RECRUITING

Lexion AP 50/30 Warmed Humidified Real Time CO2 Insufflation Vs Airseal Recirculated CO2/Air Insufflation in Minimally Invasive Bariatric (Gastric Bypass) Surgery

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

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: a Randomized Controlled Study of Clinical Evaluation

Quick Facts

Study Start:2023-05-19
Study Completion:2025-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05838300

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 65 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * elective bariatric primary or revision procedures and hiatal hernia repair procedures for all indications.
  1. * emergency surgery, reoperation within 30 days
  2. * patients who are taking pain medications (narcotics) daily preoperatively for whatever reason
  3. * history of narcotics addiction
  4. * paraplegic and quadriplegic patients
  5. * dementia or altered mental status
  6. * patients on steroids
  7. * pregnant women
  8. * psychiatric patients
  9. * minors
  10. * unable to give informed consent

Contacts and Locations

Study Contact

Erik B Wilson, MD,FACS
CONTACT
713-500-7277
Erik.B.Wilson@uth.tmc.edu
Angielyn Rivera
CONTACT
713-416-1350
Angielyn.R.Rivera@uth.tmc.edu

Principal Investigator

Erik Wilson, MD, FACS
PRINCIPAL_INVESTIGATOR
The University of Texas Health Science Center, Houston

Study Locations (Sites)

The University of Texas Health Science Center at Houston
Houston, Texas, 77030
United States

Collaborators and Investigators

Sponsor: The University of Texas Health Science Center, Houston

  • Erik Wilson, MD, FACS, PRINCIPAL_INVESTIGATOR, The University of Texas Health Science Center, Houston

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-05-19
Study Completion Date2025-06-30

Study Record Updates

Study Start Date2023-05-19
Study Completion Date2025-06-30

Terms related to this study

Keywords Provided by Researchers

  • carbon dioxide
  • minimally invasive surgery

Additional Relevant MeSH Terms

  • Bariatric Surgery