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Low Gas Pressure vs Standard Gas Pressure in Weight-Loss Surgery

13 luglio 2026 aggiornato da: Weill Medical College of Cornell University

Comparison Between Low Pressure (8 mmHg) AirSeal Insufflation vs Standard Pressure (15 mmHg) Pneumoperitoneum on Postoperative Recovery in Bariatric Surgery: A Randomized Controlled Trial

During weight-loss surgery that is done using a robot, the surgeon needs to put carbon dioxide gas into the belly to lift the belly wall. This is done so the surgeon can adequately see all the body organs and operate safely. Many surgeons currently use a standard pressure of 15 mmHg (a unit to measure pressure). However, many patients find the use of this pressure to be painful after surgery. New research has shown that using a lower pressure with a device called "AirSeal" can safely reduce pain and lead to faster recovery after surgery.

The goal of this clinical trial is to learn if using a lower gas pressure with the AirSeal device during weight-loss surgery, compared to standard gas pressure with conventional devices, helps adults feel less pain and recover faster.

The study includes adults aged 18 or older having robotic weight-loss surgery (sleeve gastrectomy or Roux-en-Y gastric bypass) at New York-Presbyterian Hospital/Weill Cornell Medical Center.

The main questions this clinical trial aims to answer are:

  1. Does using lower gas pressure shorten the time people spend in the recovery room after surgery?
  2. Does using lower gas pressure lead to less pain and reduce the need for pain medicine after surgery?

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Descrizione dettagliata

Minimally invasive bariatric surgeries require the use of pneumoperitoneum, which is a standard of care as it creates a working environment to utilize minimally invasive tools to accomplish surgical procedures. However, there is no uniform standard pressure (usually between 12-15 mmHg). Moreover, maintaining the same pressure throughout the procedure can be inconsistent at best. Elevations in pneumoperitoneum cause significant stretch to the peritoneum which results in significant postoperative pain, longer post-anesthesia care unit (PACU) stay times, and higher opioid consumption. These effects are amplified to a higher degree in patients with severe obesity. If the pressures can be maintained and set to lower levels, then patients may have the opportunity to recover in the immediate postoperative period.

The AirSeal Robotic Solution (CONMED Corporation) is an FDA 510(k)-cleared carbon dioxide insufflation device that is indicated for use in robotic-assisted surgery.

This study is a prospective, single-center, single-blind, double-arm parallel-group randomized controlled trial that aims to determine if the use of low-pressure (8 mmHg) AirSeal insufflation, compared to standard-pressure (15 mmHg) pneumoperitoneum, provides superior patient outcomes in terms of post-operative recovery time and convalescence.

During the preoperative evaluation, participants will be consented and enrolled into the trial. Participants will then be randomly allocated to either low-pressure AirSeal insufflation (8 mmHg) or standard-pressure pneumoperitoneum (15 mmHg). Patients and outcome assessors will be blinded to allocation; however, for safety purposes, the operating surgeon and anesthesiologist cannot be blinded.

Intraoperative data (including operation time, estimated blood loss, abdominal pressure, and pressure deviations) will be recorded. Participant data related to comorbidities (i.e. body mass index, American Society of Anesthesiologists physical status, hypertension, diabetes, obstructive sleep apnea, chronic obstructive pulmonary disease/asthma, and smoking status) will be collected from the electronic medical record.

Tipo di studio

Interventistico

Iscrizione (Stimato)

100

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

  • Stati Uniti
    • New York
      • New York, New York, Stati Uniti, 10021
        • New York-Presbyterian/Weill Cornell Medical Center GI Metabolic and Bariatric Surgery
        • Investigatore principale:
          • Cheguevara Afaneh, MD
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  • Aged 18 years or older
  • Scheduled to undergo robotic-assisted Roux-en-Y gastric bypass or sleeve gastrectomy at New York-Presbyterian/Weill Cornell Medical Center
  • Obesity (body mass index≥40kg/m2 or ≥35kg/m2 with serious obesity-related health conditions)
  • American Society of Anesthesiologists physical status I-III
  • Able to understand and provide written informed consent in English

Exclusion Criteria:

  • American Society of Anesthesiologists physical status IV or higher (i.e. a severe systemic disease that is a constant threat to life such as decompensated heart failure)
  • Chronic opioid use (≥30 morphine milligram equivalents per day for ≥30 days within the past 6 months)
  • Current pregnancy
  • Inability to understand and provide informed consent in English
  • Inability to provide informed consent due to cognitive impairment or other conditions impacting decision-making capacity
  • Scheduled open or laparoscopic Roux-en-Y gastric bypass or sleeve gastrectomy

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Altro
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Doppio

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Low-pressure pneumoperitoneum (AirSeal)

Participants who are assigned to this arm will receive 8 mmHg pneumoperitoneum using the AirSeal Robotic Solution device.

The AirSeal Robotic Solution device is a FDA 510(k)-cleared carbon dioxide insufflation platform with valveless trocar technology that helps to maintain stable intra-abdominal pressure during surgery.
Dispositivo: AirSeal Robotic Solution

The experimental intervention is low-pressure pneumoperitoneum at 8 mmHg using the AirSeal Robotic Solution device.

The AirSeal Robotic Solution (CONMED Corporation) is an FDA 510(k)-cleared carbon dioxide insufflation device that is indicated for use in robotic-assisted surgery. It consists of a console, tri-lumen filtered tube set, and access ports that function as valveless trocars.

The console of the device is mounted on a cart and regulates carbon dioxide flow and smoke evacuation by continuously measuring the intra-abdominal pressure. The trilumen filtered tube set carries carbon dioxide to the abdomen, transmits pressure information back to the console, and returns gas from the abdomen for smoke evacuation and filtration. These features allow for the device to operate in the "AirSeal" mode, whereby the pressure within the abdomen is effectively kept constant. The valveless trocars are access ports for the minimally invasive tools to enter the abdominal cavity.
Comparatore attivo: Standard-pressure pneumoperitoneum
Participants who are assigned to this arm will receive 15 mmHg pneumoperitoneum using the conventional insufflation machine at New York-Presbyterian/Weill Cornell Medical Center.
Altro: Standard-pressure pneumoperitoneum (15 mmHg)
The control intervention is standard-pressure pneumoperitoneum set at a pressure of 15 mmHg. This will be delivered using the operating room's conventional valved-trocar carbon dioxide insufflator.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Average post-anesthesia care unit (PACU) length of stay in minutes from PACU admission to PACU discharge order
Lasso di tempo: From PACU arrival (5 minutes post-surgery) to PACU discharge-order (1 to 4 hours post-surgery)

The PACU is the area where participants recover from anesthesia after surgery. The PACU recovery time will be computed in minutes as the interval between the documented PACU arrival timestamp and the documented PACU discharge-order timestamp which will both be abstracted from the institutional electronic medical record.

The discharge-order timestamp represents the clinical decision that the participant is fit to leave the PACU and is therefore not confounded by factors such as transport delays.
From PACU arrival (5 minutes post-surgery) to PACU discharge-order (1 to 4 hours post-surgery)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Average numeric rating scale (NRS) pain score (0-10) at PACU admission
Lasso di tempo: PACU arrival (5 minutes post-surgery)

Postoperative pain intensity is measured using a verbally administered numeric rating scale (NRS) ranging from 0 to 10.

0 indicates no pain while 10 indicates the worst pain that the participant can imagine or has experienced. The score will be recorded as an integer.

The pain scores will be taken from the participants within 5 minutes of documented PACU arrival.
PACU arrival (5 minutes post-surgery)
Average numeric rating scale (NRS) pain score (0-10) at PACU discharge
Lasso di tempo: PACU discharge (1-4 hours post-surgery)

Postoperative pain intensity is measured using a verbally administered numeric rating scale (NRS) ranging from 0 to 10.

0 indicates no pain while 10 indicates the worst pain that the participant can imagine or has experienced. The score will be recorded as an integer.

The pain scores will be taken from the participants within 10 minutes of PACU discharge order time stamp.
PACU discharge (1-4 hours post-surgery)
Average numeric rating scale (NRS) pain score (0-10) at post-operative day 1 (POD1)
Lasso di tempo: Post-operative day 1 (24 hours after surgery)

Postoperative pain intensity is measured using a verbally administered numeric rating scale (NRS) ranging from 0 to 10.

0 indicates no pain while 10 indicates the worst pain that the participant can imagine or has experienced. The score will be recorded as an integer.

The pain scores will be taken from the participants on POD1 between the hours of 08:00 and 12:00. If the participant is discharged, a telephone call will be made during those hours.
Post-operative day 1 (24 hours after surgery)
Average numeric rating scale (NRS) pain score (0-10) at post-operative day 3 (POD3)
Lasso di tempo: Post-operative day 3 (72 hours after surgery)

Postoperative pain intensity is measured using a verbally administered numeric rating scale (NRS) ranging from 0 to 10.

0 indicates no pain while 10 indicates the worst pain that the participant can imagine or has experienced. The score will be recorded as an integer.

The pain scores will be taken from the patients on POD3 between the hours of 08:00 and 12:00. If the participant is discharged, a telephone call will be made during those hours.
Post-operative day 3 (72 hours after surgery)
Average morphine milligram equivalents (MME) in the post-anesthesia care unit (PACU)
Lasso di tempo: PACU arrival to PACU discharge (1-4 hours post-surgery)

Cumulative opioid consumption will be measured using morphine milligram equivalents (MME) which will convert all administered opioids regardless of agent or route of administration to an equivalent amount of oral morphine using standard conversion factors.

Opioid dosage data will be abstracted from the electronic medical record. The total MME administered between the PACU arrival timestamp and the documented PACU discharge-order timestamp will be recorded.

A lower cumulative MME indicates less opioid requirements.
PACU arrival to PACU discharge (1-4 hours post-surgery)
Average morphine milligram equivalents (MME) over the first 24-hour post-operative period
Lasso di tempo: Post-operative day 1 (24 hours after surgery)

Cumulative opioid consumption will be measured using morphine milligram equivalents (MME) which will convert all administered opioids regardless of agent or route of administration to an equivalent amount of oral morphine using standard conversion factors.

Opioid dosage data will be abstracted from the electronic medical record. The total MME administered within the first 24 hours after surgery will be recorded.

A lower cumulative MME indicates less opioid requirements.
Post-operative day 1 (24 hours after surgery)
Proportion of participants experiencing postoperative nausea or vomiting in the post-anesthesia care unit (PACU)
Lasso di tempo: PACU arrival to PACU discharge (1-4 hours post-surgery)

Postoperative nausea or vomiting is defined as any event of nausea or emesis. Episodes will be abstracted from the electronic medical record and corroborated by asking the patient.

Events will be recorded during the PACU stay
PACU arrival to PACU discharge (1-4 hours post-surgery)
Proportion of participants experiencing postoperative nausea or vomiting on post-operative day 1 (POD1)
Lasso di tempo: Post-operative day 1 (24 hours after the surgery)

Postoperative nausea or vomiting is defined as any event of nausea or emesis. Episodes will be abstracted from the electronic medical record and corroborated by asking the patient.

Events will be recorded on POD1
Post-operative day 1 (24 hours after the surgery)
Proportion of participants experiencing postoperative nausea or vomiting on post-operative day 3 (POD3)
Lasso di tempo: Post-operative day 3 (72 hours after the surgery)

Postoperative nausea or vomiting is defined as any event of nausea or emesis. Episodes will be abstracted from the electronic medical record and corroborated by asking the patient.

Events will be recorded on POD3
Post-operative day 3 (72 hours after the surgery)
Proportion of participants who require intra-operative conversion from robotic-assisted surgery to open surgery
Lasso di tempo: During the surgery (about 60 to 240 minutes)
Conversion events will be abstracted from the operative note posted on the electronic medical record.
During the surgery (about 60 to 240 minutes)
Proportion of participants with clinical or radiographic subcutaneous emphysema
Lasso di tempo: From start of surgery to PACU discharge (1-4 hours after surgery)
Cases will be identified by intraoperative inspection of the abdominal wall during the procedure, clinical examination during the PACU stay, and any postoperative imaging that is clinically obtained.
From start of surgery to PACU discharge (1-4 hours after surgery)
Proportion of participants who sustained intraoperative pressure elevation (defined as sustained increase to ≥12 mmHg for ≥10 minutes in the AirSeal arm)
Lasso di tempo: During the surgery (about 60 to 240 minutes)
Pressure measurements will be obtained from the AirSeal console and elevations will be recorded regardless of reason.
During the surgery (about 60 to 240 minutes)

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Weill Medical College of Cornell University

Investigatori

  • Investigatore principale: Cheguevara Afaneh, MD, New York-Presbyterian/Weill Cornell Medical Center

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 luglio 2026

Completamento primario (Stimato)

1 gennaio 2027

Completamento dello studio (Stimato)

1 febbraio 2027

Date di iscrizione allo studio

Primo inviato

13 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

13 luglio 2026

Primo Inserito (Effettivo)

17 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

17 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

13 luglio 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Parole chiave

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • 26-05030301

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

Sì

prodotto fabbricato ed esportato dagli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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