02465008 Suspended - Pain Clinical Trials

Analgesic Effect of Levobupivacaine in Breast Augmentation

Start date: n/a
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether levobupivacaine is effective in the acute postoperative pain treatment in periprosthetic breast augmentation

NCT ID: NCT03051451 Suspended - Clinical trials for Overweight and Obesity

Fixed Dose Combination of Fluoxetin and Metformin in the Management of Overweight and Obesity

Metfluo
Start date: n/a
Phase: Phase 2
Study type: Interventional

Clinical trial, multicenter, double-blind, placebo-controlled, comparative of three parallel groups, randomized treatment to assess the efficacy and safety using a fixed dose combination of metformin hydrochloride with fluoxetine as adjunctive treatment in patient with obesity or overweight in order to generate new knowledge and give a greater number of therapeutic options to the clinicians, one group will receive metformin 1700 mg and 40 mg of fluoxetine; Another group will receive metformin 1000 mg with 40 mg of fluoxetine, and a third group called control will receive placebo. The above described treatments will be administered according to the "Dosage Schedule" The three groups will receive tablets of physical characteristics equal to the reference drug to preserve the blinding.

NCT ID: NCT02778997 Suspended - Clinical trials for Shunt; Complications, Ventricular (Communicating)

Prospective Shunt Complication Study

ShuCS
Start date: April 1, 2017
Phase:
Study type: Observational

Complications in patients with cerebrospinal fluid (CSF) shunts are common. Thus, these patients are frequently admitted for suspicion of a shunt dysfunction (SD). However, the symptoms of a SD are often unspecific and the required diagnostics are time consuming, expensive, invasive and may involve radiation exposure. In a prospective observational study it is planned to find out, how often a suspected shunt dysfunction is found, which kinds of shunt dysfunction are seen and if there is a correlation between the shunt dysfunctions and the age of the shunt. Furthermore, it is intended to find out, if there are symptom-patterns specific for certain shunt dysfunctions.

NCT ID: NCT03275298 Suspended - Ovarian Cancer Clinical Trials

Evolution of the Therapeutic Care in Ovarian Cancer From 2011

ESME-OVR
Start date: April 1, 2017
Phase:
Study type: Observational

The ESME OVR Data Platform is a multi-center real life database using a retrospective data collection process in 18 French Comprehensive Cancer Center (FCCC) over 20 sites). This database compiles data from Patient's Electronic medical records (EMR), inpatient Hospitalisation records and Pharmacy records.

NCT ID: NCT03435172 Suspended - Thermal Burn Clinical Trials

Safety and Feasibility of ADRCs Treatment To Patients With Thermal Wounds

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

The primary objective of the protocol is to evaluate preliminary safety and feasibility of ADRCs via intravenous delivery in the treatment of deep partial and full thickness thermal wounds.

NCT ID: NCT03302650 Suspended - Septic Shock Clinical Trials

Angiotensin II for Septic Shock Treatment

Start date: April 1, 2019
Phase: Phase 3
Study type: Interventional

This study aims to investigate the effect of angiotensin II on microcirculation and peripheral perfusion in patients with septic shock.