Survival

15

Review clinical trials related to Survival. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Long-term Follow-up of Dexmedetomidine-esketamine and tDCS for Neurocognitive Complications After Surgery

Neurocognitive complications, mainly delirium and neurocognitive disorders, are common cerebral complications in older patients after surgery and associated with worse long-term outcomes. An ongoing 2×2 factorial trial conducted by the investigators plan to test the effects of perioperative dexmedetomidine-esketamine combination and transcranial direct current stimulation (tDCS) on postoperative neurocognitive complications in older patients. This long-term follow-up of the ongoing trial aims to investigate the effects of perioperative dexmedetomidine-esketamine combination and tDCS on long-term outcomes in older patients after noncardiac surgery.

Participants needed: 1,160
Trial details
Phase: Phase 4Age: 65-90Biological sex: AllType: InterventionalSponsor: Peking University First HospitalUpdated: May 12, 2026Locations: 6
Eligibility criteria

Aged 65 to 90 years; [+3]

Preoperative inability to communicate due to coma, severe dementia, endstage dis... [+8]

Status: Recruiting

Brentuximab Vedotin for Newly Diagnosed cHL in Chinese CAYA Based on PET/CT Assessment

Generally, pediatric patients tolerate acute toxicities but are vulnerable to late effects. Thus, increasing chemotherapy intensity to achieve more rapid complete early response to limit radiation therapy is worth testing. In this CCCG-HL-2024 study, Brentuximab vedotin (Bv) was used to replace VCR and bleomycin in the ABVE-PC regimen in the previous CCCG-HD-2018 study, respectively, to form a Bv-AEPC regimen for the treatment of newly diagnosed classic Hodgkin lymphoma (cHL) in children, adolescents and young adults. On the premise of maintaining a 4-year event free survival (EFS)\>90% in the low-, intermediate-and high-risk groups, increase the early assessment complete response rate (the overall early complete response rate increased by 20%, that is, from 54.0% to 74.0%) to further reduce the proportion of children receiving radiotherapy to benefit them.

Participants needed: 96
Trial details
Phase: Phase 2, Phase 3Age: 2-35Biological sex: AllType: InterventionalSponsor: Children's Cancer Group, ChinaUpdated: Mar 19, 2026Locations: 1
Eligibility criteria

Ages >=2~<35 years at the time of enrollment; [+3]

Patients with nodular lymphocyte-predominant HL; [+3]

Status: Not yet recruiting

Changes in Body Composition of Patients With Obesity Related Tumors and Their Impact on Clinical Outcomes: a Multicenter Prospective Cohort Study

Over the past 20 years, China's obesity rates have surged, increasing cancer burden. Obesity links to 13 cancers via metabolic effects of visceral fat and insulin resistance, while sarcopenic obesity (BMI-independent) may worsen outcomes. Traditional BMI lacks precision; advanced methods (e.g., BIA/CT) are needed. Existing studies show inconsistent results, possibly due to heterogeneity. This multicenter prospective cohort study uses imaging to assess body composition changes (fat/muscle) in obesity-related tumors and their impact on survival, recurrence, and quality of life, and explore the underlying mechanism.

Participants needed: 6,743
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Peking Union Medical College HospitalUpdated: Sep 8, 2025Locations: 1
Eligibility criteria

Age ≥18 years, regardless of gender. [+2]

Patients with concurrent non-obesity-related malignancies. [+2]

Status: Recruiting

Anesthesia Induced Brain Cancer Survival (ABC Survival): A Feasibility Study

Cancer is a leading cause of death worldwide. It is estimated that approximately 55,000 Canadians are surviving with brain tumors. It is projected that around 3000 persons will be diagnosed with brain and spinal cord tumors, and approximately 75 percent patients will not survive. Out of all brain cancers, high-grade gliomas \[Glioblastoma Multiforme (GBM)\] impose highest morbidity and mortality. Therefore, it is important to explore ways in which Investigators can improve and prolong the lives of patients suffering from brain cancers, particularly high-grade glioma, which is the most common and aggressive primary brain tumor. So far the Investigators know that the surgery, chemotherapy and radiotherapy are the three corner stones management options for these patients, and majority of the research have been conducted on these three major domains. Therefore, it is imperative to explore the other variables those may impact survival characteristics. One of the integral variables of the brain cancer surgery is anesthesia. Interestingly, the role of anesthetics was explored in some other non-brain solid organ tumor surgeries. It is observed that out of the two main types of anesthesia \[one is through intravenous (propofol) and other one is gaseous (sevoflurane)\], intravenous based anesthesia maintenance regime may delay the cancer progression and prolong the recurrence free period. In addition, two very large retrospective studies with approximately 11,000 and 18,000 patients respectively, showed that as compared to gaseous (volatile anesthetics) based, intravenous (propofol) based anesthesia conferred some protection against cancer progression and was also associated with lesser overall mortality. The exact nature of these protective mechanisms is not known but in animal and other laboratory-based experiments, propofol seems to inhibit cancer formation steps, delays inflammation and provide protection from cancer cell growth. This is a feasibility study for knowing various aspects of workflow; recruitment characteristics of participants and various obstacles in implying anesthesia based protocols so that the Investigators can conduct a well-designed multicenter international randomized study.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Health Network, TorontoUpdated: Jan 31, 2025Locations: 1
Eligibility criteria

Patient presenting between Jul 1, 2022 and Dec 28, 2023 for elective procedure [+2]

Patients of pediatric age group and pregnant patients [+6]

Status: Recruiting

Radical Surgery for Advanced Gastric- or GEJ-cancer With Oligometastatic Dissmination to the Liver

Offering treatment with potential to cure for participants with no such offer in today's standard treatment options, by offering metastatectomia and standard treatment with intention to cure i.e., neoadjuvant chemotherapy and gastrectomy for participants with gastric- og gastroeusofageal junction cancer. Including 20 participants from all 4 centres in Denmark able to perform the surgical procedures in question. Endpoints: 2-year overall survival.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Aarhus University HospitalUpdated: Oct 4, 2024Locations: 1
Eligibility criteria

Age > 18. [+5]

Patient with non-resectable cancer. [+7]

Status: Not yet recruiting

Comparison of Long-term Survival and Quality of Life After Minimally Invasive Esophagectomy Versus Open Esophagectomy

To analyze and compare the long-term recurrence-free survival rate, overall survival rate and quality of survival after minimally invasive esophagectomy and open esophagectomy, and to conduct subgroup analysis according to the type of esophageal cancer and pathological stage, etc., and to explore more deeply the differences between minimally invasive esophagectomy and open esophagectomy in terms of the benefits for different types of patients, so as to provide reference for the selection of the clinical surgical methods. We will also use the available data to analyze the influence of other factors on patients\&#39; long-term survival after surgery.

Participants needed: 1,474
Trial details
Biological sex: AllType: ObservationalSponsor: Qilu Hospital of Shandong UniversityUpdated: Nov 27, 2023Locations: 1
Eligibility criteria

Patients who had undergone esophageal cancer resection at the Department of Thor... [+1]

Status: Not yet recruiting

Incremental PD With Single Icodextrin Exchange

Objectives: To investigate the efficacy and safety of single daily icodextrin exchange for initiation of incremental peritoneal dialysis (PD). Subjects: Seventy-two incident PD patients. Methods: A single-center randomized controlled trial. Primary outcome: Change in residual kidney function in 48 weeks after recruitment.

Participants needed: 72
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: RenJi HospitalUpdated: Nov 8, 2023
Eligibility criteria

male or female patients aged 18 to 75 years; [+3]

documented anaphylaxis with icodextrin or glucose-based dialysate; [+6]

Status: Not yet recruiting

D2 Versus D3 Dissection in Laparoscopic Right Hemicolectomy

Evaluating the differences between D2 and D3 lymphadenectomy in laparoscopic right hemicolectomy in patients with right cancer colon post-operative outcome, intra-operative blood transfusion, post-operative ICU admission, anastomotic leakage, lymph node harvesting in the final specimen, and six months follow up and overall survival time after 5-years

Participants needed: 80
Trial details
Biological sex: AllType: InterventionalSponsor: General Committee of Teaching Hospitals and Institutes, EgyptUpdated: Sep 22, 2023Locations: 1
Eligibility criteria

Patients with right-side colon cancer (caecum, ascending, or hepatic flexure) [+3]

Emergency surgery (obstruction, perforation with generalized peritonitis), [+4]

Status: Recruiting

Neo-adjuvant Immunochemotheray Versus Neo-adjuvant Chemotherapy for Resectable Esophageal Carcinoma

The effect of neo-adjuvant immunochemotherapy on survival of patients with thoracic esophageal squamous cell carcinomas remains unknown. One of our objectives is to evaluate whether the neo-adjuvant immunochemotherapy Toripalimab (JS001) with cisplatin and paclitaxel followed by right thoracic approach esophagectomy with total 2-field lymph node dissection improves the overall survival of thoracic esophageal cancer patients versus neo-adjuvant chemotherapy.

Participants needed: 400
Trial details
Phase: Phase 3Age: 18-75Biological sex: AllType: InterventionalSponsor: Henan Cancer HospitalUpdated: Oct 4, 2022Locations: 1
Eligibility criteria

Histologic diagnosis of local advance squamous cell thoracic esophageal carcinom... [+10]

1. Multiple primary cancer. 2.Patients with infections disease that require trea...

Status: Not yet recruiting

Classified Treatment Strategy for De-novo Metastatic Breast Cancer After Systemic Adjuvant Therapy

For patients with de novo stage IV breast cancer, the current debate is whether local surgery can improve the survival of patients. There is no clinical study on the classification after systemic treatment of de novo stage IV breast cancer patients. In fact, the clinical stage of tumor can change with the change of treatment. For example, the stage Ⅲ of locally advanced breast cancer can down-staging to the stage Ⅱ after systemic treatment. Similarly, patients with stage Ⅳ can down-staging to stage Ⅱ or stage Ⅲ after systemic treatment. At this time, the patient can receive surgical treatment. Therefore, this study is to first treat de novo stage IV breast cancer patients with systemic treatment, according to the response after systemic treatment to give different treatment measures(surgery or continued systemic treatment). The investigators hope that this study will provide new ideas for the treatment of de novo stage IV breast cancer and other de novo stage IV cancers.

Participants needed: 362
Trial details
Age: 18-75Biological sex: FemaleType: InterventionalSponsor: Changhai HospitalUpdated: Jul 19, 2022
Eligibility criteria

Operable stage IV breast cancer patients,whose primary lesion is invasive breast... [+4]

Accompanied with other primary malignant tumors. [+3]

Status: Not yet recruiting

Comparative Study of Mitomycin and Lobaplatin in Advanced Colorectal Cancer Patients With Radical Surgery Combined With Hyperthermic Intraperitoneal Chemotherapy

This study is a prospective, randomized, comparative clinical trial conducted by Wuhan Union Hospital and aim to compare the therapeutic effects of Mitomycin and Lobaplatin in the treatment of advanced colorectal cancer patients with radical surgery combined with hyperthermic intraperitoneal chemotherapy

Participants needed: 201
Trial details
Phase: Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: Union Hospital, Tongji Medical College, Huazhong University of Science and TechnologyUpdated: Feb 21, 2022
Eligibility criteria

No chemoradiotherapy or other anti-tumor therapy before clinical trial performed... [+6]

A history of other malignant tumors within 5 years; [+6]

Status: Recruiting

Phase III Study of Concurrent Radiotherapy in Elderly Patients With Esophageal Squamous Cell Carcinoma (ESO-Shanghai 15)

So far, there is no specific clinical guideline for elderly patients (\>75 yr) with esophageal squamous cell carcinoma (ESCC). Patients with locally advanced ESCC were enrolled and randomly assigned to either definitive radiotherapy group (61.2Gy/34Fx) or the chemoradiotherapy group (50.4Gy/28Fx;Paclitaxel plus carboplatin). The primary end point was 3-year overall survival (OS). The second end points included life quality, radiation side effects and 3-yr cancer specific survival.

Participants needed: 320
Trial details
Age: 76+Biological sex: AllType: InterventionalSponsor: Fudan UniversityUpdated: Nov 2, 2021Locations: 3
Eligibility criteria

Indicates no limit on eligibility based on the sex of participants [+9]

Total radiotherapy dose cannot reach 61.2Gy/34Fx [+9]

Status: Recruiting

Long-term Survivorship of Discharged Patients With Malignant Tumor Based on Single-institutional Cancer Registry

Real-world studies on long-term prognosis in patients who underwent anti-tumor treatments during hospitalization from a hospital-based cancer registry in china.

Participants needed: 500,000
Trial details
Biological sex: AllType: ObservationalSponsor: Fudan UniversityUpdated: Aug 9, 2021Locations: 1
Eligibility criteria

All patients who completed tumor treatment (including surgery, radiotherapy, che...

Patients who have not been treated during hospitalization; [+1]

Status: Not yet recruiting

An Open-label, Multicentre, Phase II/III RCT of PFLL Versus GP Combined With JS001 as the First-line Therapy for mNPC

The treatment of distant metastasis is a key challenge for nasopharyngeal carcinoma because of poor outcomes, among which, chemotherapy is the cornerstone. However, many studies reported the use of different chemotherapy regimens to prolong the survival of metastatic nasopharyngeal carcinoma, while few of them focused on how to reduce the side effects of chemotherapy or improve the life quality of patients. Blocking the immune checkpoint is one of the effective strategies of tumor immunotherapy. Thus, we sought to find a proper chemotherapy regimen combined with PD-1 antibody JS001.

Participants needed: 622
Trial details
Phase: Phase 2, Phase 3Age: 18-60Biological sex: AllType: InterventionalSponsor: Sun Yat-sen UniversityUpdated: May 18, 2021Locations: 1
Eligibility criteria

Nasopharyngeal carcinoma diagnosed by pathology or cytology. [+13]

Allergic to monoclonal antibodies, any JS001 components, gemcitabine, cisplatin,... [+13]

Status: Recruiting

Salvage Hypofractionated Accelerated Versus Standard Radiotherapy for Biochemical Failure After Prostatectomy

Patients with a biochemical recurrence after radical prostatectomy for moderate- or high- risk prostate cancer are randomly assigned to hypofractionated, accelerated high dose radiation therapy group (65 Gy, 26 fractions) and a control group of standard treatment group (66 Gy, 33 fractions). The criteria for stratification at randomization include 1) risk groups, 2) androgen deprivation therapy, and 3) PSA before salvage radiation therapy, which affect biochemical recurrence. It is expected that hypofractionated, accelerated high dose radiation therapy will have a superiority in terms of biochemical control to conventional radiation therapy, and the present study would like to confirm this. In addition, we aimed to evaluate and compare the toxicity and quality of life index of two radiation therapy regimens.

Participants needed: 288
Trial details
Age: 20+Biological sex: MaleType: InterventionalSponsor: Asan Medical CenterUpdated: Jan 20, 2021Locations: 2
Eligibility criteria

Pathologically confirmed intermediate- or high-risk prostate cancer [+5]

Clinically gross recurrent tumor [+6]