Relationship of Nutritional Status to Chemotherapy Treatment Completion and Outcomes in Cancer Patients

NCT ID: NCT07059598

Last Updated: 2025-07-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

209 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-08-12

Study Completion Date

2025-03-01

Brief Summary

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This non-interventional, prospective, non-drug observational study is designed to observe the effect of the nutritional status of metastatic and non-metastatic gastric, colon and lung cancer patients on their cancer chemotherapy treatment completion rates.

Detailed Description

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Conditions

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Cancer-related Malnutrition

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Subject or subject's legally acceptable representative (LAR) has voluntarily signed and dated an ICF approved by an IEC, or any other applicable privacy authorization prior to any participation in the study.
* 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 known dementia, brain metastases, eating disorders, history of significant neurological or psychiatric disorder, any other psychological condition, serious illness or medical condition that may interfere with study completion.
* 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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Abbott Nutrition

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Çukurova Üniversitesi Balcalı Hastanesi Sağlık Uygulama ve Araştırma Hastanesi

Sarıçam, Adana, Turkey (Türkiye)

Site Status

Hacettepe Üniversitesi Tıp Fakültesi Onkoloji Hastanesi

Altındağ, Ankara, Turkey (Türkiye)

Site Status

Ankara Etlik Şehir Hastanesi

Yenimahalle, Ankara, Turkey (Türkiye)

Site Status

Sağlık Bilimleri Üniversitesi Dr. Abdurrahman Yurtaslan Ankara Onkoloji Eğitim Ve Araştırma Hastanesi

Yenimahalle, Ankara, Turkey (Türkiye)

Site Status

Bursa Uludağ Üniversitesi Tıp Fakültesi Hastanesi Sağlık Uygulama ve Araştırma Hastanesi

Ortahisar, Bursa, Turkey (Türkiye)

Site Status

Dicle Ünversitesi Hastaneleri Tıp Fakültesi Hastanesi

Sur, Diyarbakır, Turkey (Türkiye)

Site Status

S.B. İstanbul Medeniyet Üniversitesi Göztepe Eğitim Ve Araştırma Hastanesi

Kadıköy, Istanbul, Turkey (Türkiye)

Site Status

İstanbul Maslak Acıbadem Hastanesi

Sarıyer, Istanbul, Turkey (Türkiye)

Site Status

Amerikan Hastanesi

Şişli, Istanbul, Turkey (Türkiye)

Site Status

Ege Üniversitesi Hastanesi Sağlık Uygulama ve Araştırma Merkezi

Bornova, İzmir, Turkey (Türkiye)

Site Status

İnönü Üniversitesi Turgut Özal Tıp Merkezi

Battalgazi, Malatya, Turkey (Türkiye)

Site Status

Karadeniz Teknik Üniversitesi Farabi Hastanesi

Ortahisar, Trabzon, Turkey (Türkiye)

Site Status

Akdeniz Üniversitesi Sağlık Araştırma ve Uygulama Merkezi Hastanesi

Antalya, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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DA28

Identifier Type: -

Identifier Source: org_study_id

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