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Survival clinical trials

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NCT ID: NCT03291236 Recruiting - Clinical trials for Uterine Cervical Neoplasms

Survival Outcomes of Uterine Cervical Malignancies in Chinese Population

Start date: January 1, 2017
Phase: N/A
Study type: Observational

This study aims to determine survival outcomes (overall survival and progression-free survival) of primary malignancies of uterine cervix in China and relevant risk factors in a prospective cohort study.

NCT ID: NCT03247049 Completed - Clinical trials for Intracerebral Hemorrhage

Prognosis in Intracerebral Hemorrhage. The ICHCat Score in Primary Care.

ICHCat
Start date: July 27, 2015
Phase: N/A
Study type: Observational [Patient Registry]

The clinical evidence shows that patients with a first episode of intracerebral hemorrhage (ICH) are increasingly old and with greater comorbidity with a recognized impact over mortality. The prediction of the outcome of ICH is not only crucial in the emergin attention to identify those patients with favorable criteria that can benefit from possible treatments; but also after hospital discharge, in primary care where the prediction should facilitate the organization and management of a wide variety of resources: familiar, health and social welfare. Even though there are different scales that predict mortality, these are not sufficiently useful in choosing a treatment or do not provide sufficient data to the family to decide. Due to the characteristics of the population with ICH described in these works, it seems useful to propose a prognostic index (ICHCat) to identify the variables associated to its incidence and mortality and that, in addition, to make adjustments in the comparisons of the survival between different series of patients or different treatment modalities in primary care.

NCT ID: NCT03134807 Completed - Critical Illness Clinical Trials

The Very Old Intensive Care Patient: A Multinational Prospective Observation Study

VIP1
Start date: November 1, 2016
Phase:
Study type: Observational

- The primary aim is to document the incidence and short-term outcome of the elderly ICU patient (≥ 80 years) using a multicentre, multi national approach - The secondary aim is to investigate the properties of a simple frailty index in this cohort, and in particular if this is an instrument that can be used in resource and outcome prediction in this group - To create hypothesis for further studies, in particular on various outcome prediction

NCT ID: NCT03084809 Completed - Colorectal Cancer Clinical Trials

Chemotherapy Combined With CIK Treating Colon Cancer

Start date: May 6, 2012
Phase: Phase 4
Study type: Interventional

Cytokine-induced killer cells (CIK) is an auxiliary antitumor treatment. The investigators aim to evaluate the clinical efficacy of chemotherapy combined with CIK in the treatment of postoperative colorectal cancer patients. And to provide useful reference for the clinical application of CIK in colorectal cancer patients.

NCT ID: NCT02966769 Completed - Surgery Clinical Trials

N2 Lung Cancer Project: Neoadjuvant Treatment Followed Surgery Versus Chemoradiation

Start date: June 2016
Phase: N/A
Study type: Observational

The objective of this multicenter retrospective study is to compare overall survival in patients with stage IIIA-N2 NSCLC treated with neoadjuvant treatment and surgery versus definitive chemoradiation. Secondary objectives are to analyze disease-free survival, median survival, locoregional and distant relapses as well as mortality and toxicity related to treatment.

NCT ID: NCT02960061 Not yet recruiting - Survival Clinical Trials

Perioperative Chemotherapy Combined With HIPEC for High-risk Advanced Gastric Cancer

HIPEC
Start date: November 2016
Phase: Phase 3
Study type: Interventional

The investigators intend to conduct a randomized controlled study to find if combining HIPEC (hyperthermic intraperitoneal perfusion chemotherapy) with post-neoadjuvant chemotherapy D2 resection could improve survival for patients with advanced gastric cancer, while comparing with the traditional approach of D2 resection after neoadjuvant chemotherapy.

NCT ID: NCT02660411 Completed - Neoplasms Clinical Trials

Impact of Anesthesia Maintenance Methods on Long-term Survival

Start date: April 1, 2015
Phase: N/A
Study type: Interventional

Surgery is one of the major treatment methods for patients with malignant tumor. And, alone with the ageing process, more and more elderly patients undergo surgery for malignant tumor. Evidence emerges that choice of anesthetics, i.e., either inhalational or intravenous anesthetics, may influence the outcome of elderly patients undergoing cancer surgery. From the point of view of immune function after surgery and invasiveness of malignant tumor cells, propofol intravenous anesthesia may be superior to inhalational anesthesia. However, the clinical significance of these effects remains unclear. Retrospective studies indicated that use of propofol intravenous anesthesia was associated higher long-term survival rate. Prospective studies exploring the effect of anesthetic choice on long-term survival in cancer surgery patients are urgently needed.

NCT ID: NCT01952184 Completed - Survival Clinical Trials

Oocyte Survival After Vitrification in an Open or Closed Device With Closed Storage.

Start date: September 2013
Phase: N/A
Study type: Interventional

The survival rate (and embryo quality) of donor oocytes with two commercially available devices.

NCT ID: NCT01843985 Not yet recruiting - Survival Clinical Trials

Observational Study of Survival Outcomes of Stage IV Cancer Patients

Start date: June 2013
Phase: N/A
Study type: Observational

Patients diagnosed with Stage IV cancer (solid tumors only) are evaluated to determine whether they are candidates for traditional chemotherapy. If eligible, patients are offered traditional chemotherapy, low-dose chemotherapy, or palliative care. If ineligible, patients are offered low-dose chemotherapy or palliative care. Patients will be monitored for 5 years and survival data recorded.

NCT ID: NCT01835821 Active, not recruiting - Survival Clinical Trials

Clinical Study of Porcelain-fused and IPS e.Max CAD Crowns

Start date: March 2010
Phase: N/A
Study type: Interventional

This clinical study has the objective to compare the longevity and the clinical behaviour (CDA Index, soft tissue behavior, success and survival rates) of single cemented ceramic crowns made with shaded zirconia (NobelProceraTM Shaded Zirconia) and NobelProceraTM full contour crowns IPS e.max CAD lithium disilicate on molars.