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Open Abdominal Surgery clinical trials

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NCT ID: NCT06409156 Not yet recruiting - Clinical trials for Open Abdominal Surgery

EOIFP Block Versus OSTAP Block for Upper Abdominal Surgery

Start date: July 1, 2024
Phase: Early Phase 1
Study type: Interventional

The investigators propose a single-center, assessor blinded, randomized control trial to compare the efficacy of external oblique fascial plane (EOIFP) block versus Oblique Subcostal Transversus Abdominis Plane (OSTAP) block for patients undergoing open upper abdominal surgery at Cleveland Clinic Main Campus.

NCT ID: NCT06157138 Recruiting - Lung Ultrasound Clinical Trials

Observation of B-lines in Pulmonary Echography, During Open Abdominal Surgery

LUS-SURG
Start date: December 26, 2023
Phase:
Study type: Observational [Patient Registry]

There is no a reliable marker of intraoperative fluid excess or overload. The use of lung ultrasound in other settings, such as emergency room and critical care patients, helps us to determine if a patient has a condition of augmented intrathoracic fluid, that could be related to several circumstances, such as fluid overload, but also to heart failure, in example. Nevertheless, there is no information regarding the basal incidence of this finding, to ascertain if could be eventually used as a potential marker of fluid overload. This protocol looks for the incidence of the finding of B-Lines, which are related to fluid overload, in patients undergoing open abdominal surgery.

NCT ID: NCT06142526 Recruiting - Clinical trials for Open Abdominal Surgery

A Safety and Effectiveness Study of DividPro Film in Open Abdominal Surgery

Start date: December 12, 2023
Phase: N/A
Study type: Interventional

Abdominal adhesions frequently occur after surgery and may be one of the main reasons to cause discomfort, pain and related bowel movement symptoms. The goal of this clinical trial is to evaluate the safety of DividPro film and its potential effectiveness for reducing the incidence of abdominal adhesion. Treatment group will have DividPro film implantation right before the closure of surgical incision wound. Control group will have standard care without any anti-adhesion related products. In addition to adverse event assessment and safety lab tests, participants will accept abdominal ultrasound and quality of life questionnaire at each visit for effectiveness evaluation.

NCT ID: NCT04594174 Not yet recruiting - Clinical trials for Open Abdominal Surgery

Prediction Model of the Blood Pressure Response to the Administration of Fluids in Abdominal Surgery Using the Pram Method.

PREDICTPRAM
Start date: November 1, 2020
Phase:
Study type: Observational

Fluid therapy is considered a first-line therapy in resuscitation protocols for hemodynamically unstable patients. The administration of fluids usually translates into an increase in Cardiac Output. However, not all patients increase mean blood pressure after fluid administration. To determine if fluids the administration improves blood pressure, it is necessary to evaluate the dependence of preload, vasomotor tone, and left ventricular stroke volume. The aim of this study is to confirm the usefulness of dynamic elastance, cardiovascular impedance, cardiac cycle efficiency, and other hemodynamic parameters calculated with the PRAM method as predictors of blood pressure response after fluid administration in open abdominal surgery. This will allow us to make and evaluate a predictive model for the blood pressure response after fluid administration in open abdominal surgery.