search

Active clinical trials for "Pancreatic Neoplasms"

Results 641-650 of 2501

Stereotactic Body Radiotherapy Dose Escalation in Pancreatic Cancer

Pancreatic Cancer

This study is to determine the maximum tolerated dose (MTD) of five fraction stereotactic radiotherapy (SBRT) in pancreatic cancer.

Active12 enrollment criteria

Genetic Testing for Breast, Ovarian, Pancreatic, and Prostate Cancers

Breast CancerOvarian Cancer2 more

This study is evaluating the effect of two pre-test education methods on participants interested in genetic testing for hereditary cancer risk.

Active10 enrollment criteria

Effects on Quality of Life With Zinc Supplementation in Patients With Gastrointestinal Cancer

Gastric CarcinomaLiver and Intrahepatic Bile Duct Carcinoma2 more

This randomized study examines how well zinc works in improving quality of life in patients with gastrointestinal cancer that cannot be removed by surgery who are receiving chemotherapy. Zinc may help to improve patient's quality of life by preventing zinc deficiency.

Active5 enrollment criteria

Telotristat Ethyl to Promote Weight Stability in Patients With Advanced Stage Pancreatic Cancer...

Locally Advanced Unresectable Pancreatic AdenocarcinomaMetastatic Pancreatic Adenocarcinoma3 more

This phase II trial studies how well telotristat ethyl works in promoting weight stability in patients with pancreatic adenocarcinoma that has come back and spread to other places in the body. Telotristat ethyl may decrease bowel movements which may make patients gain weight. Stabilizing weight may help patients tolerate chemotherapy better and improve longevity.

Active45 enrollment criteria

Acupuncture for the Management of Postoperative Pain in Patients With Pancreatic or Colorectal Cancer...

Resectable Colorectal CarcinomaResectable Digestive System Carcinoma1 more

This trial investigates how well acupuncture works for the management of pain after surgery in patients having open colorectal or pancreatic surgery. Acupuncture may help to reduce postoperative symptoms including pain. This study may help researchers learn if acupuncture reduces after-surgery side effects and improves recovery.

Active11 enrollment criteria

GENetic Education Risk Assessment and TEsting Study

Candidates for Hereditary Pancreatic Cancer Testing

The goal of the GENERATE Study is to improve genetic testing and cancer prevention in family members of pancreatic cancer patients who may have genetic mutations (inherited changes). The study will measure how different methods of genetic education increase the rate of genetic testing in these families. This is an investigational study to measure the effects of two methods of genetic education. Participants may elect to undergo genetic testing as part of the study and will be asked to provide a saliva sample via a saliva-testing kit. The genetic testing done in this study is FDA approved and will be processed in a Clinical Laboratory Improvement Amendments (CLIA) certified laboratory. Up to 1,000 participants will be enrolled in this study.

Active15 enrollment criteria

In Vivo PARP-1 Expression With 18F-FTT PET/CT in Pancreatic Cancer

Pancreatic Cancer

The investigators plan to enroll 30 evaluable patients with (1) a histological diagnosis of advanced pancreatic ductal adenocarcinoma who have demonstrated at least stable disease following ≥16 weeks of treatment with platinum-based chemotherapy and (2) who have signed consent to participate in a clinical trial that contains PARP inhibitor therapy and are anticipated to receive this treatment or (3) will receive PARP inhibitor therapy as part of their clinical care. A pre-treatment 18F-FluorThanatrace ([18F]FTT) positron emission tomography/computed tomography (PET/CT) scan will be done prior to the start of treatment with a PARP inhibitor. PET/CT imaging will be used to evaluate PARP-1 expression in sites of pancreatic cancer using the investigational radiotracer [18F]FTT. This is an observational study in that [18F]FTT PET/CT will not be used to direct treatment decisions. While patients and referring physicians will not be blinded to the [18F]FTT PET/CT results, treatment decisions will be made by the treating physicians based upon clinical criteria. Patients will undergo approximately 60 minutes of dynamic scanning starting at the time of injection of [18F]FTT. This procedure will be followed by a skull base to mid-thigh scan, starting at approximately 60 minutes post injection. PET/CT imaging sessions will include an injection of approximately 10 mCi (approximate range for most studies is anticipated to be 8-12 mCi) of [18F]FTT. Data will be collected to evaluate uptake of [18F]FTT in sites of pancreatic cancer, which will be compared with PARP-1 expression in tissue, when available. All 30 evaluable patients are expected to start PARP inhibitor therapy following the [18F]FTT PET/CT scan. It is expected that due to patient preference and time considerations, approximately 24 patients (80%) will also undergo a second (optional) scan that will be performed approximately 3 weeks (± 1 week) after therapy has started. The second scan is obtained to evaluate whether the PARP inhibitor therapy decreases [18F]FTT uptake, which would suggest PARP blocking by the therapy.

Active8 enrollment criteria

Walking for Recovery From Surgery in Improving Quality of Life in Older Adults With Lung or Gastrointestinal...

Adult Liver CarcinomaCaregiver4 more

This pilot clinical trial studies how well Walking for Recovery from Surgery works in improving quality of life in older adults with lung or gastrointestinal cancer and their family caregivers. A walking program, such as Walking for Recovery from Surgery may help support overall well-being as a caregiver, and may help improve family member or friend's recovery from surgery.

Active13 enrollment criteria

Evaluation of an Adapted Physical Activity Program in Patients With Unresectable Pancreatic Cancer...

Unresectable Locally Advanced CancerMetastatic Pancreatic Cancer

Adapted Physical Activity (APA) program may provide an opportunity to improve symptoms for patients with unresectable pancreatic cancer. Thereby, it is proposed to conduct an open trial to assess effects of the APA program in such population

Active17 enrollment criteria

Preoperative Optimisation of Modifiable Risk Factors in Surgery of the Pancreas

PrehabilitationPancreas Cancer2 more

The goal of this stepped-wedge randomized controlled trial is to investigate whether implementation of a best practice program for preoperative optimisation (prehabilitation program) with a focus on screening, assessment, and intervention of 8 potentially (partly) modifiable risk factors in patients with (suspected) pancreatic cancer will improve outcome. The main questions it will aim to answer are: Does a prehabilitation program improve the time to functional recovery after pancreatic surgery? Does a prehabilitation program lead to a reduction in the Comprehensive Complication Index after pancreatic surgery?

Not yet recruiting3 enrollment criteria
1...646566...251

Need Help? Contact our team!


We'll reach out to this number within 24 hrs