Clinical trial · Observational
Prolonged Extubation in Gastric Cancer With OSA
An Exploratory Study on the Impact of Prolonged Postoperative Endotracheal Extubation Time on Postoperative Complications in Gastric Cancer Patients With Severe Obstructive Sleep Apnea
NCT07362706CI-TRIAL-00101499Gastric Cancerenrolling by invitationClinicalTrials.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 study aims to investigate the effect of prolonged tracheal intubation removal on the incidenceof postoperative complications in patients with gastric cancer complicated with severe obstructive sleepapnea.
Conditions
Conditions (2)
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 (GC) | Malignant Gastric Neoplasm | CURATED_BROADER | 0.80 |
| Obstructive Sleep Apnea | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Prolonging the duration of postoperative endotracheal intubation before extubation. | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- Postoperative complications
- timeFrame
- 48-72 hour
- description
- The incidence of postoperative complications in patients with gastric cancer complicated with severe obstructive sleepapnea.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 85 Years
Show eligibility criteria text
Inclusion Criteria: 1. Patients preoperatively diagnosed with resectable gastric cancer 2. Patients without distant organ metastasis 3. Patients with preoperative Overnight Cardiorespiratory Sleep Testing (OCST) or Polysomnography (PSG) results showing Apnea-Hypopnea Index (AHI) \>30 events/hour and SaO₂ \<80% 4. Patients with cardiopulmonary function deemed suitable for surgery 5. Patients aged 18-85 years 6. Patients who voluntarily joined this study and provided written informed consent Exclusion Criteria: 1. Patients with a history of or concurrent other malignant tumors 2. Patients who underwent palliative resection 3. Subjects who experienced acute cardiovascular or cerebrovascular events (e.g., acute cerebral infarction, acute coronary syndrome) within the past 3 months, or whose cardiovascular clinical symptoms/diseases are not well-controlled 4. Patients with a history of psychotropic drug abuse that cannot be abstained, or those with psychiatric disorders 5. Patients with concomitant diseases that, in the investigator's judgment, seriously endanger the patient's safety or affect the completion of the study
References
Publications (0)
Data not yet available
No reference posted for this study.