Impact of Pectoral Versus Paravertebral Blocks on Pain and Physical Well-Being in Implant-Based Breast Reconstruction

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAmy Colwell

About this trial

The broad aim of this study is to compare the effectiveness of paravertebral and pectoral blocks on pain and physical well-being of patients undergoing immediate implant-based breast reconstruction.

Eligibility criteria

Qualifiers

Adult patient 18 years or older

Scheduled for unilateral or bilateral immediate implant-based breast reconstruction

Therapeutic or prophylactic indication

Patient understands the study procedures and objectives and is willing to participate

Disqualifiers

Delayed breast reconstruction

Allergy or contraindication to local anesthetics (PVB or PECS blocks)

History of radiation therapy

Planned sedation or general anesthesia protocol variation

Trial design

Treatments tested in this trial

  • Paravertebral block (single injection)
  • Pectoral block

Treatment groups

212 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Amy Colwell

Lead sponsor

Massachusetts General Hospital

Sponsor institution