Surgery Clinical Trials
45 studies are recruiting for surgery in the United States right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
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Studies, page 2
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Implementation Pilot of Preoperative CGA Before Major Surgery
The goal of this clinical trial is to test whether a new implementation package can help older adults prepare for major surgery. The main question it aims to answer is: Can the implementation package help give more people access to this resource? Participants will be in two groups: older adults who…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Wisconsin, Madison, Wisconsin
- Run by
- University of Wisconsin, Madison
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Terumo Aortic Global Endovascular Registry
Multi-arm, multi-center, open label, prospective observational registry designed to obtain safety and performance data on the use of CE marked and custom Terumo Aortic endovascular grafts.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Long Beach Memorial Medical Center, Long Beach, California
- Locations
- 58 in total
- Run by
- Vascutek Ltd.
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Effect of Fasting on Patient Outcomes After Wide-Awake, Local Anesthesia-only, No Tourniquet (WALANT) Procedures
The purpose of this study is to determine whether eating solid food prior to undergoing a wide awake local-only no tourniquet (WALANT) procedure reduces anxiety in patients or has any effect on outcomes. Patients will be split randomly into two groups and told whether to eat or fast before their pr…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- UCI Health Manchester Pavilion, Orange, California
- Run by
- University of California, Irvine
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Factor VIII Inhibitor Bypass Activity (FEIBA) Versus Fresh Frozen Plasma As First Line Therapy For Bleeding After Cardiac Surgery
Coagulopathic-induced bleeding after cardiopulmonary bypass in cardiac surgery patients is common and is associated with adverse outcomes in cardiac surgery. The hypothesis of the study is that FEIBA will be a more effective treatment than standard of care (FFP) in cardiac surgery patients who have…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- North Shore University Hospital, Manhasset, New York
- Run by
- Northwell Health
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Comparing Analgesic Regimen Effectiveness and Safety for Surgery for Kids Trial
This trial is being completed to compare two commonly used options to treat pain after discharge from surgery. Participants that undergo tonsil removal, gallbladder removal, and knee scope will be eligible to enroll. Eligible participants will be randomized to prescription of 1 of 2 groups of medic…
- Stage
- Phase 4
- Ages
- 12 to 20
- Site
- Children's Hospital Los Angeles (CHLA), Los Angeles, California
- Locations
- 4 in total
- Run by
- University of Michigan
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Green Light for Post-Operative Wellness
This is an unblinded, parallel group randomized controlled trial to evaluate bright green light as an adjunct therapy after surgery at UPMC Shadyside. The primary outcome measure will be pain intensity with secondary outcome measures including opioid requirements, sleep quality, mood, and overall p…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- UPMC Shadyside Hospital, Pittsburgh, Pennsylvania
- Run by
- Rebecca E Kotcher, MD
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The Neuralert Stroke Monitor Pilot Trial
This trial aims to demonstrate that the Neuralert Monitoring System will detect strokes before they would be identified by current standard of care. Each patient will be monitored for up to five days, depending on device connectivity or battery duration. Each monitoring session will consist of wear…
- Stage
- Not phased
- Ages
- 22 and older
- Site
- Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania
- Run by
- Neuralert Technologies LLC
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Prevent Cardiac Surgery Associated AKI Trial
Prevent CSA-AKI (Cardiac Surgery Associated Acute Kidney Injury) trial is a double blinded randomized controlled trial, 242 patients undergoing elective cardiopulmonary bypass surgery (CPB)will either receive a placebo or daily 1200 mg of Co enzyme Q10 (CoQ10) and 1000 mg of Glutathione (GSH), the …
- Stage
- Phase 2
- Ages
- 18 to 70
- Site
- George Washington University Hospital, Washington D.C., District of Columbia
- Run by
- George Washington University
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Physical Therapy After Endometriosis Excision
This is a randomized controlled pilot study comparing a home pelvic floor physical therapy program to routine post-operative care for patients undergoing endometriosis excisional surgery without hysterectomy. Quality of life and endometriosis symptoms will be compared following the recovery period.
- Stage
- Not phased
- Ages
- 18 to 50
- Site
- Oregon Health & Science University, Portland, Oregon
- Run by
- Oregon Health and Science University
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Evaluating a Dropless Postoperative Regimen After Cataract Surgery in a Vulnerable, County-hospital Population
The current postoperative cataract surgery eye drop regimen used at Zuckerberg San Francisco General Hospital (ZSFG) is a significant burden for its patient population, contributing to high rates of non-adherence and the development of postoperative complications. The investigators propose to repla…
- Stage
- Phase 4
- Ages
- 18 and older
- Site
- Zuckerberg San Francisco General Hospital and Trauma Center (ZSFG), San Francisco, California
- Run by
- University of California, San Francisco
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Post-Discharge Risk-Based Management in Patients Undergoing High-Risk Elective Major Cancer Operations (PRS II)
This is a randomized trial of intensified post-discharge surveillance (Intervention Arm) versus standard post-discharge surveillance (Control Arm).
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Fox Chase Cancer Center - Philadelphia, Philadelphia, Pennsylvania
- Run by
- Fox Chase Cancer Center
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Continuous Versus Single Injection Adductor Canal Blocks for Outpatient Total Knee Arthroplasty
This is a single-center pilot study to determine if an adductor canal continuous nerve block is superior to single injection nerve block following total knee arthroplasty. Investigators will randomize participants to either continuous nerve block or single injection nerve block for the adductor can…
- Stage
- Phase 4
- Ages
- 18 and older
- Site
- University of California, San Diego, La Jolla, California
- Run by
- University of California, San Diego
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The Pediatric Anesthesia Quality Improvement Project
The Study is designed to collect information about adverse events that occur in children undergoing anesthesia in participating hospitals. Demographic information will be collected on all anesthetics. An analysis of each adverse event will be performed and entered into the database. From this infor…
- Stage
- Not phased
- Ages
- Up to 21
- Site
- Phoenix Children's Hospital, Phoenix, Arizona
- Locations
- 37 in total
- Run by
- The Society for Pediatric Anesthesia
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Optimizing Pulsatility During Cardiopulmonary Bypass to Reduce Acute Kidney Injury
The objective is to determine the effectiveness of pulsatile flow during cardiopulmonary bypass to reduce the incidence of acute kidney injury after cardiac surgery. Investigators will also evaluate the safety and impact of pulsatile flow on clinical outcomes compared to non-pulsatile flow during c…
- Stage
- Not phased
- Ages
- 18 to 85
- Site
- University of Colorado Hospital, Aurora, Colorado
- Run by
- University of Colorado, Denver
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Geriatric Thoracic Surgery Ambulation Challenge
This study is examining collecting data on steps walked (ambulation) per day by thoracic surgery patients over the age of 65 years-old before surgery. The name(s) of the study device involved in this study is: * Fitbit inspire
- Stage
- Not phased
- Ages
- 65 and older
- Site
- Brigham and Women's Hospital, Boston, Massachusetts
- Locations
- 2 in total
- Run by
- Dana-Farber Cancer Institute
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Maestro 1.1 Post-Market Registry
The objective of the study is to observe the real-life usage of the Maestro Platform for surgical assistance in laparoscopic surgery.
- Stage
- Not phased
- Ages
- 18 to 100
- Site
- Rose Medical Center, Denver, Colorado
- Locations
- 12 in total
- Run by
- Moon Surgical
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Ultrasound Evaluation for Improving Patient Selection in vNOTES
Vaginal Natural Orifice Transluminal Endoscopic Surgery (vNOTES) is an emerging field in minimally invasive surgery. International consensus-based statement was recently published to help guide the basis for adopting vNOTES into clinical practice, including regarding patient selection. It was agree…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Texas, Houston, Texas
- Run by
- The University of Texas Health Science Center, Houston
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A Study of Bevonescein in Patients Undergoing Abdominopelvic Surgery
Feasibility study of Bevonescein to highlight Nerves and Ureter in patients undergoing Minimally Invasive Surgery
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- University of California San Diego, San Diego, California
- Run by
- Alume Biosciences, Inc.
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LaserEn: SOLTIVE™ Thulium Laser Fiber En Bloc Resection of Bladder Tumors
Conventional monopolar or bipolar transurethral resection of bladder tumors is the most common method for resection of a bladder mass. En bloc resection has demonstrated success in the literature utilizing different techniques and lasers, including utilizing the Ho:YAG and Tm:YAG lasers. A recent m…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Kansas Medical Center, Kansas City, Kansas
- Run by
- University of Kansas Medical Center
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RCT: Early Feeding After PEG Placement
Randomized controlled trial to establish evidence on which to base timing of enteral feeding after bedside PEG placement in ventilated Trauma and Surgical ICU patients.
- Stage
- Not phased
- Ages
- 18 to 100
- Site
- Carilion Roanoke Memorial Hospital, Roanoke, Virginia
- Run by
- Carilion Clinic
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.