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NCT05838300 · ClinicalTrials.gov registry record · NA

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

A NA study of Bariatric Surgery, sponsored by The University of Texas Health Science Center, Houston.

Recruiting
Registry status
NA
Development phase
54
Enrollment target
1
Study location

NCT05838300: Recruiting NA study of Bariatric Surgery, sponsored by The University of Texas Health Science Center, Houston.

NCT05838300 is a NA study of Bariatric Surgery that is actively recruiting participants, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 54 participants, below the 95-participant average among 15 other Bariatric Surgery trials with a reported enrollment target (43% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05838300, a NA study of Bariatric Surgery, is actively recruiting participants, sponsored by The University of Texas Health Science Center, Houston.

RECRUITING
Registry status
NA
Development phase
54 participants
Enrollment target
1
Study location

Study Summary

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.

Primary Outcome

This will be measured as a binary outcome variable (pain will be determined as VAS \>/= 4, and no pain will be VAS \< 4). This will be determined on post-operative day 1 as an average of the two pain scores.

Conditions Studied

Interventions

  • DEVICE Warm humidified CO2
  • DEVICE Dry CO2

Study Locations (1)

Texas

  • The University of Texas Health Science Center at Houston - Houston

Trial Details

FieldValue
Enrollment Target 54 participants
Start Date 2023-05-19
Est. Completion 2025-12-30
Phase NA

What NCT05838300 shows while recruiting

NCT05838300 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 54 participants, a relatively small participant target, below the 95-participant average among 15 other Bariatric Surgery trials with a reported enrollment target (43% lower).

The record links to 1 condition, with Bariatric Surgery appearing as the primary indexed condition, and to 2 interventions - of which Warm humidified CO2 is the first listed.

NCT05838300 reports a single indexed study location in Texas.

Frequently Asked Questions

What is clinical trial NCT05838300 about?

NCT05838300 is a clinical study titled "Lexion AP 50/30 Warmed Humidified Real Time CO2 Insufflation vs Airseal Recirculated CO2/Air Insufflation in Minimally Invasive Bariatric (Gastric Bypass) Surgery". 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.

What is the current status of trial NCT05838300?

This trial is currently recruiting. It is a NA study. The enrollment target is 54 participants. The study started on 2023-05-19. Estimated completion is 2025-12-30.

What conditions does trial NCT05838300 study?

This clinical trial studies the following conditions: Bariatric Surgery.

What interventions are being tested in trial NCT05838300?

The interventions under investigation include: Warm humidified CO2 (DEVICE), Dry CO2 (DEVICE).

Who is sponsoring clinical trial NCT05838300?

This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05838300 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Bariatric Surgery

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05838300's enrollment target sits among peer trials

54 6th of 15 higher than 10 of 15 other Bariatric Surgery trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Bariatric Surgery trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05838300, the US trial registry maintained by the National Library of Medicine. NCT05838300 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.