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Contusions clinical trials

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NCT ID: NCT05771285 Completed - Pain Clinical Trials

Cold Application on the Subcutaneous Injection

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

The goal of this clinical trial is to compare the effect of cold application at different periods of time on the occurrence of bruising, haematoma and pain in the subcutaneous low molecular weight heparin (LMWH) injected patients.

NCT ID: NCT04908748 Completed - Clinical trials for Soft Tissue Injuries

Efficacy and Safety of Esflurbiprofen Hydrogel Patch in the Treatment of Local Acute Pain

Start date: May 20, 2021
Phase: Phase 2
Study type: Interventional

Objective of this study is: to determine efficacy and safety of a Esflurbiprofen Hydrogel Patch compared to placebo in patients with acute strains, sprains or bruises of the extremities following blunt trauma, e.g. sports injuries. to demonstrate that the Esflurbiprofen Hydrogel Patch is superior to placebo, and that the patch has acceptable local tolerability.

NCT ID: NCT04677712 Completed - Cellulite Clinical Trials

Effects of Mitigation Treatments on Bruising of CCH-aaes Treatment of Buttock Cellulite

MOBI
Start date: December 28, 2020
Phase: Phase 4
Study type: Interventional

This study will investigate treatments that may mitigate bruising after QWO™ (Collagenase clostridium histolyticum [CCH]-aaes) treatment of cellulite in the buttocks.

NCT ID: NCT04518904 Completed - Clinical trials for Pulmonary Contusion , Chest Trauma , Prediction Model

Establishment of a Prognosis Prediction Model and Scoring Criteria of Pulmonary Contusion Caused by Severe Thoracic Trauma

Start date: January 1, 2014
Phase:
Study type: Observational

Pulmonary contusion caused by severe thoracic trauma is a complex disease. Some patients may be secondary to severe complications such as pulmonary infection or even acute respiratory distress syndrome. At present, there have been no reports on related studies based on Chinese population. In this study, 800 patients with pulmonary contusion will be retrospectively investigated to determine the risk factors and independent risk factors of their poor prognosis, and to construct a prognosis prediction model and scoring criteria.

NCT ID: NCT04331405 Completed - Clinical trials for Spinal Cord Contusion

Allogeneic Cord Blood Cells for Adults With Severe Acute Contusion Spinal Cord Injury

Start date: March 18, 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Study evaluates the safety and primary efficiency of systemic (i.v.) allogeneic human umbilical cord blood mononuclear cell infusions in patients with severe acute contusion spinal cord injury (ASIA A/B). 20 patients were included. Half of patients received cell therapy in addition to standard therapy, while the other half received standard therapy only.

NCT ID: NCT03233321 Completed - Pain Clinical Trials

Effectiveness of Dry Cold Application on Pain and Bruise at the Subcutaneous Injection Site Among Patients Admitted in ICU

Start date: November 2015
Phase: N/A
Study type: Interventional

The study evaluate the effectiveness of dry cold application on pain intensity and bruise at the subcutaneous injection site among patients admitted in medical I.C.U. Purposive sampling technique was used to select 60 hospitalized patients (30 in experimental and 30 in comparison group). Dry cold was applied to the subcutaneous injection site using ice bag filled with crushed ice with half table spoon of salt for 20 minutes after the administration of injection and no intervention was given in comparison group.

NCT ID: NCT03090308 Completed - Pulmonary Contusion Clinical Trials

Pulmonary Contusion Flail Chest Complex

Start date: April 2013
Phase: N/A
Study type: Observational [Patient Registry]

The study included 20 adult patients presented by multiple fractured ribs (flail segment) with thoracic trauma severity score (TTSS) between 5 and 15. All patients received mid-thoracic epidural analgesia with 0.125% Bupivacaine and 1 μg/ml fentanyl. The patients were ventilated using non-invasive positive pressure ventilation (NIPPV). Follow up arterial blood gases, chest X-ray and CT scan were obtained. Parameters to be recorded: Patient's characteristics and clinical data including pulmonary contusion, number of fractured ribs, pleural involvement, PaO2/FiO2 ratio on admission, weaning outcome, duration of NIPPV, length of stay in ICU (LOS ICU), complications and mortality rate.

NCT ID: NCT02858544 Completed - Brain Injuries Clinical Trials

Concussion in Motor Vehicle Accidents: The Concussion Identification Index

CIDI
Start date: November 2013
Phase: N/A
Study type: Observational

The primary goal of this study is to provide clinicians with a brief, patient self-administer instrument yielding a single composite score that reliably correlates with objective findings on standardized neurocognitive assessment for concussion.

NCT ID: NCT02429141 Completed - Clinical trials for Crush Injury Wrist or Hand

Periarterial Injection Versus Multiple Periveural Injection

Start date: January 2015
Phase: N/A
Study type: Interventional

In the transarterial technique for axillary brachial plexus block, the axillary artery is intentionally punctured to indicate placement of the needle within the neurovascular sheath; local anesthetic is then injected deep and superficial to the axillary artery.

NCT ID: NCT02368366 Completed - Brain Injuries Clinical Trials

Comparative Effectiveness of Family Problem-Solving Therapy (F-PST) for Adolescent TBI

Start date: November 2014
Phase: N/A
Study type: Interventional

Traumatic brain injury (TBI) is the most common cause of acquired disability in youth and a source of significant morbidity and family burden. Novel behavior problems are among the most common and problematic consequences, yet many youth fail to receive needed psychological services due to lack of identification and access. Linking youth with TBI to effective treatments could improve functional outcomes, reduce family burden, and increase treatment satisfaction. The investigators overarching aim is to compare the effectiveness, feasibility, and acceptability of three formats of family problem solving therapy (F-PST) for improving functional outcomes of complicated mild to severe adolescent TBI: therapist-guided, face-to-face; therapist-guided online; and self-guided, online F-PST.