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Catheter Related Complication clinical trials

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NCT ID: NCT05966909 Completed - Clinical trials for Catheter Related Complication

Incidence and Clinical Progression of Asymptomatic PICC-Related Thrombosis in Solid Cancer Patients

Start date: January 1, 2020
Phase:
Study type: Observational

In this prospective cohort study, the investigators evaluated the incidence of superficial vein thrombosis, deep vein thrombosis, and fibroblastic sleeve formation in solid cancer patients undergoing chemotherapy. The study aimed to shed light on the clinical progression of venous thrombosis in cancer patients with central venous catheters, with a particular focus on certain cancer types associated with a higher risk of venous thromboembolism (VTE). The investigators believe that such findings hold significant clinical relevance as a substantial portion of the study population was affected by pancreatic cancer, a cancer type known to carry a high risk of thrombotic events. This research adds valuable insights into understanding asymptomatic PICC-related thrombosis in this specific subgroup of cancer patients, which can aid in developing effective management strategies for venous access in this challenging population. The study employed an ultrasound-guided approach for follow-up at 30 and 90 days after catheter insertion, enabling us to detect and treat asymptomatic PICC-VTE in a timely manner. Identifying independent risk factors for catheter-related thrombosis, including age and cancer type, has further enhanced the clinical applicability of our findings.

NCT ID: NCT05948878 Completed - Clinical trials for Catheter Related Complication

An Innovative Taping Technique for Improved Intravenous (IV) Catheter Securement

Start date: July 28, 2023
Phase: N/A
Study type: Interventional

This is a prospective, single-blinded, randomized study to assess the ability of taping methods used to secure intravenous (IV) catheters to resist the IV from being pulled away from the skin. Participants will have IV catheters taped on top of the skin (without insertion into the skin) using three taping methods, BCH Emergency Department (BCH ED), Chevron, and our novel method. Six measurements will be obtained per subject (3 random taping methods measuring their resistance to force in two directions, retrograde direction or towards the wrist and 90-degree angle to the arm).

NCT ID: NCT05130762 Completed - Clinical trials for Catheter Related Complication

An Observational Study to Evaluate BD PureHubâ„¢ Disinfecting Cap Use on Needle-Free Connectors

Start date: January 31, 2022
Phase:
Study type: Observational

The study will collect use data of the Becton Dickinson (BD) PureHubâ„¢ Disinfecting Cap in combination with needle-free connectors, which are attached to vascular access devices (VAD).

NCT ID: NCT04814745 Completed - Clinical trials for Catheter Related Complication

Intrathecal Morphine for Radical Robot Assisted Prostatectomy (TORNADO)

TORNADO
Start date: July 7, 2020
Phase: N/A
Study type: Interventional

investigators aim to compare the efficacy of intrathecal morphine, intravenous tramadol and transversus abdominis plane block in the treatment of catheter related bladder discomfort syndrome in patients scheduled for robotic assisted laparoscopic prostatectomy

NCT ID: NCT04811430 Completed - Clinical trials for Catheter Related Complication

Efficiency, and Emergency Department Nurse Preference Between 2 Methods of Visualization: A Pilot Study

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

The purpose of this study was to assess the impact of a continuous needle tracking system on the accuracy, speed, and quality of ultrasound-guided peripheral venous catheter insertion.

NCT ID: NCT04772209 Completed - Clinical trials for Catheter-Related Infections

Comparison of Effectiveness and Complications of Catheter Lock Solutions in Non-tunneled Hemodialysis Catheters

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

In our study, investigators will investigate the effectiveness and complications of two catheter lock solutions one of which is the standard heparin routinely used in comparison to Sodium bicarbonate. Both solutions were used but not compared head to head. Investigators aim to compare both solutions in terms of catheter lumen patency and their effect on catheter-related infections.

NCT ID: NCT04683302 Completed - Clinical trials for Catheter Related Complication

3D Guided Internal Jugular Vein Catheterization

3D Givenchy
Start date: March 15, 2021
Phase: N/A
Study type: Interventional

Central venous catheterization through the jugular vein is a standard procedure for cardiothoracic surgical patients. Ultrasound (US) guidance is preferred and compared to traditional landmark approach decreases complications and increases success rate. Both long and short axis views are used for obtaining access, both with their own advantages and shortcomings. Complications have also not completely diminished with the use of US. The investigators propose a new technique using 3D biplanar imaging, combining advantages from both long and short axis views in one image, enabling more successful procedures and a lower complication rate

NCT ID: NCT04454970 Completed - Transgenderism Clinical Trials

Safe Access for Bladder Entry in Transgender Men Following Penile Reconstruction

SAFE
Start date: September 16, 2022
Phase: N/A
Study type: Interventional

Inserting a urinary catheter in transgender men following penile reconstruction is difficult and usually requires specialist input. Specialist input may not always be readily available and clinicians may resort to suprapubic catheterisation with the associated risk of injury to the bowel or blood vessels. There is a need for an evidence-based protocol to guide clinicians faced with having to catheterise one of these patients. The investigators will evaluate how successful a specialised catheter (Urethrotech UCD®) is compared with a standard Foley catheter for catheterisation of these patients. The Urethrotech UCD® is already used for difficult catheterisation in cisgender men. Transgender men undergoing insertion of an inflatable penile prosthesis under general anaesthesia will be recruited and randomly assigned to have either the Urethrotech UCD® or Foley catheter for the first attempt at urethral catheterisation (required for standard care). If unsuccessful, flexible cystoscopy will be performed and a Foley catheter will be inserted over a guidewire. The catheter is generally removed the next day prior to discharge from hospital. Patients will be followed-up in 30 days by phone.

NCT ID: NCT04314050 Completed - Clinical trials for Catheter Related Complication

Comparison of Tramadol and Dexmedetomidine in the Prevention of Urinary Catheter Discomfort in Urinary Surgery

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

The investigators aimed to compare the effects of tramadol and dexmedetomidine, which are commonly used in anesthesia, on preventing catheter-related bladder discomfort.

NCT ID: NCT03955653 Completed - Clinical trials for Catheter Related Complication

Fluoroscopic-Guided Micropuncture Technique for Common Femoral Artery Access

ACCESS
Start date: April 30, 2019
Phase: N/A
Study type: Interventional

The main objective of this proposed study is to examine if oblique projection (20- degrees right anterior oblique (RAO) for right femoral artery access or 20-degree left anterior oblique (LAO) for left femoral artery access) is superior to anterior projection (AP) for femoral artery access in zone 2-4 and thereby resulting in lower risk of access related complications.