Clinical trial · Observational
Early Recovery After Surgery Protocol in Improving Quality of Life in Participants With Stage 0-IIIC Gastric Cancer Undergoing Surgery
Gastric Cancer Enhanced Recovery After Surgery Pathway
NCT03997162CI-TRIAL-00103926active not recruitingClinicalTrials.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)
This phase II trial studies how well an early recovery after surgery protocol works in enhancing quality of life in participants with stage 0-IIIC gastric cancer undergoing surgery. The early recovery after surgery protocol may decrease pain and nausea, promote bowl function, decrease the number of days hospitalized, and improve a participant's ability to function normally after surgery.
Conditions
Conditions (18)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Clinical Stage 0 Gastric Cancer AJCC v8 | — | UNRESOLVED | — |
| Clinical Stage I Gastric Cancer AJCC v8 | — | UNRESOLVED | — |
| Clinical Stage IIA Gastric Cancer AJCC v8 | — | UNRESOLVED | — |
| Clinical Stage IIB Gastric Cancer AJCC v8 | — | UNRESOLVED | — |
| Clinical Stage II Gastric Cancer AJCC v8 | — | UNRESOLVED | — |
| Clinical Stage III Gastric Cancer AJCC v8 | — | UNRESOLVED | — |
| Gastric Adenocarcinoma | Gastric Adenocarcinoma | ONTOLOGY_EXACT | 0.98 |
| Pathologic Stage 0 Gastric Cancer AJCC v8 | — | UNRESOLVED | — |
| Pathologic Stage IA Gastric Cancer AJCC v8 | — | UNRESOLVED | — |
| Pathologic Stage IB Gastric Cancer AJCC v8 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Best Practice | Other | — | UNRESOLVED |
| Quality-of-Life Assessment | Other | — | UNRESOLVED |
| Questionnaire Administration | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- Observational (ERAS protocol)
- description
- Participants complete standard of care early recovery after surgery protocol beginning the day before surgery to day 6 after surgery.
- interventionNames
- Other: Best Practice
- Other: Quality-of-Life Assessment
- Other: Questionnaire Administration
Primary outcomes (2)
- measure
- Length of stay
- timeFrame
- from date of surgery to discharge from hospital, assessed up to 30 days
- description
- Will determine the length of hospital stay after surgery
- measure
- Rate and type of post-operative complications
- timeFrame
- Up to 1 year
Secondary outcomes (2)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 99 Years
Show eligibility criteria text
Inclusion Criteria: * Patients to be included are those with a biopsy proven diagnosis of gastric adenocarcinoma who are undergoing curative gastric surgery or prophylactic total gastrectomy for genetic risk. * Patients with clinical stage 0-IIIC will be included. * Any performance status and any life expectancy. * The effects of gastric surgery on the developing fetus are unknown. For this reason, women of childbearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control or abstinence) prior to study entry and for six months following duration of study participation. Should a woman become pregnant or suspect that she is pregnant while participating on the trial, she should inform her treating physician immediately. * All subjects must have the ability to understand and the willingness to sign a written informed consent. * Prior therapy will not be used as a limitation in this study. Exclusion Criteria: * Patients will be excluded if they are not candidates for surgery * Patients will be excluded from the study if they have had prior gastric surgery, with the exception of a gastrostomy tube. * Subjects, who in the opinion of the investigator, may not be able to comply with the safety monitoring requirements of the study.
References
Publications (0)
Data not yet available
No reference posted for this study.