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Recurrence clinical trials

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NCT ID: NCT03846661 Completed - Clinical trials for Postoperative Complications

Nationwide Long-term Outcome Surveillance of Physiomesh® vs. Other Meshes in Laparoscopic Incisional Hernia Repair

Start date: January 1, 2010
Phase: N/A
Study type: Interventional

The primary aim of the present study was to show how a national clinical register combined with other nationwide administrative registers may serve as a tool for pre- and post-marketing evaluation of new mesh and mesh fixation products for hernia surgery, using Physiomesh® versus other meshes designed for laparoscopic hernia repair as an example.

NCT ID: NCT03841435 Completed - Clinical trials for Recurrent Diffuse Intrinsic Pontine Glioma

Hypofractionated Radiotherapy for Recurrent DIPG

Start date: January 31, 2018
Phase: N/A
Study type: Interventional

This study evaluates the feasibility of hypofractionated radiotherapy (RT) in the palliative treatment of recurrent diffuse intrinsic pontine glioma (DIPG). Participants will receive 15 Gy in 3 fractions as opposed to the standard 20 Gy in 10 fractions.

NCT ID: NCT03841266 Completed - Clinical trials for Relationship and Consistency Analysis

Recurrence Risk Evaluation by 21-gene Detection

Start date: January 1, 2019
Phase:
Study type: Observational

Breast cancer patients with early breast cancer were enrolled according to the inclusion criteria. Baseline characteristics were recorded from medical record system. Recurrence score were obtained by 21-gene detection kits from different biological companies. Relationship between recurrence score and the prognosis was explored. Meanwhile, the investigators analyzed the consistency of the results obtained from various 21-gene test kits and immunohistochemistry detection.

NCT ID: NCT03833960 Completed - Clinical trials for Sentinel Lymph Node Biopsy

SLNB After Neoadjuvant Treatment in Node Positive Patients

Start date: May 2016
Phase:
Study type: Observational

From May 2016 till May 2018 all breast cancer patients with operable disease submitted to surgery after neoadjuvant treatment would be divided in four groups considering initially clinical axillary stage, axillary procedure that was done, axillary response to preoperative systemic treatment and pathological axillary stage. In first postoperative year all patients will be monitored for appearance of locoregional and distant recurrence.

NCT ID: NCT03823274 Completed - Ischemic Stroke Clinical Trials

Multi-center, Prospective, Cohort Study to Evaluate the Relationship of Stroke Recurrence and Anti-platelet Resistance in Ischemic Stroke Patients

Start date: April 1, 2019
Phase:
Study type: Observational [Patient Registry]

This cohort study will evaluate the relatiobship of stroke recurrence and anti-platelet resistance in ischemic stroke patients

NCT ID: NCT03816553 Completed - Clinical trials for Recurrent Cervical Carcinoma

SHR-1210 in Combination With Apatinib in Patients With Metastatic, Persistent, or Recurrent Cervical Cancer

Start date: January 19, 2019
Phase: Phase 2
Study type: Interventional

The purpose of this study is to explore the efficacy and safety of SHR-1210 in combination with apatinib in treating patients with metastatic, persistent, or recurrent cervical cancer.

NCT ID: NCT03815357 Completed - Clinical trials for Primary Immunodeficiency

What is the Incidence of an Immune Disorder in Children With Invasive Pneumococcal Disease (IPD)?

Start date: January 31, 2017
Phase:
Study type: Observational

This is a multicentre prospective audit to determine the incidence of immunodeficiency in children with IPD. Aims and/or research question of the project 1. To determine the incidence of primary immunodeficiency in children >2 years who present with IPD 2. To determine the types of immunodeficiency associated with IPD in children

NCT ID: NCT03813147 Completed - Clinical trials for Refractory Acute Myeloid Leukemia

Pevonedistat, Azacitidine, Fludarabine Phosphate, and Cytarabine in Treating Patients With Relapsed or Refractory Acute Myeloid Leukemia or Myelodysplastic Syndrome

Start date: May 17, 2019
Phase: Phase 1
Study type: Interventional

This phase I trial studies the side effects and how well pevonedistat, azacitidine, fludarabine phosphate, and cytarabine work in treating patients with acute myeloid leukemia or myelodysplastic syndrome that has come back (relapsed) or has not responded to treatment (refractory). Pevonedistat may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Chemotherapy drugs, such as azacitidine, fludarabine phosphate, and cytarabine, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving more than one drug (combination chemotherapy) and pevonedistat may work better in treating patients with acute myeloid leukemia or myelodysplastic syndrome.

NCT ID: NCT03810924 Completed - Clinical trials for Alcohol Use Disorder

Stress-related Predictor Profiles in Human Addiction

Start date: July 1, 2019
Phase: N/A
Study type: Interventional

Long-term aim is the definition of a setup of mobile sensors and their integration in a mobile infrastructure that allows the prediction of stress related alcohol intake in an ambulatory setting. Here, we aim to identify stress- and alcohol cue-related physiological markers in a lab experiment to assess interactions between acute psychological vs. physical stress exposure and alcohol cue-exposure regarding their effects on measures relevant for the development and maintenance of Alcohol Use Disorder (AUD). Further, we aim to identify neural correlates in brain circuits of motivational, cognitive, and affective processing. In addition to applying established stress-related markers, we will integrate innovative sensor-based measures.

NCT ID: NCT03808818 Completed - Malignant Neoplasm Clinical Trials

Implementing a Virtual Tobacco Treatment for Cancer Patients in Community Oncology Practices

Start date: August 1, 2019
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well smoking cessation treatment plans work in tobacco-dependent cancer patients when delivered virtually as part of their cancer care in community oncology practices. Virtual information and counseling sessions may help cancer patients quit smoking.