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NCT ID: NCT02987023 Completed - Infertility, Female Clinical Trials

Uterus Transplantation From Live Donors With Robotic Assisted Surgery - Gothenburg II

UTX-robot
Start date: November 2016
Phase:
Study type: Observational [Patient Registry]

The study is a follow up of NCT01844362. Uterus transplantation will be performed from live donors to patients with uterine factor infertility. If will be performed before transplantation. Organ procurement from the donor will be performed by robotic assisted laparoscopy. Transplantation will be by laparotomy. Embryo transfer will be done 10-12 months after transplantation. After birth of 1-3 children the uterus will be removed by hysterectomy,

NCT ID: NCT02986503 Completed - Osteosarcoma Clinical Trials

European Study in Bone Sarcoma Patients Over 40 Years

EUROBOSS
Start date: January 2002
Phase: N/A
Study type: Observational

The study is a first step of a process to establish the standard chemotherapy treatment with the aim to improve outcome for patients with these rare tumours. For this reason the study will be non-controlled clinical trial. In this regard, the study aims to determine the feasibility of intensive chemotherapy in this age group, and/or separate efficacy analyses according to the different histologic categories and whether the number of patients recruited by the co-operating groups permits future randomised studies.

NCT ID: NCT02985073 Completed - Breast Cancer Clinical Trials

A Comparison Between Biological (Veritas®) vs Non Biological Mesh (TIGR®) in Immediate Breast Reconstruction

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

This study compares the outcome using a biological mesh (Veritas®) compared to a non biological mesh (TIGR®) in immediate breast reconstruction.

NCT ID: NCT02985047 Completed - Suicidal Ideation Clinical Trials

Brief Admission Skane: Replacing General Admission for Individuals With Self-harm and Acute Risk of Suicide

BAS
Start date: September 1, 2015
Phase: N/A
Study type: Interventional

The purpose of the study is to test a standardized version of brief admission (BA) through randomized controlled trial (RCT). The main objective is to evaluate if BA can serve as a crisis management model for individuals with recurrent self-harm, including suicide attempts and at least three symptoms of Borderline Personality disorder. Participants will be allocated to BA + Treatment as Usual (TAU) or TAU.

NCT ID: NCT02984670 Completed - Clinical trials for Sleep Initiation and Maintenance Disorders

Cognitive Behavior Therapy for Insomnia: Analysis of Components, Mediators and Moderators

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

The overall purpose with this investigation is to further our knowledge about cognitive behavioral therapy (CBT) for insomnia by examining treatment components, mediators, and moderators. The first aim that will be addressed is to explore the efficacy of the CBT components with a dismantling-treatment strategy. Two active CBT interventions, intended to define its components - cognitive therapy and behavior therapy - will be compared with one another as well as with a waitlist condition on a broad range of outcomes at five to nine assessment points depending on the measures. The design will thus enable us to examine what CBT component or components are necessary, sufficient and facilitative of therapeutic change. The second aim that will be explored is to investigate what processes occur in CBT that may contribute to treatment outcome with a treatment-mediator strategy. To examine mediators for CBT, the following mediators will be assessed; Anxiety and Preoccupation about sleep Questionnaire (APSQ), Dysfunctional Beliefs and Attitudes about Sleep (DBAS), Sleep Associated Monitoring Index (SAMI), Sleep-Related Behavior Questionnaire (SRBQ), time in bed, napping, bedtime variability, and rise time variability. The hypothesis is that cognitive processes will mediate cognitive therapy outcomes, and that behavioral factors will have a mediating role for behavior therapy improvements. The third aim that will be addressed is to examine what patient characteristics does CBT depend on to be effective with a treatment-moderator strategy. To investigate moderators for CBT, the following moderators will be assessed; age, gender, occupational status, level of education, initial insomnia severity, dysfunction, medication use, chronic pain, psychiatric co-morbidity, medical co-morbidity, behavioral and cognitive processes used as mediators will also be employed as moderators.

NCT ID: NCT02984514 Completed - Type1diabetes Clinical Trials

Brown Adipose Tissue in Type 1 Diabetes

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

Brown adipose tissue has the capacity to consume large amounts of energy and has insulin-independent glucose uptake. The investigators have recently observed an inverse correlation between irisin levels and insulin needs of type 1 diabetes patients. Transplantation of brown adipose tissue to insulin-deficient rats normalized their blood glucose levels. In this study 12 patients with long-standing type 1 diabetes (>10 years) and with variable exogenous insulin needs will be investigated for amount of brown adipose tissue with positron emission tomography using the tracer 18F-deoxy glucose.

NCT ID: NCT02983136 Completed - Clinical trials for Surgical Wound Infection

Safe Hands at the Sharp End- Implementing Aseptic Technique in the Operating Room

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

The aim of this integrated Knowledge Translation (iKT) study is to develop and test a multifaceted implementation intervention for feasibility, acceptability and effectiveness. The intervention will be tailored to fit the context of the operating room (OR), to promote OR team members' use of aseptic techniques during the care of frail persons undergoing acute fracture surgery of the hip. Through the use of an iKT approach, the investigators hypothesise that building on leadership support, partnership between researchers, managers/clinical leaders and healthcare professionals, a solid foundation for the sustained implementation of patient safety innovations can be created.

NCT ID: NCT02982109 Completed - Pain, Postoperative Clinical Trials

Pain Evaluation of Venous Cannulation to Predict Postoperative Pain

Start date: February 27, 2017
Phase:
Study type: Observational

The investigators have recently reported a relationship between pain induced by peripheral venous cannulation and postoperative pain. The purpose of this study is to validate this method of postoperative pain prediction in a larger cohort subjected to different types of surgery.

NCT ID: NCT02979808 Completed - Neurogenic Bowel Clinical Trials

An Open, Qualitative, Prospective, Multicenter Trial of a Novel Transanal Irrigation System in Spinal Cord Injured Patients.

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

This study is designed as an open, prospective, non-controlled, qualitative, multicentre study of a novel transanal irrigation system performed in a population of 150 subjects suffering from spinal cord injury and confirmed neurological bowel dysfunction. The study is expected to last for a total of 1 year (treatment period) with a planned 12- month recruitment period and three scheduled site visits.

NCT ID: NCT02979158 Completed - Clinical trials for Cardiopulmonary Bypass

Preoperative Dual Antiplatelet Therapy: Platelet Function and Influence of Cardiopulmonary Bypass

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

Patients admitted for coronary artery bypass surgery taking antiplatelet medicine have an increased risk for bleeding. Present study aims to compare the platelet function in two patient groups using different types of heart-lung machine methods. It is assumed that one of the methods is superior verified by sensitive methods of testing platelet function.