Clinical trial · Observational
Quality of Life Among Long-Term Survivors of Resected Gastric Cancer
NCT00598546CI-TRIAL-00002453completedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose of this study is to find out how you feel about the quality of your life after having had surgery to remove your stomach tumor. Some patients continue to experience different problems after stomach surgery, even when the surgery was more than three years ago. The purpose of this study is to find out the specific things that may continue to affect patients' quality of life after a major operation.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Gastric Cancer | Malignant Gastric Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| EORTC QLQ-C30, QLQ-STO22, and MSK-10 | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- 1
- interventionNames
- Behavioral: EORTC QLQ-C30, QLQ-STO22, and MSK-10
Primary outcomes (1)
- measure
- Instrument: EORTC QLQ-C30, QLQ-STO22, and MSK-10. The intent of this study is to assess QOL in long-term survivors of all surgical procedures performed for the treatment of gastric cancer.
- timeFrame
- 5 years
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Male and female patients * Age 18 or older * Diagnosis of adenocarcinoma of the stomach * Patient had curative surgical resection, including proximal, distal, or total gastrectomy * Patient is at least three years NED * Provide informed consent * Fluent in English Exclusion Criteria: * Psychiatric or psychological abnormality precluding informed consent or ability to complete questionnaires * Non-psychiatric disorder causing a lack of capacity to give consent or an inability to complete questionnaires (ie dementia, stroke)
References
Publications (0)
Data not yet available
No reference posted for this study.