Abdominal Wall Block Study
Completed · Not applicable
Conditions studied: Umbilical Hernia, Obesity
In brief
Compare the ability of the transversus abdominis plane block (TAPB) and rectus sheath block (RSB) to provide surgical anesthesia for overweight and obese patients undergoing umbilical hernia surgery.
Key facts
- Study ID
- NCT03074240
- Run by
- University of Florida
- People needed
- 15
- Starts
- 2017-08-07
- Expected to finish
- 2021-07-12
- Last updated by the study team
- 2024-05-30
Who can join
Age: 18 and older, up to 99. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients ≥ 18 years of age undergoing umbilical hernia repair
- Overweight and obese individuals (defined as a body mass index of ≥ 25 and 30 kg/m2, respectively)
- Ability to understand and provide informed consent
You may not qualify if…
- Patient refusal or inability to provide informed consent
- True allergy, not sensitivity, local anesthetics
- True allergy, not sensitivity, Propofol
- True allergy, not sensitivity, general anesthetic agents
- Pregnancy
- Severe hepatic impairment
- Evidence of infection at or near the proposed needle insertion site
- Any sensorimotor deficit, whether acute or chronic, as determined by the PI
- Chronic use of opioid medication
Where it is running
- Malcom Randall VA Medical Center — Gainesville, Florida, United States
Full record on ClinicalTrials.gov
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