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NCT ID: NCT02531841 Recruiting - Clinical trials for Diffuse Large B-cell-lymphoma

High-dose Chemotherapy and ASCT or Consolidating Conventional Chemotherapy in Primary CNS Lymphoma

MATRix
Start date: July 2014
Phase: Phase 3
Study type: Interventional

In the presently planned multicentre Phase III trial the two therapies will be compared: Patients will be randomized after intensified induction treatment with 4 cycles rituximab, methotrexate, cytarabine and thiotepa (MATRix) between first-line high-dose chemotherapy against conventional consolidating therapy with 2 cycles of conventional chemotherapy with R-DeVIC (rituximab, dexamethasone, etoposide, ifosfamide, carboplatin).

NCT ID: NCT02530229 Recruiting - Septic Arthritis Clinical Trials

Arthrocentesis Study

Start date: November 2014
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to analyze pre- and intra-operative joint aspirates of native joints and joints with suspicion of periprosthetic joint infection (PJI) of the hip, knee and shoulder acquired in clinical routine. Joint aspirates are then analyzed with new diagnostic methods (microcalorimetry, PCR, alpha-defensin, etc.). Diagnostic speed and accuracy of these methods is compared to standard diagnostic methods in clinical routine, such as blood cultures of joint aspirates, cell count/differential, intra-operative tissue culture and histology and sonication.

NCT ID: NCT02528955 Recruiting - Clinical trials for Cancer of Head and Neck

De-Intensification Radiotherapy Postoperative Head Neck

DIREKHT
Start date: October 2014
Phase: Phase 2
Study type: Interventional

In patients with squamous cell carcinoma of the oral cavity, the oropharynx and larynx with >= pT3 and or pN+ postoperative radio - or radiochemotherapy is the standard of care. Postoperative radiochemotherapy is indicated in patients with multiple lymph node metastasis, lymph node metastasis with extracapsular spread and or R1/2 resection. Locoregional control rates are over 80% after surgery and radio(chemo)therapy. But many patients suffer from therapy-related long-term side-effects, like xerostomia, dysphagia, fibrosis, trismus etc. The aim of this study is to investigate if depending on primary tumor stage, quality of resection ( resection margin) and number of lymph node metastasis and performed neck dissection an adapted de-intensified dose- and target volume concept may be performed without reducing locoregional-control but with reducing radiotherapy-related side-effects.

NCT ID: NCT02526264 Recruiting - Colorectal Cancer Clinical Trials

Evaluation of Quality of Life and Period of Hospitalization by Education

STELLA
Start date: November 24, 2015
Phase: N/A
Study type: Interventional

Patients with colorectal cancer prior to stoma surgery are randomized to different preoperative education programs: (a) specific preoperative education, (b) standard preoperative education. Outcome measures are quality of life, period of hospitalization and complication rates.

NCT ID: NCT02520986 Recruiting - Clinical trials for Condylomata Acuminata

Carbon Dioxide Laser vs. Electrocoagulation for the Therapy of Condyloma

Start date: December 2016
Phase: N/A
Study type: Interventional

In a randomized clinical trial of 114 women undergoing Treatment for condyloma acuminata, two surgical methods, the carbon dioxide laser Ablation and the excision by electrocoagulation, will be compared. The primary outcome of the study is the cosmetic result judged by the Patient 6 weeks after Treatment using a 11-step visual analogue scale (VAS), secondary outcomes are intervention time, operative complications, subjects and users satisfaction, postoperative pain and recurrence of genital warts.

NCT ID: NCT02519582 Recruiting - Colorectal Cancer Clinical Trials

Drug Trial to Investigate the Safety and Efficacy of Niclosamide Tablets in Patients With Metastases of a Colorectal Cancer Progressing After Therapy

Nikolo
Start date: August 2015
Phase: Phase 2
Study type: Interventional

Phase II trial evaluating the safety and efficacy of oral appliqued niclosamide in patients who are progressive with metachronous or synchronous metastases of colorectal cancer among the previous therapy (Nikolo). Monocentric open-label clinical trial of phase II. All patients received 2 g p.o. niclosamide daily until progression (according to RECIST) or unacceptable toxicity or discontinuation of study for other reasons.

NCT ID: NCT02517827 Recruiting - Clinical trials for Peripheral Artery Disease

Percutaneous Intervention Versus Surgery in the Treatment of Common Femoral Artery Lesions

PESTO-AFC
Start date: August 1, 2017
Phase: N/A
Study type: Interventional

The endovascular therapy prevailed in nearly all regions of peripheral artery disease over open surgery techniques. However, in treatment of the common femoral artery vascular surgery is still the gold standard of therapy. One-year patency rates are between 90% and 95%. Today, only in selected cases an endovascular procedure for common femoral artery diseases is recommended. The primary objective of this study is to compare the performance of directional atherectomy and drug-coated balloon angioplasty over vascular surgery in common femoral artery lesions in a prospective, multi-center, randomized clinical trial.

NCT ID: NCT02516540 Recruiting - Clinical trials for Hereditary Breast and Ovarian Cancer

Efficacy of Lifestyle Intervention in BRCA1/2 Mutation Carriers

LIBRE-2
Start date: March 2015
Phase: N/A
Study type: Interventional

The hypothesis of this 3 year, prospective randomized multicenter efficacy trial is that a structured life-style intervention program with exercise training and mediterranean diet is effective regarding increased adherence to a mediterranean diet, reduction of body mass index, and increase of physical fitness.

NCT ID: NCT02513537 Recruiting - Clinical trials for Postoperative Delirium

Postoperative Delirium - European Society of Anaesthesiology Survey

Start date: August 2015
Phase:
Study type: Observational

The ESA is currently preparing a guideline on the management of postoperative delirium (POD), which attempts to reduce the impact of postoperative delirium and provide recommendations for prevention, diagnostics and treatment of delirium outside the intensive care unit. The guidelines are going to be published during 2015. While the guideline provides recommendations for daily practice, assessment of current practice and knowledge is of utmost importance, because the implementation and the measurement of a change in clinical practice will be dependent on these measurements. This Survey has been approved by the Scientific and Research Committees of the European Society of Anaesthesiology (ESA), the Media Committee of the ESA, as well as the institutional ethical committee of Charité - Universitätsmedizin Berlin.

NCT ID: NCT02512328 Recruiting - Clinical trials for Gastrointestinal Neoplasms

Improvement of Colonoscopy Preparation by New Media (APP)

PERICLESAPPI
Start date: March 2015
Phase: Phase 1
Study type: Interventional

Feasibility of an newly programmed offline application for smartphones (SPA, APP) for colonoscopy preparation offering a 5 day guidance prior colonoscopy containing dietary- and behavioral recommendation.