Clinical trial · Interventional
Comparison Immune Response in Paravertebral and Erector Spinal Plane Block in Breast Cancer Patients
Immunologic Response in Breast Cancer Before and After Application of Paravertebral and Erector Spinae Plane Block
- 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 goal of this clinical trial is to find the difference in immune response between two types of regional anesthesia in female patients suffering from breast cancer. The main question it aims to answer is there a difference in the immune response between paravertebral block and erector spinal plane block. Hypothresis of the study is that paravertebral block with propofol induces less immune response in surgical treatment of breast cancer patients than erector spinal plane block. Participants will be asked to sign the informant consent. They will be given either paravertebral block or erector spinae plane block with general anesthesia using propofol. Their venous blood will be taken 1 hour prior surgery and 24 and 48 hours after surgery.
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 |
|---|---|---|---|
| Breast Cancer - Female | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Blood draw for the laboratory assessment | Procedure | — | UNRESOLVED |
| Regional Anesthetic Injection | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- Draw of venous blood 1 hour prior surgery
- description
- Draw of venous blood and application of paravertebral or erector spinae plane block
- interventionNames
- Procedure: Regional Anesthetic Injection
- type
- EXPERIMENTAL
- label
- Draw of venous blood 24 hours after surgery
- description
- Draw of venous blood
- interventionNames
- Procedure: Blood draw for the laboratory assessment
- type
- EXPERIMENTAL
- label
- Draw of venous blood 48 hours after surgery
- description
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: * ASA I and ASA II status, normal BMI Exclusion Criteria: * ASA III and ASA IV status, coagulopathy, chronic opioid use, diabetes, local infection of the skin
References
Publications (0)
Data not yet available