Clinical Trials Logo

Filter by:
NCT ID: NCT02937064 Completed - Osteoarthritis Clinical Trials

Multimodal Assessment of Knee Conditions

MAKnee
Start date: November 2016
Phase: N/A
Study type: Observational

The purpose of this study is to assess both osteoarthritis and other pathological knee conditions from the combination of signals that are known to provide information on the knee joint.

NCT ID: NCT02935374 Completed - Acute Otitis Media Clinical Trials

Effect of Antimicrobial Treatment of Acute Otitis Media on the Intestinal Microbiome in Children

AOMMi
Start date: November 2016
Phase: Phase 4
Study type: Interventional

This is a randomized, controlled trial studying the effects of various antimicrobial treatments on the intestinal microbiome of small children. The participating children with acute otitis media are treated wither with amoxicillin, amoxicillin-clavulanate or without antibiotics. The children with allergy to amoxicillin receive a course of macrolide and they will be monitored as a separate group. The main outcomes of this trial are the changes in the intestinal microbiome after the treatment.

NCT ID: NCT02933645 Completed - Insulin Resistance Clinical Trials

Effects of Intranasal Insulin Administration on Tissue Specific Insulin Sensitivity

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

Recent research has suggested that intranasally administered insulin can reach the brain quickly without passing through circulation and evoke increased insulin sensitivity and tissue glucose consumption during insulin stimulation (low-dose hyperinsulinemic, euglycemic clamp). It is still not known what mechanism causes these changes or what tissues are involved in this. In this study, the changes in tissue-specific insulin sensitivity and glucose uptake will be investigated by using glucose-analogue radiotracer ([18F]-fluorodeoxyglucose) with positron emission tomography (PET) imaging during insulin stimulation. Ten healthy males are studied, each receiving nasal sprays containing insulin or placebo in a randomized order on two separate days. After spray administration, glucose uptake in skeletal muscle, liver, subcutaneous and visceral adipose tissue, myocardium, intestines, brown adipose tissue and brain assessed by PET imaging and glucose uptake in these tissues is analyzed. Endogenous glucose production is calculated facilitating the measurements glucose and radiotracer uptake in tissues and tracer loss into urine. As skeletal muscle consumes most of the glucose available, it is likely that administration of insulin sprays will result in an increased uptake in this tissue. Some increase in glucose uptake might also be seen in other tissue types after insulin spray versus placebo spray administration.

NCT ID: NCT02932865 Completed - Infertility, Male Clinical Trials

Modern Analyses of the Semen in Evaluating Male Fertility and Treatment Options of Male Infertility

SemiFluid
Start date: November 2016
Phase:
Study type: Observational

Men are recruited to collect seminal plasma samples and serum samples from men with azoospermia, men receiving medical treatment of infertility and men attending semen analysis. MicroRNA (miRNA) and PiWi-interacting RNA (piRNA) are analyzed for all of the groups to find potential differences. Steroid hormones are analyzed by liquid chromatography-tandem mass spectrometry.

NCT ID: NCT02931721 Completed - Male Infertility Clinical Trials

Treatment of Severe Male Infertility - Predictive Factors (Imaging)

TESE-MRI
Start date: November 1, 2016
Phase:
Study type: Observational

Testes of men with non-obstructive azoospermia (NOA) are imaged using MRI to find potential differences depending on the outcome, ie. sperm recovery in consequent microdissection testicular sperm extraction (MD-TESE).

NCT ID: NCT02931617 Completed - Clinical trials for Postoperative; Dysfunction Following Cardiac Surgery

Comparison of Two Modes of Respiratory Physiotherapy in Cardio-thoracic Surgical Patients

Start date: September 2013
Phase: N/A
Study type: Interventional

Two forms of pre and postoperative physiotherapy are compared in three cohorts of patients undergoing cardio-thoracic surgery: Minor thoracic surgery (biopsy), major thoracic surgery (lobectomy etc, open or VATS) and cardiac surgery

NCT ID: NCT02926989 Completed - Dehydration Clinical Trials

Intravenous Fluids in Hospitalised Children

Start date: October 3, 2016
Phase: Phase 4
Study type: Interventional

The main objective of the trial is to evaluate the risk of hypokalemia following administration of a isotonic solution compared to a hypotonic solution in acutely ill hospitalised children, who need intravenous fluid therapy.

NCT ID: NCT02925117 Completed - Atopic Dermatitis Clinical Trials

A Study to Evaluate ABT-494 (Upadacitinib) in Adults With Moderate to Severe Atopic Dermatitis

Start date: October 25, 2016
Phase: Phase 2
Study type: Interventional

The objective of this study was to evaluate the safety and efficacy of multiple doses of upadacitinib monotherapy versus placebo in the treatment of adults with moderate to severe atopic dermatitis (AD).

NCT ID: NCT02924727 Completed - Clinical trials for Acute Myocardial Infarction

Prospective ARNI vs ACE Inhibitor Trial to DetermIne Superiority in Reducing Heart Failure Events After MI

PARADISE-MI
Start date: December 9, 2016
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of LCZ696 titrated to a target dose of 200 mg twice daily, compared to ramipril titrated to a target dose of 5 mg twice daily.

NCT ID: NCT02919501 Completed - Clinical trials for Depressive Disorder, Major

Study of the Efficacy and Safety of Initial Administration of 17 mg Vortioxetine Intravenously With 10 mg/Day Vortioxetine Orally in Patients With Major Depressive Disorder

Start date: September 27, 2016
Phase: Phase 2
Study type: Interventional

To evaluate the early onset of efficacy of vortioxetine 17 mg intravenously (IV) and vortioxetine 10 mg/day oral dose regimen versus placebo IV and vortioxetine 10 mg/day oral dose regimen on depressive symptoms