Actively Recruiting
Lexion AP 50/30 Warmed Humidified Real Time CO2 Insufflation vs Airseal Recirculated CO2/Air Insufflation in Minimally Invasive Bariatric (Gastric Bypass) Surgery
Led by The University of Texas Health Science Center, Houston · Updated on 2025-06-13
54
Participants Needed
1
Research Sites
136 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to To determine the effect of warm and humidified (WH) carbon dioxide (CO2) on post-operative pain/analgesia requirement in patients undergoing laparoscopic bariatric surgery.
CONDITIONS
Official Title
Lexion AP 50/30 Warmed Humidified Real Time CO2 Insufflation vs Airseal Recirculated CO2/Air Insufflation in Minimally Invasive Bariatric (Gastric Bypass) Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Elective bariatric primary or revision procedures and hiatal hernia repair for any reason
You will not qualify if you...
- Emergency surgery or reoperation within 30 days
- Daily use of narcotic pain medications before surgery
- History of narcotic addiction
- Paraplegic or quadriplegic patients
- Dementia or altered mental status
- Use of steroids
- Pregnant women
- Psychiatric patients
- Minors
- Unable to give informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The University of Texas Health Science Center at Houston
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
E
Erik B Wilson, MD,FACS
CONTACT
A
Angielyn Rivera
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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