Clinical trial · Interventional
Rhomboid Intercostal and Subserratum Plane Block for Minimally Invasive Esophagectomy
Clinical Study of Rhomboid Intercostal and Subserratum Plane Block for Postoperative Analgesia in Minimally Invasive Esophagectomy
NCT06092944CI-TRIAL-00070682unknownN/AClinicalTrials.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 objective is to investigate the safety and effectiveness of rhomboid intercostal and subserratum plane (RISS) block for postoperative analgesia after minimally invasive McKeown esophagectomy (MIE-McKeown).
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 |
|---|---|---|---|
| Esophagus Cancer | Esophageal Neoplasm | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (4)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Catheterization | Procedure | — | UNRESOLVED |
| Continuous nerve block | Procedure | — | UNRESOLVED |
| PCIA | Procedure | — | UNRESOLVED |
| Single nerve block | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- continuous RISS group
- description
- Patients were given continuous RISS plane block in addition to patient controlled intravenous analgesia.
- interventionNames
- Procedure: Catheterization
- Procedure: Single nerve block
- Procedure: Continuous nerve block
- Procedure: PCIA
- type
- EXPERIMENTAL
- label
- single RISS group
- description
- Patients were given single RISS plane block in addition to patient controlled intravenous analgesia.
- interventionNames
- Procedure: Single nerve block
- Procedure: PCIA
- type
- ACTIVE_COMPARATOR
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: * Patients received MIE-McKeown surgery and were confirmed by postoperative pathology; Age 18-75 years old * body mass index (BMI) : 18.5\~23.9kg/m2; * American Society of Anesthesiologists (ASA) grade: Ⅰ\~Ⅱ; * Clear consciousness, no cognitive impairment; * Patients informed to participate in the study and signed informed consent. Exclusion Criteria: * Infection of the puncture site, abnormal platelet or coagulation function; * Patients with drug allergy involved in this study; * Long-term use of analgesic, sedative drugs or a history of heavy drinking; * Patients with chronic painful diseases; * With severe heart, liver, kidney and lung dysfunction; * Infectious diseases, blood, immune, circulatory system diseases; -Communication barriers, can not cooperate with the scale assessment; - * Other situations not suitable for this study.
References
Publications (0)
Data not yet available
No reference posted for this study.