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NCT ID: NCT02565121 Completed - Brain Injuries Clinical Trials

Olfaction Disorders in Patients Included in The Trauma Brain Injury (TBI) Database at Trondheim University Hospital

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

The aim of the study is to see whether patients with chronic smell impairment after brain injury benefit from a treatment that consists of corticosteroids, and then olfactory training in 3 months.

NCT ID: NCT02564250 Recruiting - Obesity Clinical Trials

Maternal Metabolism and Pregnancy Outcomes in Obese Pregnant Women

Start date: September 2015
Phase: N/A
Study type: Observational

The purpose of this study is to study longitudinal changes in maternal metabolism and pregnancy outcomes in obese pregnant women.

NCT ID: NCT02563977 Completed - Clinical trials for Breast Reconstruction

Changes To The Abdominal Wall After DIEP Flap Breast Reconstruction

Start date: July 2015
Phase:
Study type: Observational

The purpose of this study was to perform an evaluation of the structural changes in the abdominal wall after harvesting a DIEP flap in breast reconstruction. 14 women undergoing secondary, unilateral breast reconstruction were recruited to the study and underwent a 2 year postoperative CT scan of the abdomen (without contrast). Structural changes were assessed by comparing the abdominal CT scans performed prior to surgery with the 2 year postoperative CT scans.

NCT ID: NCT02563717 Completed - Clinical trials for Infant, Premature, Diseases

Comparison Of Respiratory Support After Delivery on Infants Born Before 28 Weeks Gestational Age

CORSAD
Start date: March 2016
Phase: N/A
Study type: Interventional

Trial purpose: For infants born <28 weeks of age, can initial respiratory resuscitation with new system (low imposed work of breathing and prongs) reduce the frequency of delivery room intubations compared to standard treatment with T-piece resuscitator system (high imposed work of breathing and face mask)? Trial summary: This is a randomised controlled trial of delivery room intubation rates comparing a new system and T-piece resuscitation system for initial stabilisation of infants born <28 weeks.

NCT ID: NCT02563652 Completed - Clinical trials for Systemic Inflammatory Response Syndrome

Can Biomarkers Aid in the Prediction of Postoperative Pain and Circulatory Instability After Major Abdominal Surgery?

Start date: September 2015
Phase:
Study type: Observational

Patients undergoing major surgery are exposed to extensive damage of tissues, which induces widespread activation of the inflammatory system, called 'systemic inflammatory response syndrome' (SIRS).This activation of the inflammatory system may induce instability of the heart and respiration in the postoperative period. The degree of physiologic response to postoperative SIRS as well as the degree of postoperative pain differ between patients. Therefore, patients undergoing anesthesia and major surgery are treated in a 'post anesthesia care unit' (PACU) after end of surgery.Admittance to a PACU is expensive. The time patients need to stay in a PACU after major surgery has not been extensively studied, and more appropriate tools for prediction of length of stay are needed. The main aim of this study is to assess whether clinical observations, inflammatory biomarkers or genetic markers may aid in the prediction of physiological instability and/or pain after major surgery. Such predictors would help clinicians planning the length of PACU-stays.

NCT ID: NCT02562131 Active, not recruiting - Clinical trials for Prostate Cancer Recurrent

PET-MR-PSA Prostate Cancer Recidive Study

PET-MR-PSA
Start date: September 2015
Phase:
Study type: Observational

Simultaneous PET/MRI has the potential to improve the detection accuracy in recurrent prostate cancer, since it combines the excellent soft-tissue contrast of MRI with the high molecular sensitivity of PET in a single imaging session. The aim of this study is to evaluate the sensitivity and specificity of simultaneous 18F-Fluciclovine PET/MRI for detection of recurrent prostate cancer.

NCT ID: NCT02560259 Not yet recruiting - Referred Pain Clinical Trials

The Role of Referred Pain From the Retro Trochanteric Region in Patients With Knee Pain

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

The role of referred pain from the retro trochanteric region, in patients with knee pain. Defining and quantifying this sub group of knee patients in the investigators list of refered knee patients. Evaluating the effect of treatment. A randomized trial.

NCT ID: NCT02558647 Active, not recruiting - Insomnia Clinical Trials

Overcoming Insomnia: Impact on Sleep, Health and Work of Online CBT-I

NORSE-3
Start date: February 2016
Phase: N/A
Study type: Interventional

Insomnia is a major public health concern. While cognitive behavior therapy for insomnia (CBT-I) is acknowledged as the best available intervention, there are unanswered questions about its wider dissemination, socio-economic benefits and its impact on health resource utilization. The aim of this randomized controlled trial (RCT) is to investigate the effectiveness of a fully automated online version of CBT-I compared with online patient education about sleep (PE). Outcome measures comprise changes in symptoms of insomnia, time off work due to sick leave, as well as medication and health resource utilization. Also, we will examine putative mediators and selected potential psycho-bio-social moderators of the effects of the intervention.

NCT ID: NCT02556515 Completed - Clinical trials for Osteoarthrosis of the Carpometacarpal Joint of the Thumb

Joint Replacement or Interpositional Arthroplasty for CMC1 Arthritis, a Prospective Trial

Start date: November 24, 2008
Phase: N/A
Study type: Interventional

Interpositional arthroplasty is by many considered to be the current gold standard for the treatment of thumb carpometacarpal arthritis. The results are generally good, but the rehabilitation time can be long and failures are difficult to treat. Total joint replacements now exist with modern uncemented designs that can be an alternative treatment. Short term studies show that thumb function often is better and rehabilitation time shorter, however there is uncertainty with regards to the longevity of the implants. Currently no prospective randomized trials have compared these two treatment options. Our hypothesis is that the total joint replacement will give the same results or better when compared to the interpositional arthroplasty.

NCT ID: NCT02556203 Terminated - Clinical trials for Transcatheter Aortic Valve Replacement

Global Study Comparing a rivAroxaban-based Antithrombotic Strategy to an antipLatelet-based Strategy After Transcatheter aortIc vaLve rEplacement to Optimize Clinical Outcomes

GALILEO
Start date: December 16, 2015
Phase: Phase 3
Study type: Interventional

To assess whether a rivaroxaban-based anticoagulation strategy, following successful TAVR, compared to an antiplatelet-based strategy, is superior in reducing death or first thromboembolic events (DTE). To assess the primary bleeding events (PBE) of the rivaroxaban-based strategy compared to an antiplatelet-based strategy, following TAVR.