Risk acceptation of morbidly obese patients seeking weight loss surgery

Completed

• Conditions: Morbide Obesitas en bariatrische chirurgie; Morbid obesitas; 10003018; 10017998

• Registration Number: NL-OMON47496
• Lead Sponsor: MC Slotervaart

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 200

Inclusion Criteria

Age 18-65
Seeking weight loss surgery
written informed consent

Exclusion Criteria

Incapability to complete Dutch questionnaires or to engage in a Dutch interview due to insufficient ability to understand or speak the Dutch language
No written informed consent

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Main study parameter is the maximum accepted risk on serious adverse events<br /><br>(<30 days).</p><br>

Secondary Outcome Measures

Name	Time	Method
<p> Secondary study parameters are expected weight loss and maximum accepted risk<br /><br>on mortality, long-term complications and side effects and associations with<br /><br>specific patient characteristics.</p><br>