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Trauma clinical trials

View clinical trials related to Trauma.

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NCT ID: NCT03751189 Completed - Trauma Clinical Trials

Role of Overjet and Trauma in Libyan Children

Start date: May 10, 2016
Phase:
Study type: Observational

Traumatic dental injuries are one of the commonly encountered dental emergencies. Missing anterior tooth in children due to any injury can be a source of considerable physical and psychological discomfort for the child. These consequences also have significant impact on parents, who are generally concerned with esthetic and economic aspects of this problem. It varies from small crack in the enamel to complete loss of the tooth. Injury to children teeth can be both painful and traumatic to the children

NCT ID: NCT03664063 Completed - Trauma Clinical Trials

PK PD Study of IDA and Azithromycin for NTDs ( ComboNTDs )

Start date: September 1, 2018
Phase: Phase 2
Study type: Interventional

This is a Pharmacokinetic and Pharmacodynamic study evaluating the safety of co-administering Azithromycin alongside the new IDA (Ivermectin, Diethylcarbamazine, Albendazole) combination treatment for LF. Individuals will be randomised to receive Azithromycin alone, IDA or combination therapy. Clinical and biochemical monitoring for safety will be undertaken. Drug levels will be measured in each of the three arms to assess whether combination therapy significantly alters drug levels.

NCT ID: NCT03658278 Completed - Trauma Clinical Trials

Trauma Screening and Supplementation

Start date: March 15, 2018
Phase: N/A
Study type: Interventional

The purpose of the proposed study is twofold: 1) The investigators will evaluate ultrasound imaging to screen trauma patients to identify patients at increased risk of postoperative complications associated with sarcopenia. 2) The investigators will evaluate a commercially-available oral nutritional supplement that has previously been evaluated in critically-ill intensive care patients and shown benefit for decreasing complications including decreased wound healing complications, decreased pressure ulcers, decreased skeletal muscle loss due to immobilization, and decreased one-year mortality.

NCT ID: NCT03581461 Completed - Trauma Clinical Trials

Trauma-Informed Mindfulness-Based Yoga

TIMBY
Start date: January 14, 2019
Phase: N/A
Study type: Interventional

The proposed study aims to gather the multiple types of preliminary data needed to design a large and rigorous pragmatic, cluster randomized trial on the impact of a trauma-informed mindfulness-based yoga program on enhancing self-regulation (in the short-term) and reducing recidivism (in the long-term) among juvenile justice-involved youth. Such a study will ultimately provide more definitive outcomes related to the effectiveness of these programs this population. If effective, the assimilation of such programs into the treatment plans of youth in juvenile justice facilities and in other residential settings could have a significant impact on a range of health, educational, vocational, and interpersonal outcomes relevant to this population.

NCT ID: NCT03571737 Completed - Trauma Clinical Trials

Efficacy of Lidocaine Patch in Acute Musculoskeletal Pain in the Emergency Department

Start date: June 23, 2018
Phase: Phase 3
Study type: Interventional

This study evaluates the addition of a lidocaine patch to ibuprofen in the treatment of acute musculoskeletal pains. Half of the participants will get only ibuprofen for their pain, while other half will receive lidocaine patch plus the ibuprofen. After addition of the pain medications, the participants will be followed for their pain scores and return visits.

NCT ID: NCT03557073 Completed - Trauma Clinical Trials

The Effects of Postoperative Physician Phone Calls for Hand and Wrist Fractures

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

This study seeks to determine if postoperative phone calls by a physician affect outcomes in hand surgery.

NCT ID: NCT03515564 Completed - Depression Clinical Trials

Arts and Movement Therapies for Trauma

Start date: July 26, 2017
Phase: N/A
Study type: Interventional

The current goal of this project is to subjectively and objectively assess the efficacy of arts and movement interventions--including dance/movement therapy, art therapy and mindful yoga for youth and adults exposed to trauma, including families resettled as refugees and families in high-risk, low-resource environments. The overarching aim is to measure the changes over time in self-reported symptoms of posttraumatic stress disorder, anxiety disorder(s), depression, and somatic symptoms, as well as changes in biological substrates representing pathophysiological processes involved in responses to stress, trauma, and the aforementioned disorders. These biological substrates include inflammatory proteins and the stress hormone cortisol. We hypothesize that given the emotional and physical components of arts and movement therapies, which are implemented in group settings and confer life-long coping skills to participants, participation in arts and movement therapies will result in reduction of self-reported severity of psyciatric symptoms and improved physiology. COVID-19: In March, the COVID-19 pandemic caused in person research to be halted in order to be in adherence to the stay at home order for the State of Michigan. The IRB overseeing the present project approved an amendment to allow data to be collected online via phone or email, based on participant preference, with a new consent form for this new method of data collection. Following this approval, we migrated our programming to virtual formats and began to serve both refugee commuities as well as school-aged youth with the intervention program and obtained consent followed by data from participants as part of this study. We have pivoted towards also looking at the benefits of creative arts and movement based interventions in reducing COVID-related distress, as well as building resilience. By collecting psychological and biomarker data the investigators seek concrete scientific evidence supporting these non-pharmacological, cost effective, and accessible programs as reliable treatment options.

NCT ID: NCT03512392 Completed - Sepsis Clinical Trials

Role of Active Deresuscitation After Resuscitation-2

RADAR-2
Start date: April 10, 2018
Phase: N/A
Study type: Interventional

RADAR-2 will be a randomised, open-label, allocation concealed, pilot trial of conservative fluid administration and deresuscitation compared with usual care in patients who are critically ill.

NCT ID: NCT03491644 Completed - Trauma Clinical Trials

Restrictive vs. Liberal Oxygen Therapy for Trauma Patients

TRAUMOX
Start date: April 3, 2018
Phase: Phase 4
Study type: Interventional

The objective of this trial is to investigate whether treatment with oxygen in the early phases after a trauma plays a role in recovery.

NCT ID: NCT03485573 Completed - Trauma Clinical Trials

Improvement of Trauma Care Quality by Implement Trauma Register in a Middle Income Country

Start date: May 8, 2018
Phase:
Study type: Observational [Patient Registry]

Every year more people die from traumatic injuries than from infections such as malaria, tuberculosis, and HIV/AIDS. About 3000 people are killed annually on Kenyan roads. Hospital trauma registers have played a key role in the advancement of patient-based research and trauma care. Trauma registers offer a unique opportunity to document patient characteristics and audit outcomes, thereby creating a platform for clinical research. One of these systems is the ICD-based Injury Severity Score (ICISS) derived from and validated on hospital data to predict hospital death. The establishment of the register enables us to compare the trauma care quality with other existing or upcoming trauma registers, in different settings.