Trials / Recruiting
RecruitingNCT04513808
Total Intravenous Anesthesia and Recurrence Free Survival
Total IntraVenous AnesthesIa and ReCurrence-free Survival AfTer EsOphageal CanceR SurgerY
- Status
- Recruiting
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 1,614 (estimated)
- Sponsor
- The Cleveland Clinic · Academic / Other
- Sex
- All
- Age
- 18 Years – 90 Years
- Healthy volunteers
- Not accepted
Summary
The investigators propose to compare recurrence-free survival in patients having potentially curative (Stages 1-3) surgery for esophageal cancer who will be randomly assigned to propofol-based total intravenous anesthesia or sevoflurane-based balanced general anesthesia.
Detailed description
The investigators will test the primary hypothesis that recurrence-free survival after esophageal cancer surgery is longer in patients randomized to propofol-based total intravenous anesthesia than to volatile sevoflurane anesthesia. The investigators will test the secondary hypotheses that propofol-based total intravenous anesthesia: 1) speeds discharge from the ICU; 2) speeds discharge from the hospital; and, 3) improves the quality of recovery, as assessed by QoR-15 on postoperative day 2.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Propofol-based total intravenous anesthesia | Propofol-based total intravenous anesthesia, titrated to clinical need. |
| DRUG | Sevoflurane intravenous anesthesia | Sevoflurane intravenous anesthesia, titrated to clinical need. |
Timeline
- Start date
- 2020-08-15
- Primary completion
- 2025-12-01
- Completion
- 2027-12-01
- First posted
- 2020-08-14
- Last updated
- 2024-12-04
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT04513808. Inclusion in this directory is not an endorsement.