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Tumor clinical trials

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NCT ID: NCT02039232 Completed - Clinical trials for Degenerative Disc Disease

Safety and Efficacy of the CarboFix Pedicle Screw System

Start date: January 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of CarboFix' Pedicle Screw System in the lumbar spine.

NCT ID: NCT01946555 Completed - Neuropathic Pain Clinical Trials

Prospective Longitudinal Observational Study to Evaluate the Clinical Characteristics and Opioids Treatments in Patients With Breakthrough Cancer Pain

RER
Start date: September 2013
Phase: N/A
Study type: Observational

The BTP (Breakthrough pain)was defined as "a transient exacerbation of pain that occurs either spontaneously, or in relation to a specific predictable or unpredictable trigger, despite relatively stable and adequately controlled background pain". The BTP is a common clinical features in patients with cancer pain (BTcP: breakthrough cancer pain). The prevalence of BTcP is equal to 56%. Currently, the investigators tend to recognize the idiopathic/spontaneous or accident BTcP in the three sub-types: voluntary, non- voluntary and procedural. The diagnosis of BTCP is not always easy because in the cancer patient is normal to observe changes in the intensity of pain during the day, so it is necessary to differentiate slight fluctuations from the presence of real episodes of BTCP, for which is necessary to use a rescue treatment adjusted. In the study will be proposed the use of a diagnostic algorithm, present in the literature, to perform the diagnosis of BTCP. In the presence of BTCP, is important both a correct controlled background pain with major opioids, which can reduce the number and the intensity of the painful episodes, both implement an adjunctive therapy, called "rescue", to be administered at the time which takes over the painful episode using, in this case, an opioid greater.

NCT ID: NCT01919710 Completed - Cancer Clinical Trials

Safety and Efficacy Studies of rHSA/GCSF Fusion Protein For Injection to Treat Neutropenia

Start date: October 2012
Phase: Phase 1
Study type: Interventional

Safety and efficacy studies of rHSA/GCSF fusion protein for injection in treatment of neutropenia induced by chemotherapy of cancer patients.

NCT ID: NCT01874873 Completed - Tumor Clinical Trials

A Phase II Study of Anlotinib in MTC Patients

ALTN/MTC
Start date: April 2013
Phase: Phase 2
Study type: Interventional

Anlotibib (ALTN) is a kind of innovative medicines approved by State Food and Drug Administration(SFDA) which was researched by Jiangsu Chia-tai Tianqing Pharmaceutical Co., Ltd. ALTN is a kinase inhibitor of receptor tyrosine with multi-targets, especially for VEGFR2 and VEGFR3. It has the obvious resistance to new angiogenesis. The trial is to explore ALTN for the effectiveness of advanced medullary thyroid carcinoma and security.

NCT ID: NCT01867268 Recruiting - Tumor Clinical Trials

Effect of Acetazolamide & Position in CSF Leakage and Collection and Wound Dehiscence

Start date: October 2012
Phase: Phase 2
Study type: Interventional

- Purpose of study : to determine the preventive effect of acetazolamide administration, prone positioning, and the combination of both following the neurosurgical interventions in lumbosacral region for cerebrospinal fluid (CSF) leak, CSF collection and wound dehiscence. - Sample size: 144 - intervention groups: - Group A: Acetazolamide administration for 10 days - Group B: prone positioning for 10 days - Group C: Acetazolamide administration and prone positioning for 10 days - Group D: no intervention - Period of study: Autumn 2012 to the end of winter of 2015

NCT ID: NCT01851213 Completed - Cancer Clinical Trials

FoundationOne™ Test Registry Study

FMI Registry
Start date: March 2013
Phase: N/A
Study type: Observational [Patient Registry]

This study is a prospective, multicenter, observational study to characterize utilization patterns of the FoundationOne™ test by oncologists under conditions of routine clinical practice in the US. The study will also examine impact of test results on subsequent clinical decisions regarding choice of therapy. The planned duration of the study is at least 2 years with 1 year for patient recruitment and a minimum 1-year follow-up period for each patient. Any patient for whom the treating physician has ordered a FoundationOne™ test and a report is delivered is eligible for participation on the study. Eligible patients from participating sites will be enrolled sequentially during the 1-year enrollment period. Sites will be required to maintain an enrollment log of all patients for whom the FoundationOne™ test has been ordered and document patient disposition and reasons for non-participation. All treatment decisions and clinical assessment will be made at the discretion of the treating physician per usual care and are not mandated by study design or protocol. Informed consent will be obtained from eligible patients prior to study entry.

NCT ID: NCT01848431 Withdrawn - Tumor Clinical Trials

Randomized Study on the Effects of Moderate Anaemia in Free Microvascular Tissue Transfer

Start date: May 2013
Phase:
Study type: Observational

The evaluation of Perfusion of free flaps in patients with moderate anaemia and possible reduction of the transfusion threshold. - Trial with surgical intervention

NCT ID: NCT01846429 Terminated - Pain Clinical Trials

Oral Bicarbonate as Adjuvant for Pain Reduction in Patients With Tumor Related Pain

Start date: September 2013
Phase: Phase 1
Study type: Interventional

The purpose of this study is to: - Determine how well people tolerate sodium bicarbonate taken by mouth in higher doses than those usually given for heartburn. - Determine if sodium bicarbonate can reduce cancer-related pain.

NCT ID: NCT01773018 Completed - Tumor Clinical Trials

Phase I Study of the Volitinib (HMPL-504) in Patients With Advanced Solid Tumors

HMPL-504
Start date: February 2012
Phase: Phase 1
Study type: Interventional

Volitinib (HMPL-504) is a novel, highly potent and selective small molecule inhibitor of c-Met kinase. In preclinical studies, it demonstrated strong in vitro and in vivo activity against c-Met kinase and its downstream signaling targets and inhibited tumor cell growth. This first-in-human study is conducted to assess the maximum tolerated dose (MTD) and dose-limiting toxicity (DLT), to evaluate the pharmacokinetics, safety and preliminary anti-tumor activity of HMPL-504 at single doses and multiple doses.

NCT ID: NCT01739738 Withdrawn - Tumor Clinical Trials

The Impact of Ureteral Stents on Peristalsis

Start date: December 2012
Phase:
Study type: Observational

The purpose of the study is to investigate the impact of ureteral stents on the functioning of ureteral peristalsis (normal contractions in the ureteral organ muscle).