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Ultrasonography, Interventional clinical trials

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NCT ID: NCT05264935 Recruiting - Clinical trials for Rotator Cuff Tendinitis

Ultrasound-guided Lavage of Calcific Deposits of the Rotator Cuff

Kalklavage
Start date: May 1, 2022
Phase:
Study type: Observational

The primary goal of the study is to assess ultrasonographic Power Doppler signals after ultrasound-guided puncture and lavage of rotator cuff calcific tendinitis of the shoulder. Secondary outcomes are sonographic features like the course of residual calcific material and the course of tendon healing als well as the clinical symptoms of the patient.

NCT ID: NCT04317976 Completed - Clinical trials for Ultrasonography, Interventional

Ultrasound Guided Cricoid and Paralaryngeal Pressure

Start date: February 1, 2019
Phase: N/A
Study type: Interventional

The primary objective is to study impact of upper airway ultrasonography in guiding anaesthetic assistant into providing accurate cricoid pressure, or both cricoid and paralaryngeal pressure in those with oesophagus deviation, achieving sonographic proven oesophageal occlusion compared to those without ultrasound guidance.

NCT ID: NCT03996733 Completed - Education Clinical Trials

Using A Gelatin-Based Model In USG-Guided Jugular Venous Catheter Placement Training

Start date: July 1, 2019
Phase: N/A
Study type: Interventional

An education model with a homemade jugular venous catheterization model will be compared to the conventional training model for ultrasound-guided central jugular line catheterization. The study will include 60 residents to be divided into two groups with stratified random sampling. Training session for the control group (Group 2) will include a lecture about the subject, a demo video presentation, and practice of visualization of right jugular vein on a real human subject. Training session for the model group (Group 1) will include the same as GControl with the addition of the puncture practice on the homemade jugular venous catheterization model(HJVCM) with ultrasound guidance. Both groups will be tested with another HJVCM individually and the results of the success and fail parameters will be compared.

NCT ID: NCT03518450 Completed - Pain, Postoperative Clinical Trials

Femoral Triangle Block: Early Mobilization and Postoperative Analgesia After Total Knee Arthroplasty

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

The objective of this trial is to compare the efficacy of three different nerve blocks as an analgesic option after total knee arthroplasty (TKA), based on muscle strength, mobilization and pain. The Adductor Canal Block has been proposed as an equally effective technique to the Femoral Nerve Block in terms of pain control after a TKA, with the benefit of preserving muscle function. We hypothesize that a block performed at the apex of the femoral triangle would best balance analgesia with quadriceps function.

NCT ID: NCT02584530 Completed - Clinical trials for Peripheral Venous Catheterization

Comparing Ultrasound Guided PICC Line Insertion in Neonates With Standard Procedure

Start date: July 2016
Phase: N/A
Study type: Interventional

This is a randomized controlled study comparing US guided vs standard procedure for PICC line placement in newborns admitted to Children's Hospital of Eastern Ontario Neonatal Intensive Care Unit who require a PICC line. Patients will be randomized using REDCap randomization module (stratified by gestational age < 28 weeks and >= 28 weeks and blocked to ensure approximate balance with each stratum) into two arms. - Arm 1: PICC line insertion procedure using anatomical landmarks and tip placement will be confirmed by X-ray (current standard); Arm 2: US guided PICC line insertion procedure and tip placement confirmation by both US and X-ray. Sample size of 33 infants per group would achieve greater than 80% power to detect a difference between groups. Primary outcome: Time to complete the standard versus the US-guided procedure. Secondary outcomes (comparison between two arms): The number of total "venipuncture" attempts needed to place a PICC line Number of tip manipulations after complete insertion Proportion of successful tip placement

NCT ID: NCT01593280 Recruiting - Cesarean Section Clinical Trials

TAP Catheters Versus Intrathecal Morphine for Cesarean Section

Start date: May 2012
Phase: N/A
Study type: Interventional

Morphine, when given as part of spinal anesthesia, is associated high incidence of nausea and pruritus, which may affect quality of recovery. The investigators hypothesize that long-acting local anesthetic infusions via TAP catheter can provide better quality of recovery after cesarean section than spinal morphine.

NCT ID: NCT01589796 Recruiting - Adult Clinical Trials

Medial Versus Traditional Approach to US-guided TAP Blocks for Open Inguinal Hernia Repair

Start date: April 2012
Phase: N/A
Study type: Interventional

Pain relief after open inguinal hernia repair could be improved by administration of TAP block or ilioinguinal/iliohypogastric nerve block. It is unclear which one works better. The investigators hypothesize that doing TAP block closer to the middle of the abdomen would result in improved pain relief due to simultaneous block of ilioinguinal/iliohypogastric nerves.

NCT ID: NCT01200056 Completed - Coronary Disease Clinical Trials

Virtual Histology Findings and Effects of Varying Doses of Atorvastatin Treatment

VENUS
Start date: August 2007
Phase: Phase 4
Study type: Interventional

While statin treatment may induce plaque regression, the effect of statin on plaque composition with varying doses is unknown. This study assessed such effects by volumetric virtual histology intravascular ultrasound (VH-IVUS). In this prospective, randomized, double-blinded pilot study, statin-naïve patients with stable angina requiring percutaneous coronary intervention (PCI) were randomized to receive 6 months of either atorvastatin 10mg or 40 mg daily. VH-IVUS was performed in all non-PCI lesions at baseline and 6 months; all analyses were performed by core laboratory.

NCT ID: NCT01057355 Withdrawn - Clinical trials for Pancreatic Neoplasms

Endoscopic Ethanol Ablation of Communicating Pancreatic Cystic Neoplasms

Start date: January 2010
Phase: Phase 1
Study type: Interventional

Pancreatic cysts are common, and some pancreas cysts have malignant potential. Usual treatment of these cysts is either observation or surgical removal of part or all of the pancreas. Minimally invasive treatment via endoscopy has been described, using endoscopic ultrasound (EUS) guided ethanol injections. Such studies exclude cysts that communicate with the main pancreatic duct, to avoid burning the main pancreatic duct with ethanol. In this study, pancreas cysts communicating with the main pancreas duct are treated with ethanol via endoscopic retrograde cholangiopancreatography (ERCP) and/or EUS.