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Wounds and Injuries clinical trials

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NCT ID: NCT05175872 Completed - Trauma Injury Clinical Trials

Factors Affecting Mortality and Morbidity in Trauma Patients Followed in Intensive Care Unit

trauma
Start date: October 14, 2019
Phase:
Study type: Observational

In this study, the demographic and clinical characteristics of trauma patients followed up in the Intensive Care Unit of the Anesthesiology and Reanimation Clinic of the Health Sciences University Okmeydanı Training and Research Hospital for a 2-year period were evaluated prospectively to determine the morbidity and mortality rates and to determine the factors affecting these rates. data.

NCT ID: NCT05175781 Completed - Chest Trauma Clinical Trials

Sedation for Non-invasive Ventilation in Blunt Chest Trauma

Start date: January 18, 2022
Phase: N/A
Study type: Interventional

Effectiveness of sedation using dexmedetomidine and ketamine to facilitate non-invasive ventilation sessions which improve overall outcome after blunt chest trauma

NCT ID: NCT05175183 Completed - Sports Injury Clinical Trials

Epidemiology of Speed Skating-related Injuries

Start date: December 1, 2021
Phase:
Study type: Observational

Speed skating is a sport in which there´s a lack of epidemiological studies. In line with the well-established model of sports injury prevention research proffered by van Mechelen, the first stage in this process is establishing the extent of the problem i.e. injury incidence, severity and burden. Through an online survey filled by semiprofessional athletes, it is posible to obtain all this important information. This way, it will be possible to fulfill a gap in the literature and take action in the near future in order to reduce the prevalence of injuries in this sport.

NCT ID: NCT05172882 Completed - Analgesia Clinical Trials

Efficacy of Transversalis Fascia Plane Block Versus Wound Infiltration in Varicoselectomy Surgery

Start date: November 15, 2021
Phase: N/A
Study type: Interventional

Before surgery, patients will be divided into 2 groups as transversalis fascia plane block will be applied and skin infiltration will be applied. Post-operative analgesic procedures will be applied to patients receiving general anesthesia. Postoperative analgesic consumption and pain scores of the patients will be evaluated.

NCT ID: NCT05171868 Recruiting - Stress Clinical Trials

Eye Movement Desensitization and Reprocessing (EMDR) for Police Personnel

Start date: May 20, 2022
Phase: N/A
Study type: Interventional

Objectives: 1. To examine the feasibility of Eye Movement Desensitization and Reprocessing (EMDR) as an intervention to reduce psychological trauma and stress amongst police officers in Pakistan. 2. To test whether reducing stress and psychological trauma reduces suicidal ideation in police officers. 3. To explore participants' experiences with EMDR Intervention. Study design and setting: The study will be a mixed-method feasibility randomized controlled trial of EMDR as an intervention in treating symptoms such as stress, trauma and suicidal ideation in police officers. The study will be conducted in five major cities in Pakistan: Rawalpindi, Karachi, Peshawar, Quetta, and Lahore. Sample size: A total of N=80 eligible police officers will be recruited and randomized in the study.

NCT ID: NCT05171699 Recruiting - Sepsis Clinical Trials

Effect of Electroacupuncture in Patients With Sepsis Associated Brain Injury

Start date: April 25, 2022
Phase: N/A
Study type: Interventional

To investigate the effect of electroacupuncture on patients with sepsis-associated brain injury.

NCT ID: NCT05171673 Recruiting - Clinical trials for Soft Tissue Injuries

Study of PK and Safety of the LicartTM Topical System in Pediatric and Adult Participants With Minor Soft Tissue Injury

Start date: October 31, 2021
Phase: Phase 3
Study type: Interventional

A multi-center, prospective, open-label, controlled study of the pharmacokinetics and safety of the LicartTM topical system in pediatric and adult participants with minor soft tissue injuries. 150 male and female participants aged 6-16 and 18-45 with soft tissue injuries meeting the following criteria will be enrolled to evaluate the pharmacokinetics and safety of the Licart topical system in pediatric and adult participants with minor soft tissue injuries over a 14-day treatment course. The analgesic effects will also be evaluated of the topical system in pediatric and adult participants with minor soft tissue injuries over a 14-day treatment course. To collect principal investigator-reported global response to therapy.

NCT ID: NCT05171400 Recruiting - Wound Healing Clinical Trials

A New Drug Delivery System - Silk Fibroin Film Loaded or Not With Insulin on Palatal Mucosa Wound Healing

Start date: July 2, 2021
Phase: N/A
Study type: Interventional

The aim of the present study is to evaluate using clinical, patient-centered, immunological, microbiological, and histological parameters, the effect of silk fibroin films loaded or not with insulin in the repair of palatal mucosa open wounds.

NCT ID: NCT05171010 Completed - Clinical trials for Traumatic Brain Injury

Geri-TBI: A Prospective Multi-center Evaluation of Geriatric Patients With Traumatic Brain Injury

Start date: November 29, 2017
Phase:
Study type: Observational

This multicenter prospective observational study is designed to prospectively record data on patients who are managed per institutional standard of care. The objectives of this study are to establish an aggregate database of information on baseline clinical and demographic characteristics, medication use, markers of frailty, injury characteristics, management strategies, and outcomes following TBI in geriatric patients, determine best practices for management of geriatric patients with TBI, and establish how markers of frailty correlate with outcome in geriatric patients with TBI.

NCT ID: NCT05169814 Recruiting - Wound Heal Clinical Trials

Micro/Nanobubbles (MNBs) for Treatment of Acute and Chronic Wounds

MNB
Start date: October 9, 2021
Phase: Early Phase 1
Study type: Interventional

The purpose of this study is to assess the safety and efficacy of Micro/nanobubbles (MNB's) for the healing of acute and chronic wounds.