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Trauma clinical trials

View clinical trials related to Trauma.

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NCT ID: NCT03681041 Recruiting - Trauma Clinical Trials

Pancreatic Injury and Corresponding Management Outcome (PICO)

Start date: January 1, 2000
Phase:
Study type: Observational

Pancreatic injury is a relatively rare and result in significant morbidity and mortality. Estimates for the incidence of pancreatic injury range from 0.2-12% of abdominal traumas. Many factors, such as patient stability, the acuity of concomitant life-threatening injuries, and the need for damage control procedures must therefore be balanced when considering the proper approach to pancreatic injury management. However, few prospective studies have investigated the perioperative management of patients with pancreatic trauma.

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: NCT03658603 Not yet recruiting - Trauma Clinical Trials

Thoracodorsal Artery Perforator Flap Versus Conventional Free Flaps

Start date: October 3, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the efficacy of the thoracodorsal artery perforator flap versus other conventional free flaps for reconstruction of soft tissue defects.

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: NCT03643718 Recruiting - Trauma Clinical Trials

Web-based International Register of Emergency Surgery and Trauma

WIRES-T
Start date: July 2020
Phase:
Study type: Observational [Patient Registry]

The WIRES-T project (Web-based International Registry of Emergency General Surgery and Trauma) has been set up to allow to all the EGS (Emergency General Surgery) and Trauma surgeons to register their activity and to obtain a worldwide register of traumatic and non traumatic surgical emergencies. This will give the opportunity to evaluate results on a macro-data basis and to give index allowing stratifying, evaluating and improving the outcomes.

NCT ID: NCT03622632 Active, not recruiting - Inflammation Clinical Trials

Pilot Study to Measure Uric Acid in Traumatized Patients: Determinants and Prognostic Association

Start date: September 30, 2018
Phase:
Study type: Observational

The goal of this project, is to better understand the fluctuation of the level of uric acid in traumatized patients by making serial measurements during their hospitalization in the intensive care unit. In addition, the determinants (e.g. type of trauma, diseases, interventions) of the blood level of uric acid and its association with the development of organ failure will be sought.

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: NCT03574376 Recruiting - Trauma Clinical Trials

Liposomal Bupivacaine Intercostal Nerve Block vs Thoracic Epidural for Regional Analgesia in Multiple Rib Fractures

Start date: August 29, 2018
Phase: Phase 4
Study type: Interventional

Management of traumatic rib fractures continues to be a challenge for trauma surgeons. Currently, many analgesic options are available to patients suffering from rib fractures. Formulations currently used for conventional intercostal nerve blocks (CINB) are relatively safe, do not require additional equipment or specialized anesthesia personnel, do not require catheter repositioning, and provide improved analgesia immediately over the aforementioned systemic therapies. A goal of these authors to introduce an additional safe option for extended local analgesia in the setting of multiple rib fractures given the inconclusive evidence supporting or refuting the current standard of care

NCT ID: NCT03572309 Recruiting - Trauma Clinical Trials

Incidence of Trauma Induced Coagulopathy in Patients With Prehospital Administration of Fibrinogen

TICAF
Start date: July 23, 2018
Phase:
Study type: Observational

The purpose of the study is to find out the incidence of trauma induced coagulopathy in patients with severe trauma who received fibrinogen prior admission to emergency department during prehospital care.

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.