Clinical Trials Logo

Abdominal Cancer clinical trials

View clinical trials related to Abdominal Cancer.

Filter by:

NCT ID: NCT06397573 Recruiting - Abdominal Cancer Clinical Trials

Ablative Stereotactic MR-Guided Adaptive Reirradiation

Start date: June 5, 2024
Phase: N/A
Study type: Interventional

This research study will enroll people who have cancer in their abdomen or pelvis that was treated previously with radiation therapy. The purpose of this research study is to test the safety and possible harms of treating tumors in these regions with another round of radiation therapy, called reirradiation or "reRT." The researchers want to find out what effects (good and bad) reRT has in people with cancer in the abdomen and pelvis.

NCT ID: NCT06384677 Completed - Abdominal Cancer Clinical Trials

Comparison of Postoperative Analgesia Methods in Patients Undergoing Major Intraabdominal Surgery

Start date: April 20, 2023
Phase: N/A
Study type: Interventional

This study aims to examine the effects of M-TAPA applied for postoperative analgesia in patients who had major intraabdominal surgery on the postoperative pain score, the change in the postoperative total opioid requirement and the side effects.

NCT ID: NCT06335238 Recruiting - Abdominal Cancer Clinical Trials

Radiotherapy Treatments for Neoplasms in the Abdominal-pelvic Region

Start date: February 22, 2018
Phase:
Study type: Observational

Evaluation of clinical and dosimetric aspects, tolerance, and effectiveness of abdominal-pelvic region radiotherapy treatments in patients undergoing radiotherapy for primary or secondary neoplasms localized in the tabdominal-pelvic region.

NCT ID: NCT06321874 Completed - Abdominal Cancer Clinical Trials

Effects of Oxygen After Abdominal Oncological Surgery

EPHIRAS
Start date: January 1, 2011
Phase: N/A
Study type: Interventional

The aims of the research is to determine whether a Hyperoxic intermittent stimuli protocol can increase reticulocyte counts, signififying a rise in EPO production, in patients undergoing abdominal surgery

NCT ID: NCT06316908 Completed - Cancer Pain Clinical Trials

Permanent Celiac Plexus Block: Comparison of Pain Score in Unilateral and Bilateral Posterior Percutaneous Approach

Start date: February 25, 2020
Phase: Phase 4
Study type: Interventional

The goal of this prospective, interventional, non-randomized study was to compare pain score in unilateral and bilateral posterior percutaneous neurolytic celiac plexus block (NCPB) in upper abdominal cancer patients. The main questions it aimed to answer are: 1. Whether unilateral or bilateral NCPB technique has a better pain relief 2. Was there any difference in terms of complication rates between these two approaches All participants were having upper abdominal cancer whether operated or non-operable cancer were given a unilateral or bilateral neurolytic celiac plexus block. Pain scores and adverse events at multiple time points post-procedure were recorded.

NCT ID: NCT06293391 Completed - Blood Pressure Clinical Trials

The Effect of Patient Position Changes on Advanced Cardiac Indices in Cancer Surgery

Start date: February 1, 2023
Phase:
Study type: Observational

Esophageal Doppler Monitoring (Deltex CardioQ Esophageal Doppler Monitor, ODM) is used to manage patients' fluid therapy by non-invasively measuring continuous cardiac output with an esophageal probe. The aim of this study was to compare the effects of patient position changes on cardiac indices and vital signs in patients who underwent major abdominal cancer surgery with laparoscopic and open surgery using ODM.

NCT ID: NCT06265948 Not yet recruiting - Abdominal Cancer Clinical Trials

Comparsion Between Intravenous Infusion of Ketofol and Inhalational Anasthetics in Abdominal Cancer Surgeries for Post Operative Analgesia

Start date: March 2024
Phase:
Study type: Observational

( post operative pain between intravenous infusion ketofol and standard inhalational general anesthesia in abdominal cancer surgeries )

NCT ID: NCT06144853 Not yet recruiting - Peritoneal Cancer Clinical Trials

The PIPAC PET Pilot Study, OPC-7

Start date: January 1, 2024
Phase:
Study type: Observational

The pilot study will investigate the use of repeated FDG-PET/CT scans in 16 patients with peritoneal metastasis originating from abdominal cancers treated with Pressurized Intraperitoneal Aerosol Chemotherapy. The study will focus on the potential of repeated FDG-PET/CT scans to evaluate the treatment as well as the feasibility in the patient group.

NCT ID: NCT05975619 Recruiting - Clinical trials for Head and Neck Cancer

A Prospective Imaging Study of the Integrated TrueBeam-HyperSight CBCT System

Start date: August 29, 2023
Phase: N/A
Study type: Interventional

Cone beam computed tomography (CBCT) images are routinely used in radiation treatment delivery workflows to align patients with the treatment beam. Conventional CBCT image quality is sufficient for this task but not good enough for other radiotherapy-related tasks, such as contouring anatomical structures and calculating radiation dose distributions. HyperSight is a new CBCT imaging system manufactured by Varian Medical Systems. The purpose of this study is to evaluate the integration of the HyperSight imaging system with Varian's TrueBeam radiotherapy system, a linear accelerator with a C-arm gantry that rotates about the patient to delivery radiation to the target malignancy. HyperSight CBCT images will be acquired prospectively from patients who are receiving radiation treatment. The HyperSight/TrueBeam system will be used for imaging only; patients receive their radiation treatment on cleared devices and no aspect of their treatment is affected by participation in the study. HyperSight images collected during the study will be evaluated for quality and utility and compared to conventional CBCT images as well as fan beam CT images used for treatment planning.

NCT ID: NCT05903430 Not yet recruiting - Lung Cancer Clinical Trials

A Feasibility Study of MRI Guided Stereotactic Ablative Radiotherapy (MIDSECTION)

MIDSECTION
Start date: May 2024
Phase:
Study type: Observational

To determine if the investigators are able to deliver highly focused, intense radiation to tumours in the abdominal region or chest cavity whilst limiting the dose to surrounding organs using a high field strength MR-Linac.