Actively Recruiting
ESPBs vs TAPs for Satisfactory Analgesia Following DIEP Surgery
Led by University of Kansas Medical Center · Updated on 2025-07-09
102
Participants Needed
1
Research Sites
165 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Breast cancer is the second most common cancer diagnosed in American women . For patients who have undergone surgical mastectomy, autologous breast reconstruction is an alternative option to breast implants. Deep Inferior Epigastric Perforator (DIEP) flaps are the gold standard for autologous breast reconstruction . Effective pain control following surgery is imperative and ultrasound-guided bilateral transversus abdominis plane blocks (TAPs) with the infiltration of local anesthetics, such a bupivacaine are a common regional technique of choice . A newer described technique, bilateral Erector Spinae Plane blocks (ESPBs) (which also are an infiltration of local anesthetic) present as an alternative approach for post-operative analgesia. ESPBs have been proven efficacious in reducing intra- and post-operative opioid requirements, lessening the need for rescue analgesics in other similar surgical procedures. The hypothesis is that preoperative bilateral ESPBs could provide equivalent pain control as a regional analgesic for patients undergoing DIEP flap surgery when compared to preoperative bilateral TAPs
CONDITIONS
Official Title
ESPBs vs TAPs for Satisfactory Analgesia Following DIEP Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult women with breast cancer
- ASA physical status classification 1 to 3
- Scheduled for DIEP flap surgery
You will not qualify if you...
- Chronic opioid use
- Contraindications to local anesthetics or regional analgesia
- Inability to communicate pain intensity using a numeric scale
AI-Screening
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Trial Site Locations
Total: 1 location
1
University of Kansas Medical Center
Kansas City, Kansas, United States, 66160
Actively Recruiting
Research Team
R
Rachel Henning
CONTACT
M
Manuel Clark
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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