Clinical Trials Logo

Disease-Free Survival clinical trials

View clinical trials related to Disease-Free Survival.

Filter by:
  • Recruiting  
  • Page 1

NCT ID: NCT05436561 Recruiting - Clinical trials for Disease-free Survival

Reduced MBF Regimen for Patients >=55 Years With Myeloid Malignancies

Start date: June 1, 2022
Phase: Phase 2
Study type: Interventional

In this multiple-center phase II study, the aim is to evaluate the clinical outcome of reduced intensity conditioning regimen with fludarabine (150mg/m2), busulfan (6.4mg/kg) and melphalan (100mg/m2) in patients with myeloid malignancies including AML, MDS and CMML >=55 years.

NCT ID: NCT04245410 Recruiting - Overall Survival Clinical Trials

Surgical Treatment of Pancreatic Metastases From Renal Cell Carcinoma

PANMEKID
Start date: March 1, 2019
Phase:
Study type: Observational

Pancreatic metastases are a rare entity. In cases of metastatic renal carcinoma (RCC) it can present as isolated pancreatic metastasis, considering the possibility of surgical resection. Goals: - Define survival after resection of pancreatic cancer metastases renal in a wide range of our country. - Identify predictive survival factors Methods: Retrospective multicenter study in which cases of pancreatic resection due to renal cancer metastases.

NCT ID: NCT04138992 Recruiting - Clinical trials for Disease Free Survival

A Study on the Efficacy and Safety of Bevacizumab in Untreated Patients With Locally Advanced Cervical Cancer

Start date: August 1, 2020
Phase: Phase 2/Phase 3
Study type: Interventional

To verify the clinical efficacy and safety of bevacizumab in treating local advanced cervical cancer, present study was designed to investigate the clinical results of bevacizumab combined with concurrent chemoradiotherapy (CCRT) in local advanced cervical cancer

NCT ID: NCT03967457 Recruiting - Quality of Life Clinical Trials

Comprehensive Study on the Quality of Life in Cervical Cancer Patients

Start date: June 19, 2019
Phase:
Study type: Observational

This is prospective cohort study. All the patients with primary cervical cancer in the future three years in Peking Union Medical College Hospital will be included in this study. Before and after the major therapy (including at least radical hysterectomy and/or radiotherapy), the patients accept (1) the questionnaires survey about quality of life; (2) urodynamic testing; (3) rectum dynamics testing and (4) ovarian reserve function. The survival outcomes (disease-free survival and overall survival) will be supplemented as secondary objectives.

NCT ID: NCT03504449 Recruiting - Clinical trials for Disease-free Survival

Surgery Without Neoadjuvant Chemoradiotherapy Compared With Neoadjuvant Chemoradiotherapy for Rectal Cancer With Negative Circumferential Resection Margin Based on MRI Assessment, a Perspective Multicenter Randomized Controlled Trial

SCRM-01
Start date: December 1, 2016
Phase: N/A
Study type: Interventional

For now, neoadjuvant chemoradiotherapy is routinely performed for T3N1-2M0 rectal cancer. However, there are lots of complications following neoadjuvant chemoradiotherapy, such as Wound-related complications, anastomotic leakage, anastomotic stenosis, sexual dysfunction, testicular or ovary failure. Patients undergoing resection for rectal cancer had low rates of local recurrence and long disease-free survival regardless of whether an APR, CAA or low AR was performed. The main purpose of preoperative radiotherapy is to lower the local recurrence. For the T3N1-2M0 rectal cancer with negative circumferential resection margin based on MRI assessment, we suppose might not necessary to receive neoadjuvant chemoradiotherapy, for operation can achieve the negative circumferential resection margin.

NCT ID: NCT03038256 Recruiting - Rectal Cancer Clinical Trials

Effect of Concurrent Capecitabine-based Long-term Radiotherapy Followed by XELOX Plus TME in Patients With High Risk Rectal Cancer: a Multi-centers, Randomized Controlled, Open-Label Trial

EXPLORE
Start date: January 31, 2018
Phase: Phase 2
Study type: Interventional

The purpose of this study was to evaluate the effect of concurrent capecitabine-based long-term radiotherapy followed by 4 cycles XELOX pre- a delayed TME compared with 6 cycles XELOX post- a Regular Timing TME in patients with high-risk rectal cancer defined by MRI.