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Active clinical trials for "Hematoma"

Results 121-130 of 236

Laparoscopic Versus Transvaginal Cuff Closure

Vaginal Cuff DehiscenceVaginal Hematoma1 more

It is still debatable whether that the transvaginal approach to vault closure or laparoscopic suturing are associated with lower risks of vaginal cuff complications . This study aims to compare the two approaches of closure of the vaginal cuff at the end of total laparoscopic hysterectomy as regards the vaginal cuff complications .

Completed9 enrollment criteria

Vacuum Assisted Closure as a Treatment for Draining Hematomas

Draining Hematoma

This project is designed as a prospective, randomized, comparative study evaluating the use of a negative pressure vacuum device in treating draining hematomas following traumatic injury.

Completed11 enrollment criteria

The Swedish Study of Irrigation Fluid Temperature in the Evacuation of Chronic Subdural Hematoma...

Chronic Subdural Hematoma

The study will be a multicenter randomised controlled trial of the use of irrigation fluid of body temperature versus irrigation fluid of room temperature during burr hole evacuation of chronic subdural hematoma.

Completed6 enrollment criteria

Comparing TR Band to Statseal in Conjunction With TR Band II

Arterial OcclusionCardiovascular Diseases4 more

The purpose of this clinical study is to compare how well two different devices for achieving hemostasis perform in patients undergoing transradial procedures. Both devices are approved by the FDA for this use, and have already been used by clinicians on patients undergoing transradial procedures. It is believed that the use of both devices in combination compared to the hemostasis band (TR band) alone will shorten the time that it takes to 'seal' the artery, resulting in a shorter period of time that you would need to wear the hemostasis band.

Completed17 enrollment criteria

Comparing Perclose to Statseal With Perclose in Transcatheter Aortic Valve Replacement Arteriotomy...

Arterial OcclusionCardiovascular Diseases1 more

The purpose of this clinical study is to compare how well two different devices achieve hemostasis in patients undergoing a transfemoral transcatheter aortic valve replacement. Both devices are approved by the FDA for this use, and have already been used by clinicians on patients undergoing transfemoral procedures. It is believed that the use of both devices in combination compared to the Perclose alone will shorten the time that it takes to 'seal' the artery, resulting in a shorter period of time that manual pressure will be held, shorter procedure time and less complications after the procedure.

Completed11 enrollment criteria

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

Hemodialysis ComplicationDialysis; Complications5 more

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.

Completed2 enrollment criteria

A Prospective Randomized Study Evaluating the Recurrence Rate of Chronic Subdural Hematoma After...

Chronic Subdural Hematoma

The aim of our study is to investigate in randomized controlled fashion whether the recurrence and complication rate, after insertion of subperiosteal drainage in the treatment of chronic subdural haematoma, is higher compared to insertion of subdural drainage. We hypothesize that patients treated with a subperiosteal drainage do not show higher recurrence rates than those treated with a subdural drainage, and suffer less complications.

Completed5 enrollment criteria

Investigation of Clot in Ischemic Stroke and Hematoma Evacuation

Ischemic StrokeIntracranial Hematoma

The aim of the study is to collect and analyze specimen from ischemic stroke patients undergoing thrombectomy procedures and from patients undergoing minimally invasive surgery for intracranial hematoma evacuation.

Active6 enrollment criteria

Antibiotic Prophylaxis for TEVAR

Aortic DissectionAortic Diseases4 more

The infection rate of thoracic endovascular aortic repair (TEVAR) is unknown due to a lack of epidemiological data. The rate currently available comes from researches conducted decades ago, when open surgery was the standard of care. Because of the potentially fatal consequences of a stent graft infection in the thoracic aorta, the investigators tend to prescribe antibiotic prophylaxis for at least three days. In this study, the investigators are going to collect data on patients receiving TEVAR in the past five years and provide the following information: a. the infection rate (MAGIC classification), b. the rate of fever, c. the results of the lab tests, such as the WBC count and C-reaction protein. d. risk factors associated with infection and fever.

Active10 enrollment criteria

Strategy of Continued Versus Interrupted Novel Oral Anti-coagulant at Time of Device Surgery in...

Hematoma

The purpose of this study is to determine the best strategy to manage novel oral anti-coagulants (NOACs) at the time of pacemaker or defibrillator surgery. The Investigators hypothesize that performing device surgery without interruption of the novel oral anti-coagulant will result in a reduced rate of clinically significant hematoma.

Completed10 enrollment criteria
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