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NCT ID: NCT04252560 Completed - Clinical trials for Colorectal Cancer, Peritoneal Carcinomatosis, Anastomosis Insufficiency

The Impact of Gut Microbiota in Anastomoses Insufficiency After Resection and Direct Anastomosis for Colorectal Cancer.

Start date: January 31, 2020
Phase:
Study type: Observational

The role of gut microbiota in anastomosis insufficiency in patients operated for colorectal cancer and for peritoneal carcinomatosis is going to be investigated. This is a pilot study.

NCT ID: NCT04251455 Completed - Clinical trials for Temporomandibular Joint Disorders

Tissue and Clinical Characterisation of Temporomandibular Joint Diseases

Start date: January 14, 2014
Phase:
Study type: Observational

Temporomandibular joint (TMJ) diseases or dysfunctions affects many patients. Surgical treatment is planned when non-invasive interventions have failed. Still, much is not known regarding aetiology of TMJ diseases and how and why the disease develops over time. The study aims to investigate synovial tissue, synovial fluid and clinical characteristics for patients with TMJ diseases or dysfunctions designated for surgery. Patient samples and clinical variables will be analysed in relation to TMJ diagnosis and related to surgical outcome. The study is a cohort observational study.

NCT ID: NCT04249401 Completed - Atrial Fibrillation Clinical Trials

Study to Gather Information About the Safety of Oral Anticoagulation Drugs and How Well These Drugs Work in Real World for Patients With Non-valvular Atrial Fibrillation (Irregularly Heart Beats Which is Not Caused by a Heart Valve Problem)

REATTAIN
Start date: March 1, 2020
Phase:
Study type: Observational

Oral anticoagulant (OAC) treatment with either vitamin K antagonists (VKAs) or non-vitamin K antagonist oral anticoagulants (NOACs) is essential in patients with atrial fibrillation for the prevention of stroke or systemic embolism (SE) a condition that happens when a blood clot forms elsewhere in the body and travels through the blood stream to plug another vessel. While there are significant number of real-world publications on the use and outcomes of NOACs for stroke prevention, evidence from routine clinical practice on the use and outcomes of reduced doses of NOACs is scarce. By evaluating routine clinical practice data from national registers in Denmark, Finland, Norway and Sweden, researchers want to gather information about the safety and how well reduced doses of NOACs work in patients with irregularly heartbeats which are not caused by a heart valve problem (non-valvular atrial fibrillation, NVAF). As a primary aim of this study, treatment with low doses of NOACs (Xarelto [generic name rivaroxaban], Eliquis [generic name apixaban] or Pradaxa [generic name dabigatran]) will be compared with VKAs (warfarin) in Nordic patients with NVAF to assess the occurrence of stroke and systemic embolism [effectiveness]) and intracranial hemorrhage a type of bleeding that occurs inside the skull [safety]).

NCT ID: NCT04249024 Completed - Peri-Implantitis Clinical Trials

Peri-implantitis, Comparing Treatments 970 nm Laser and Mucosal Flap Surgery

Start date: September 25, 2019
Phase: N/A
Study type: Interventional

A clinical trial comparing laser treatment and conventional mucosal flap surgery for treatment of peri-implantitis. The main aim of the study is to evaluate if treatment of peri-implantitis with 970 nm laser combined with scaling and root planning (SRP) is clinically comparable to conventional mucosal flap surgery in terms of pocket probing depth reduction.

NCT ID: NCT04247009 Completed - Clinical trials for Arthritis, Rheumatoid

Postprandial Inflammation in Rheumatoid Arthritis

PIRA
Start date: February 1, 2020
Phase: N/A
Study type: Interventional

Patients with RA will be studied to see whether meals of different content will affect inflammation and metabolic variables in the postprandial state. Healthy controls will also be invited to examine potentially different responses to patients with RA.

NCT ID: NCT04246736 Completed - Insomnia Clinical Trials

A Proactive Intervention Promoting Strategies for Sleep and Recovery in Nurses

Start date: January 30, 2017
Phase: N/A
Study type: Interventional

Considering the known challenges facing newly graduated nurses, there are possibilities to implement preventive actions. The aim of the current study was to evaluate the effects of a preventive intervention among newly graduated nurses, supporting proactive strategies for sleep and recuperation in relation to work related stress and shift work.

NCT ID: NCT04244890 Completed - Infant, Newborn Clinical Trials

Feasibility of Uninterrupted Infant Respiratory Support Treatment

FUIRST
Start date: February 21, 2020
Phase:
Study type: Observational

Feasibility study of a simplified respiratory support system for newborn infants

NCT ID: NCT04244617 Completed - Mental Disorder Clinical Trials

Peer-supported Internet Mediated Psychological Treatment

Start date: March 1, 2019
Phase: N/A
Study type: Interventional

This study evaluates the effect and experience of peer-support in internet mediated ACT (Acceptance and Commitment therapy) in an explorative pilot study with mixed method design conducted in primary care. Peer-supporters are certified support persons with personal experience of mental health problems and the process of rehabilitation, which becomes professionally active in care and support to patients in their recovery

NCT ID: NCT04241003 Completed - Clinical trials for Spinal Cord Injuries

Effects of the SmartDrive on Mobility, Activity and Shoulder Pain Among People With SCI Using Manual Wheelchairs

Start date: June 11, 2019
Phase: N/A
Study type: Interventional

This is a prospective study of manual wheelchair users with spinal cord injury (SCI). The users will be their own controls. The primary purpose of the study is to evaluate the ability of the power assist device SmartDrive to increase the ability to be mobile.

NCT ID: NCT04240249 Completed - Clinical trials for Problems With Self-assertiveness

Constructive Self Assertiveness Via the Internet

R2
Start date: February 1, 2020
Phase: N/A
Study type: Interventional

Some people have problems with self-assertiveness. That can have negative impact on their lives. This study will test a constructive self-assertiveness intervention program delivered online. In addition, the relative effect of guidance during the intervention will be investigated. In a randomized controlled trial three groups will be compared: 1. constructive self-assertiveness with guidance 2. constructive self-assertiveness without guidance 3. Waitlist control