CompletedNot Applicable

I-gel vs. Endotracheal Intubation for Laparoscopic Gynaecological Procedures

Belgium120 participantsStarted 2023-10-11

Plain-language summary

The goal of this interventional study is to compare the I-gel laryngeal mask, a type of supraglottic airway device (SGA), with endotracheal intubation in terms of safety, ease of use and adverse side effects for patients during gynecologic laparoscopic procedures at the Brussels Fertility Center in Brussels, Belgium.

Who can participate

Age range18 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * The expected duration of the procedure does not exceed 2 hours * Agreeing to participate in the study Exclusion Criteria: * The expected duration of the procedure is longer than 2 hours * The patient suffers from restricted mouth opening, trismus, recent oral trauma or oral abscesses * The patient has a BMI of more than 40 kg/m² * The patient is known to have gastroparesis or another risk factor that would prevent you from being sober during the procedure

What they're measuring

Leak fraction

Timeframe: Thirty seconds after placement of the airway device, 30 seconds after completing insufflation of the abdomen, 30 seconds after positioning the patient in 30° Trendelenburg, every 10 minutes Trendelenburg, and 30 seconds after closing the fascia.

Trial details

NCT IDNCT05782517

SponsorUniversitair Ziekenhuis Brussel

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-10-21

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