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Hematoma clinical trials

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NCT ID: NCT05553821 Completed - Clinical trials for Clinical Nursing Research

Effect of Cold Pressure in the Prevention of Hematoma and Ecchymosis

Start date: November 3, 2021
Phase: N/A
Study type: Interventional

Coronary Artery Disease (CAD) is the most common cardiovascular system disease. According to the World Health Organization data, CAD ranks first among the top 10 causes of death. According to the 2014 data of the Turkish Statistical Institute (TUIK), deaths due to circulatory system diseases are in the first place with 40.4%, and 39.6% of this is ischemic heart diseases. The prevalence of CAD in Turkey is 12% in women and 14% in men. The diagnosis of CAD is largely made on non-invasive tests. Coronary angiography (CAG) is recommended for definitive diagnosis and detection of coronary stenosis. CAG is defined as the manual delivery of contrast material through a catheter sent to the coronary arteries under fluoroscopy and recording the resulting image on a CD. With special catheters advanced through a plastic sheath called a sheath placed in the access tract, contrast agents are administered separately to the left main coronary (LDA) and right main coronary arteries (RCA), and images of the coronary arteries are taken in multiple positions. Complications related to diagnostic and therapeutic CAG are rare, but vary according to the patient's condition, operator's experience, and the type of procedure. The most common vascular complications are bleeding, hematoma, ecchymosis, pseudoaneurysm, retroperitoneal hemorrhage, arteriovenous fistula. Preventing complications before they develop is actually shown as the most successful treatment. For this reason, it is recommended to use a small-diameter catheter during CAG, to enter the main femoral artery carefully, to interrupt anticoagulant treatment before the procedure, to apply manual compression to the area for at least 20 minutes after the procedure, and to use percutaneous closure devices, which is another method. After the procedure, pressure is applied with a sandbag, manual compression, and a pneumatic compression device. In the sandbag method, a 3-4.5 kg sandbag is placed after the bleeding is controlled by manual pressure on the femoral region where the intervention is made. During this period, the patient's movements are restricted and he is asked to lie flat on his back. In the use of the pneumatic compression device, a pneumatic compression device (closepad) with a transparent window and balloon incision is placed to maintain the compression on the femoral artery after a short period of manual compression. However, it is not preferred because of the risk of embolism and high cost. In addition to pressure applications, local cold application is effective in preventing perivascular complications. Cold application controls bleeding by reducing capillary blood flow and capillary permeability by vasoconstriction of arterioles. In addition, it reduces the flow rate of the blood and increases its viscosity, thereby making it coagulate. It controls bleeding by blood coagulation, reduced capillary permeability and metabolic requirements. This situation reduces the development of ecchymosis and hematoma. Considering this information, cold application can be preferred for the prevention of hematoma and ecchymosis, which are the most common complications after CAG, because it is practical, inexpensive and comfort-enhancing. The number of studies in the literature in which cold application and pressure application are used together is limited. Based on this information, the current study was planned to evaluate the effectiveness of cold pressure application for the prevention of hematoma and ecchymosis in the CAG intervention area. The hypotheses of the research; H0: Cold pressure application has no effect on the prevention of hematoma and ecchymosis in the CAG intervention area. H1: Cold pressure application has an effect on the prevention of hematoma and ecchymosis in the CAG intervention area.

NCT ID: NCT05500768 Completed - Pocket Hematoma Clinical Trials

Efficacy of the hYpothermic Compression Bandage in the Surgical Wound of Cardiac Devices

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

The aim of this study is to evaluate the efficacy of hypothermic compression bandaging versus conventional compression bandaging, for the prevention of surgical wound hematoma of cardiac implementable electronic devices in patients undergoing chronic oral anticoagulant therapy and/or oral antiplatelet therapy.

NCT ID: NCT05446987 Completed - Back Pain Clinical Trials

Position Change and Back Massage Versus Early Ambulation on Post Transfemoral Coronary Angiography Complications

Start date: March 1, 2017
Phase: N/A
Study type: Interventional

The study aimed to assess the effect of position change and back massage versus early ambulation on post transfemoral coronary angiography complications.

NCT ID: NCT05439694 Completed - Cesarean Section Clinical Trials

TXA Soaked Gelatin Sponge to Reduce Rectus Sheath Hematoma After C.S. in Patients Using Warfarin

Start date: July 3, 2022
Phase: Phase 4
Study type: Interventional

The aim of this randomized controlled study is to demonstrate the effect of Local application of TXA impregnated in a gelatin sponge in reducing Rectus sheath hematoma formation in patients treated with warfarin following cesarean section.

NCT ID: NCT05410691 Completed - Clinical trials for Hemodialysis Complication

Handheld Ultrasound-guided Cannulation of Difficult Haemodialysis Arteriovenous Access by Renal Nurses

Start date: January 1, 2021
Phase: N/A
Study type: Interventional

Cannulation of complex arteriovenous fistula (AVF) or graft (AVG) is a challenge to renal nurses. Ultrasound (US) guidance on central and peripheral venous access visualisation has been widely adopted in nephrology and shown to reduce complications of vascular interventions. With broader adoption of handheld US devices in clinical services, renal nurses could acquire this point-of-care technique to increase the successful cannulation rate while facilitating confidence build-up during training and practice. We aim to evaluate the use of handheld US on difficult AVF/AVG cannulation in a hospital-based dialysis unit.

NCT ID: NCT05204420 Completed - Gastric Hemorrhage Clinical Trials

Spontaneous Gastric Intramural Hematoma: Case Report and Literature Review

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

Patient previously healthy found to have spontaneous gastric intramural hematoma

NCT ID: NCT05190276 Completed - Clinical trials for Symptomatic Epidural Hematoma After Cervical Spine Surgery

Incidence and Risk Factors of Symptomatic Epidural Hematoma After Cervical Spine Surgery

Start date: January 1, 2009
Phase:
Study type: Observational

The incidence and correlation of symptomatic epidural hematomas after cervical spine surgery was reviewed and analyzed, then it will provide reference to avoid the occurrence of this complication for the future clinical work.

NCT ID: NCT05189561 Completed - Clinical trials for Traumatic Brain Injury

Near-infrared Spectroscopy (NIRS) for Intracranial Hematoma Detection

Start date: August 24, 2021
Phase: N/A
Study type: Interventional

Traumatic brain injury is a common neurosurgical emergency managed in all tertiary and secondary hospitals. Detecting the underlying pathology is a major challenge especially for surgical cases. The outcome differs if the early intervention is performed. Near-infrared spectroscopy (NIRS) based device will detect the hematoma at the bedside. It is not the replacement of a CT scan but can help in triage. This is a large-scale prospective study to establish the role of NIRS device in detecting intracerebral hematoma and correlate the finding with CT scan finding.

NCT ID: NCT05126394 Completed - Clinical trials for Local Anesthetic Toxicity

U/S Guided SAPB Versus Conventional IV Analgesics in Postoperative Pain Management in MRM

SAPB
Start date: March 10, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to compare the effect of ultra-sound guided serratus anterior plane block versus conventional IV analgesics in postoperative pain management in modified radical mastectomy (MRM)

NCT ID: NCT04961424 Completed - Thoracic Surgery Clinical Trials

Risk Factors for Postoperative Spinal Epidural Hematoma Following Posterior Thoracic Spinal Surgery in a Single Institute

Start date: February 19, 2020
Phase:
Study type: Observational

This is a retrospective, observational single-center study. The studies is to investigate the incidence of posterior epidural spinal hematoma(PSEH) and recognize the risk factors for it in a cohort of patients undergoing posterior thoracic surgery in isolation.