Relationship of Nutritional Status to Chemotherapy Treatment Completion and Outcomes in Cancer Patients
NCT ID: NCT07059598
Last Updated: 2025-07-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
209 participants
OBSERVATIONAL
2022-08-12
2025-03-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Malnutrition and Sarcopenia Screening in Chemotherapy Patients
NCT07163286
Nutritional Supplements in Improving Quality of Life During First-Line Chemotherapy in Patients With Metastatic Gynecological Cancer
NCT00905658
Nutritional Risk and Mucositis in Patients With Head and Neck Carcinoma Receiving Chemoradiation
NCT00577902
Nutritional Preferences and Product Accessibility in Oral Nutritional Supplements in Participants With Breast, Colorectal, Upper Gastrointestinal, or Prostate Cancer
NCT03563352
Nutritional Supplementation in Reducing Complications in Patients With Locally Advanced Esophageal Cancer Undergoing Chemotherapy, Radiation Therapy, and/or Surgery
NCT04029857
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Ambulatory and inpatient subject.
* Subject recently (within the last month) or newly diagnosed to have metastatic or non-metastatic gastric, colon and lung cancer.
* Subject is recently receiving chemotherapy or recently prescribed to begin chemotherapy treatment per standard of care (within the last month) or candidates who will receive chemotherapy.
* Subject has a life expectancy greater than 6 months.
Exclusion Criteria
* Subject has malignant tumors other than treated DCIS, fully treated non-melanoma skin cancer, curatively resected in-situ cervical cancer or other curative treated tumors (except stomach, colon and lung cancer) for \> 5 years.
* Subject has bone marrow metastasis.
* Subject is lactating.
* Subject is participating in another study that has not been approved as a concomitant study.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Abbott Nutrition
INDUSTRY
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Çukurova Üniversitesi Balcalı Hastanesi Sağlık Uygulama ve Araştırma Hastanesi
Sarıçam, Adana, Turkey (Türkiye)
Hacettepe Üniversitesi Tıp Fakültesi Onkoloji Hastanesi
Altındağ, Ankara, Turkey (Türkiye)
Ankara Etlik Şehir Hastanesi
Yenimahalle, Ankara, Turkey (Türkiye)
Sağlık Bilimleri Üniversitesi Dr. Abdurrahman Yurtaslan Ankara Onkoloji Eğitim Ve Araştırma Hastanesi
Yenimahalle, Ankara, Turkey (Türkiye)
Bursa Uludağ Üniversitesi Tıp Fakültesi Hastanesi Sağlık Uygulama ve Araştırma Hastanesi
Ortahisar, Bursa, Turkey (Türkiye)
Dicle Ünversitesi Hastaneleri Tıp Fakültesi Hastanesi
Sur, Diyarbakır, Turkey (Türkiye)
S.B. İstanbul Medeniyet Üniversitesi Göztepe Eğitim Ve Araştırma Hastanesi
Kadıköy, Istanbul, Turkey (Türkiye)
İstanbul Maslak Acıbadem Hastanesi
Sarıyer, Istanbul, Turkey (Türkiye)
Amerikan Hastanesi
Şişli, Istanbul, Turkey (Türkiye)
Ege Üniversitesi Hastanesi Sağlık Uygulama ve Araştırma Merkezi
Bornova, İzmir, Turkey (Türkiye)
İnönü Üniversitesi Turgut Özal Tıp Merkezi
Battalgazi, Malatya, Turkey (Türkiye)
Karadeniz Teknik Üniversitesi Farabi Hastanesi
Ortahisar, Trabzon, Turkey (Türkiye)
Akdeniz Üniversitesi Sağlık Araştırma ve Uygulama Merkezi Hastanesi
Antalya, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
DA28
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.