Clinical trial · Interventional
TPVB, PECSB, ESPB for Postmastectmy Pain
A Comparative Study Between Ultrasound-guided Thoracic Paravertebral Block, Pectoral Nerves Block, and Erector Spinae Block for Pain Management in Cancer Breast Surgeries. A Randomized Controlled Study
- 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)
Aim of the work The aim of the study is to compare between the effects of ultrasound guided thoracic paravertebral block, pectoral nerve block II, and erector spinae block in management of pain during cancer breast surgeries. The hypothesis of the study is that the three groups will give comparative results.
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 |
|---|---|---|---|
| Pain, Postoperative | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| IV morphine | Drug | — | UNRESOLVED |
| Ultrasound guided block | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (4)
- type
- PLACEBO_COMPARATOR
- label
- Control Group (D)
- description
- Patient will receive opioid only for management of their perioperative pain
- interventionNames
- Drug: IV morphine
- type
- ACTIVE_COMPARATOR
- label
- Paravertebral block Group (A)
- description
- Will receive thoracic paravertebral block
- interventionNames
- Procedure: Ultrasound guided block
- Drug: IV morphine
- type
- ACTIVE_COMPARATOR
- label
- Pectoral block Group (B)
- description
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
- Maximum age
- 60 Years
Show eligibility criteria text
Inclusion Criteria: 1. ASA physical status classification class I or II 2. Age group 18 - 60 years of the female gender 3. Patients undergoing breast cancer surgeries Exclusion Criteria: 1. Patient refusal 2. History of hypersensitivity to local anesthetics 3. Bleeding disorders or patients receiving anticoagulants 4. Spine or chest wall deformities 5. Pregnancy 6. Local infection at the site of injection.
References
Publications (0)
Data not yet available