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Wounds and Injuries clinical trials

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NCT ID: NCT03115970 Not yet recruiting - Trauma, Multiple Clinical Trials

Feasibility of Lactate Level Evaluation in Prehospital Care in Trauma

Start date: May 1, 2017
Phase: N/A
Study type: Observational [Patient Registry]

Capillary or venous lactate level evaluation in prehospital care could be simple and beneficial tool for optimising prehospital care in patients with severe trauma.

NCT ID: NCT03113838 Not yet recruiting - Clinical trials for Drug-Induced Liver Injury

Surveillance for Early Liver Injuries Caused by Yangxue Shengfa Capsule.

Start date: April 17, 2017
Phase: N/A
Study type: Observational [Patient Registry]

This is a prospective registry study to surveil early liver injuries caused by Yangxue Shengfa Capsule (YXSF Capsule) through a non-intervention observational way. And attempt to establish a predictive model to screen susceptibilities to YXSF Capsule.

NCT ID: NCT03110237 Not yet recruiting - Clinical trials for Brain Injuries, Traumatic

A Multidimensional Inpatient Balance Training Class to Improve Functional Outcomes in Rehabilitation Inpatients With ABI

Start date: April 10, 2017
Phase: N/A
Study type: Interventional

Many survivors of acquired brain injury (ABI) suffer from decreased balance and increased risks of falls. Previous studies indicate that balance training improves balance, reduces falls, and increases walking speed and balance confidence. The purpose of this study is to determine if a multidimensional balance training based on the FallProof(TM) approach achieves better improvements in balance and walking performance than the current practice . Participants will be assigned to: 1)a task-oriented circuit training balance class (current practice), or 2) balance training class based on the FallProof(TM) approach. Standardized tests will determine if participating in balance training helps improve balance, walking speed and balance confidence.

NCT ID: NCT03108859 Not yet recruiting - Spinal Cord Injury Clinical Trials

Pre-and In-hospital First Aid Programs and Specifications for Spine and Spinal Cord Injury in Beijing of China

Start date: May 2017
Phase: N/A
Study type: Observational

To establish a spine injury and spinal cord injury (SCI) treatment database; to complete pre- and in-hospital evaluation of spine injury and SCI, develop and optimize first aid procedures, form pre-and in-hospital standardized training program for the treatment of spine injury and SCI; to develop first aid guidelines and establish an evaluation and treatment system for early surgery, as far as possible to save the spinal cord function and reduce the degree of disability; to form expert consensus on acute SCI and "green channel" patterns, will be promoted in hospitals in Beijing and other cities of China, so as to improve the level of first aid treatment of acute spine injury and SCI in Chinese cities, and to reduce the occurrence of secondary injury and severe dysfunction due to improper treatment.

NCT ID: NCT03103516 Not yet recruiting - Clinical trials for Spinal Cord Injuries

Epidural Decompression Surgery Within 24 Hours After Acute Spinal Cord Injury Improves Spinal Nerve Function

Start date: August 2017
Phase: N/A
Study type: Interventional

To compare the effects of early (within 24 hours) and delayed (exceed 24 hours) epidural decompression surgery on the recovery of spinal nerve function in patients with acute spinal cord injury (complete and incomplete) at postoperative 6 months.

NCT ID: NCT03091608 Not yet recruiting - Clinical trials for Drug-Induced Liver Injury

Surveillance for Early Liver Injuries Caused by Xianlin Gubao Granule

Start date: March 25, 2017
Phase: N/A
Study type: Observational [Patient Registry]

This is a prospective registry study to surveil early liver injuries caused by Xianlin Gubao Granule (XLGB Granule) through a non-intervention observational way. And attempt to establish a predictive model to screen susceptibilities to XLGB Granule.

NCT ID: NCT03091556 Not yet recruiting - Clinical trials for Drug-Induced Liver Injury

Surveillance for Early Liver Injuries Caused by Xianlin Gubao Pill.

Start date: March 25, 2017
Phase: N/A
Study type: Observational [Patient Registry]

This is a prospective registry study to surveil early liver injuries caused by Xianlin Gubao Pill (XLGB Pill) through a non-intervention observational way. And attempt to establish a predictive model to screen susceptibilities to XLGB Pill.

NCT ID: NCT03091244 Not yet recruiting - Clinical trials for Drug-Induced Liver Injury

Surveillance for Early Liver Injuries Caused by Xianlin Gubao Capsule.

Start date: March 25, 2017
Phase: N/A
Study type: Observational [Patient Registry]

This is a prospective registry study to surveil early liver injuries caused by Xianlin Gubao Capsule (XLGB Capsule) through a non-intervention observational way. And attempt to establish a predictive model to screen susceptibilities to XLGB Capsule.

NCT ID: NCT03091218 Not yet recruiting - Clinical trials for Drug-Induced Liver Injury

Surveillance for Early Liver Injuries Caused by Runzao Zhiyang Capsule.

Start date: March 25, 2017
Phase: N/A
Study type: Observational [Patient Registry]

This is a prospective registry study to surveil early liver injuries caused by Runzao Zhiyang Capsule (RZZY Capsule) through a non-intervention observational way. And attempt to establish a predictive model to screen susceptibilities to RZZY Capsule.

NCT ID: NCT03086031 Not yet recruiting - Brain Injuries Clinical Trials

Manual-Based Vocational Rehabilitation Program for Patients With Acquired Brain Injury

Start date: August 2017
Phase: N/A
Study type: Interventional

An acquired brain injury (ABI) is a complex injury often followed by a broad range of cognitive, physical, emotional, and behavioral disabilities. Because of these disabilities, vocational rehabilitation (VR) is a challenging task, however, of great importance, since approximately 75% of the patients with ABI are of working age. Thus, standardized clinically effective and cost-effective methodologies regarding VR for patients with ABI are highly needed. This study is an interventional, two-arm, 6-month follow-up, cluster randomized controlled trial involving four municipalities in the Zealand Region and the Capital Region of Denmark. A total of 84 patients with ABI evenly distributed across four municipalities will be included in the study. The patients will randomly be allocated in a 1:1 ratio to the VR intervention provided by a specialized Brain Injury Centre or the conventional VR provided by the municipalities (usual care). The 6-9 month intervention will consist of individual and group therapies as well as a work placement program including supported employment. Furthermore, the intervention will include a family intervention program followed up by support to one individual family caregiver. The primary outcomes are increased work or study rate at 6-month follow-up. Moreover, a budget impact analysis and possibly a cost utility analysis of the intervention will be performed The program is one of the first to include a comprehensive and target VR intervention including multiple parties such as the municipalities, a specialized rehabilitation team, and patients' own family caregivers. If this intervention is proven successful when compared to the conventional VR, it will provide evidence for a manual-based individualized holistic approach in returning to work after an ABI. The first hypothesis of the study is that more participants allocated to the VR intervention group will have a significant higher employment/study rate (measured in hours) at 6-month follow-up when compared to participants receiving the conventional VR program provided by the municipalities (control group). The second hypothesis is that health-related quality of life (HRQoL) and disability among the participants as well as the HRQoL and caregiver burden among the caregivers are significantly improved at the end of the VR intervention and at 6-month follow-up when compared to the conventional VR program. Finally, a budget impact and possibly a cost utility analysis will be performed.