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NCT ID: NCT06269497 Completed - Clinical trials for Alveolar Bone Resorption

TiO2-scaffolds for Alveolar Ridge Preservation

TIOSCAFF
Start date: November 9, 2021
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to evaluate the safety of placing TiO2 scaffolds in alveolar ridge and to evaluate if the scaffold material contributes to maintain the anatomy and the volume of the alveolar process after tooth extraction.

NCT ID: NCT06200246 Completed - Clinical trials for Heart Failure, Left-sided

Cardio-vascular Energy Transfer and Ventriculo-arterial Coupling in Heart Failure

Start date: October 1, 2022
Phase:
Study type: Observational

The goal of this pilot study is to investigate energy transfer fram the ventricle to the arteries in patients with heart failure, primary by investigating the total power.

NCT ID: NCT06157112 Completed - Clinical trials for Musculoskeletal Pain

Students' Lifestyle Behaviour and Later Health Care Utilization Due to Musculoskeletal Pain

Start date: February 6, 2018
Phase:
Study type: Observational [Patient Registry]

This study aims to assess whether there is an association between students' lifestyle behaviour, in terms of physical activity level, sleep duration, smoking status, alcohol consumption and use of cannabis and other illegal drugs, and later health care utilisation due to musculoskeletal pain. The study will combine data from a national survey in Norway (SHOT2018), in which all full-time university students in Norway were invited, with data from a register on health care utilisation in primary health care.

NCT ID: NCT06093074 Completed - Clinical trials for Spinal Cord Injuries

Self-management Program for Patients in the Sub-acute Phase After Traumatic Injury - a Feasibility Study

SMS_trauma
Start date: October 16, 2023
Phase: N/A
Study type: Interventional

The goal of this descriptive non-randomized feasibility study is to assess aspects of feasibility of the intervention arm in a planned full-scale randomized controlled trial testing the effectiveness of a self-management program for persons who have sustained a moderate to severe traumatic injury. All outcomes will be evaluated based on pre-defined success criteria. The main outcomes in the feasibility study are: - Consent rate of eligible patients - Drop-out rate - Attendance rate in the program sessions Secondary outcomes are the participants' acceptance, reception, and perceived usefulness. Other outcomes are fidelity and protocol adherence, as well as the feasibility of a telehealth version of the program and the data collection methods. The participants will receive a group-based self-management program consisting of eight weekly 2.5-hour sessions delivered by a multidisciplinary team. The self-management program is manualized and includes psychoeducation, training in self-management skills and strategies, setting goals, action planning, and sharing of experiences. The participants will also complete the pre- and post-intervention assessments.

NCT ID: NCT06083272 Completed - Respiratory Failure Clinical Trials

VitalThings Guardian Contactless Monitoring

VINCENT
Start date: November 15, 2023
Phase:
Study type: Observational

This is a confirmatory study without any intervention. It is an uncontrolled, non-randomized and open-label study with measurements made with comparators, and it has a preset hypothesis for the primary endpoint. There are no similar devices to VitalThings Guardian M10 / M10 mobile on the market, consequently one or more different types of devices must be used as comparators.

NCT ID: NCT06033755 Completed - Clinical trials for Exercise Induced Laryngeal Obstruction (EILO)

Managing Dysfunctional Breathing and Exercise-induced Laryngeal Obstruction in Adolescent Athletes

Start date: December 10, 2018
Phase: N/A
Study type: Interventional

This study aimed to assess if a multidimensional individually tailored intervention, including Norwegian Psychomotor Physiotherapy (NPMP), elements of cognitive behavioural therapy and a rehabilitation plan, helped reduce inspiratory distress and dysfunctional breathing in adolescent athletes with EILO. A mixed methods design, which combined qualitative and quantitative research, was used. Data, including subjective experiences of respiratory distress, findings from NPMP body examinations and objective measurements of lung function and aerobic capacity were gathered before and after a five month intervention involving 18 participants.

NCT ID: NCT06003205 Completed - Edema Clinical Trials

Contributing Factors to Local Bioimpedance Spectroscopy

COBI
Start date: September 4, 2023
Phase: N/A
Study type: Interventional

This is an exploratory interventional study. The aim of the investigation is to identify and quantify contributing factors to local bioimpedance spectroscopy (BIS) measured by a wearable sensor patch, particularly the effect of fluid shifts caused by postural changes and lower body negative pressure (LBNP).

NCT ID: NCT05996757 Completed - Emergencies Clinical Trials

Effect of Wet Clothing Removal Compared to Use of a Vapor Barrier in Accidental Hypothermia

Start date: March 20, 2017
Phase: N/A
Study type: Interventional

The optimal method of prehospital insulation and rewarming of hypothermic patients have been subject of debate, and there is a substantial lack og high-quality evidence to guide providers. One question concerns whether or not the patients clothing should be removed prior to being wrapped in an insulating model with a vapor barrier. Evaporative heat loss is one of four mechanisms of heat loss, and preventing evaporative heat loss should be a prioritized task for providers. Removal of wet clothing usually means subjecting the patient to the environment, but will reduce the evaporative heat loss considerably. An other alternative is to encapsulate the patient in a vapor barrier. Evaporative heat loss will stop when the humidity inside the vapor barrier reaches 100%. We aim to investigate whether it is recommended to removed wet clothing or encase the patient in a vapor barrier.

NCT ID: NCT05993468 Completed - Clinical trials for Complex Post-Traumatic Stress Disorder

A Pilot Study of a Trauma-Sensitive Mindfulness and Compassion Intervention

Start date: January 1, 2019
Phase:
Study type: Observational

This mixed-methods pilot study aim to assess the changes in symptoms of post-traumatic stress disorder (PTSD), complex post-traumatic stress disorder (CPTSD), dissociative symptoms, self-critique, and self-compassion following participation in a 16-week trauma-sensitive mindfulness and compassion (TMC) intervention. Adverse experiences of participation are also explored explicitly.

NCT ID: NCT05940727 Completed - Iodine Toxicity Clinical Trials

Macroalgae Consumption - a Pilot Study

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

In this study, the aim is to investigate the food safety of macroalgae. There will be an analysis of macroalgae products for the concentration of cadmium, inorganic arsenic, and iodine in macroalgae, as well as measure the status of these elements in consumers. An investigation of the thyroid function of macroalgae consumers and the use of metabolomics to explore which biological changes occur when consuming seaweed and kelp and when the consumer excludes macroalgae from their diet will be performed.