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NCT06432933Completed

Comparison of Apnea-Hypopnea Index in Patients With or Without Preventive Oxygen Therapy After Bariatric Surgery

Comparison of Apnea-Hypopnea Index, in Patients With Potentially Undiagnosed Obstructive Sleep Apnea, Treated With or Without Preventive Oxygen Therapy, During the First Night After Bariatric Surgery

Source: ClinicalTrials.gov · Last updated 18 Jul 2025

Brief summary (registry, in English)

The best perioperative strategy for obstructive sleep apnea (OSA) in bariatric surgery remains unclear. A strategy is to monitor patients and administer preventive oxygen therapy during the first postoperative night. However it is unknown what if preventive oxygen therapy is necessary. The goal of this trial is to compare the Apnea-Hypopnea Index (AHI) in participants with or without preventive oxygen therapy. Methods: Participants are patients who underwent bariatric surgery without treated OSA and will be will be randomized into arm A or arm B: Arm A: First postoperative night in the hospital with preventive oxygen therapy (standard care), Arm B: First postoperative night in hospital without preventive oxygen therapy (intervention).

Status (registry)
Completed
Study type
Interventional
Enrollment
153 (actual)
First submitted
3 Apr 2024
Start date
9 Apr 2024
Primary completion date
21 Mar 2025
Lead sponsor
Rijnstate Hospital
Diseases
Obesity
NCT number
NCT06432933

What you commit to

  • Study type: Interventional
  • Participants enrolled: 153
  • From 9 Apr 2024 to the primary completion date, 21 Mar 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Revisional bariatric surgery (e.g. sleeve conversion, RYGB after gastric banding)
  • Same-day discharge after bariatric surgery

Other

  • Diagnosed OSA with treatment (CPAP, oral appliances)
  • Professional drivers
  • Use of alpha blockers
  • Unable to speak or read the Dutch language

Who the study is looking for

  • Undergo primary bariatric surgery (RYGB or SG)
  • Speak and read the Dutch language

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Vitalys
Coordinator of this site? Confirm its status
ElstNetherlandsUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.