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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 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.

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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.

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 the Registry Record Tells You About NCT05838300

The ClinicalTrials.gov registry entry for NCT05838300 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 54 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 95-participant average among 15 other Bariatric Surgery trials with a reported enrollment target (43% lower). The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.

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 1 study location spanning 1 distinct geographic area - top geographies include 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.

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