Clinical Trials Logo

Neoplasms clinical trials

View clinical trials related to Neoplasms.

Filter by:

NCT ID: NCT03184350 Recruiting - Clinical trials for Uterine Cervical Neoplasms

Adjuvant Protontherapy of Cervical and Endometrial Carcinomas

APROVE
Start date: June 2017
Phase: N/A
Study type: Interventional

The APROVE study is a prospective single-center single-arm phase-II study. Patients with cervical or endometrial cancer after surgical resection who have an indication for postoperative pelvic radiotherapy will be treated with proton therapy instead of the commonly used photon radiation. A total of 25 patients will be included in this trial. Patients will receive a dose of 45-50.4 Gray in 1.8 Gray fractions 5-6 times per week using active raster-scanning pencil beam proton radiation. Platinum-based chemotherapy can be administered if indicated. The primary endpoint of the study is the evaluation of safety and treatment tolerability of pelvic radiation using protons defined as the lack of any CTC AE Grade 3 or 4 toxicity. Secondary endpoints are clinical symptoms and toxicity, quality of life and progression-free survival. The aim is to explore the potential of proton therapy as a new method for adjuvant pelvic radiotherapy to decrease the dose to the bowel, rectum and bladder thus reducing acute and chronic toxicity and improving quality of life.

NCT ID: NCT03184038 Recruiting - Clinical trials for Metastatic Malignant Solid Neoplasm

Neurocognition in Patients With Multiple Brain Metastases Treated With Radiosurgery

Start date: February 21, 2017
Phase: Phase 2
Study type: Interventional

This phase II trial studies the neurological function in patients with multiple brain metastases undergoing stereotactic radiosurgery (SRS) or stereotactic body radiation therapy (SBRT). Stereotactic body radiation therapy uses special equipment to position a patient and deliver radiation to tumors with high precision. This method can kill tumor cells with fewer doses over a shorter period and cause less damage to normal tissue. Assessment of neurocognitive function may help show that SRS preserves neurological function in patients with multiple brain metastases better than SBRT.

NCT ID: NCT03183271 Completed - Clinical trials for Neuroendocrine Tumors

Proton Boost for Locally Advanced HEAD AND NECK TUMORS

Start date: July 16, 2012
Phase: N/A
Study type: Interventional

The aim of this research project is to test the local response and the acute toxicity (which can be observed within 90 days).

NCT ID: NCT03182673 Terminated - Solid Tumor Clinical Trials

The Study of SHR7390 in Combination With SHR-1210 and SHR3162 in Patients With Advanced Solid Tumors

Start date: July 24, 2017
Phase: Phase 1
Study type: Interventional

The study consists of the two parts, the first one is SHR7390 combined with SHR-1210, the second one is SHR7390 combined with SHR-1210 and SHR3162. Two parts of the study are separately to assess the safety and tolerability, to define dose limiting toxicity(DLT) and maximum tolerated dose (MTD),to evaluate the pharmacokinetics ,to assess the antitumor activity in patients with advanced solid tumors preliminarily and to recommend reasonable dosage regimen of SHR7390 for the follow-up clinical trial.

NCT ID: NCT03182257 Terminated - Solid Tumor Clinical Trials

Study of ONO-7579 in Patients With Advanced Solid Tumors/ NTRK Gene Fusion Positive Advanced Solid Tumors

ONTRK
Start date: July 12, 2017
Phase: Phase 1
Study type: Interventional

This study will determine the safety and maximum tolerated dose of ONO-7579 in patients with advanced solid tumors, and evaluate efficacy of ONO-7579 in patients with advanced solid tumors harboring NTRK gene fusions.

NCT ID: NCT03181997 Completed - Clinical trials for Aortic Valve Stenosis

Outcomes of Transcatheter Aortic Valve Implantation in Oncology Patients With Severe Aortic Stenosis

TOP-AS
Start date: January 1, 2017
Phase:
Study type: Observational [Patient Registry]

As for today, transcatheter aortic valve implantation (TAVI) is indicated only in symptomatic patients with severe aortic stenosis (AS) at high surgical risk. As cancer therapy improves, some AS patients suffering active malignancy (including advanced metastatic diseases) may be more endangered by their untreated valvular disease than their oncological disease. Among these patients, TAVI may be indicated before cancer related surgery or cardiotoxic anti-cancer therapy in order to achieve better anti-cancer therapy outcomes. Individualized life expectancy assumptions should be evaluated by the heart team in the clinical decision-making process as an essential factor in weighing the risk-benefit ratio for oncologic patients undergoing TAVI. A multicenter, international TAVI in Oncology Patients with AS (TOP-AS) registry was designed to collect data on patients with an active malignancy and severe AS undergoing TAVI. The aim of the study is to evaluate the outcomes, benefits and risks of oncology patients undergoing TAVI, mainly the patients' survival and cause of death and also the interactions between the valvular and the oncologic conditions.

NCT ID: NCT03180970 Not yet recruiting - Clinical trials for Image Quality of Early Esophageal Squamous Neoplasia

Different Lugol's Solution Concentration for Image Quality of Esophageal Lesions in Chromoendoscopy With Iodine Staining

Start date: June 2017
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess whether lower Lugol's solution concentration can perceive the same image quality of early esophageal squamous neoplasia.

NCT ID: NCT03179436 Completed - Clinical trials for Advanced Solid Tumors

Study of Quavonlimab (MK-1308) in Combination With Pembrolizumab (MK-3475) in Advanced Solid Tumors (MK-1308-001)

Start date: July 2, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

This study will assess the safety, tolerability, pharmacokinetics (PK), and preliminary efficacy of escalating doses of quavonlimab when used in combination with pembrolizumab in participants with advanced solid tumors.

NCT ID: NCT03177928 Not yet recruiting - Clinical trials for Myeloproliferative Neoplasm

Cardiac Changes in Myeloproliferative Neoplasms

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

Myeloproliferative neoplasms are heterogeneous group of clonal hematopoietic stem cell neoplasms with excessive proliferation of one or more of the erythroid, megakaryocytic, or myeloid lineages and relatively normal maturation resulting in increased numbers of red cells, platelets, and/or granulocytes in the peripheral blood. Constitutive tyrosine kinase activation appears to be a common pathogenetic mechanism.

NCT ID: NCT03177681 Withdrawn - Clinical trials for Malignant Neoplasms of Independent (Primary) Multiple Sites

The Effect of Yogurt in Cancer Patient With Moderate Gastrointestinal (GI) Symptoms

Start date: March 1, 2022
Phase: N/A
Study type: Interventional

The goal of this clinical research study is to learn if probiotics found in yogurt can help to decrease gastrointestinal (GI) symptoms in cancer patients. Probiotics are live bacteria and yeast that help with many of our functions and may help digestive problems. Researchers also want to learn if the bacteria in your stool change as your symptoms change while eating yogurt.