Viewing Study NCT05743166


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Study NCT ID: NCT05743166
Status: RECRUITING
Last Update Posted: 2025-06-05
First Post: 2023-02-14
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Bariatric Surgery Observation Study Part 2
Sponsor: St. Olavs Hospital
Organization:

Study Overview

Official Title: Bariatric Surgery Observation Study Part 2 An Observational Study of Patients Who Underwent Bartiatric Surgery in Public Hospitals in Central Norway 2010-2015.
Status: RECRUITING
Status Verified Date: 2025-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: BAROBS2
Brief Summary: The goal of this observational study is to explore the longterm effects of two bariatric surgical procedures by inviting patients from three public hospitals who had Roux-en-Y gastric bypass or Sleeve gastrectomy to a follow-up after10-15 years

The main question\[s\] it aims to answer are:

* The duration of the surgical method on weight reduction and remission of comorbidities
* Theprevalence of complications and new morbidities after the surgical procedures Participants will be asked be asked to

* fill inn questionnaires,
* have a clinical examinition
* have an interview with nurse and doctor
* have blood samples taken
* undergo other investigations
Detailed Description: The BAROBS project is a collaberation between three public hospitals in Norway exploring the concequeces ten years or more after undergoing gastric bypass or sleeve gastrectomy for severe obesity.

1400 patients who underwent bariatric surgery at the three hospitals will be invited to a follow up including antrophometric, meassurment of bodily composition by bioimpedance and DXA, blood samples, questionnaires on sosioeconomic topics, symptoms and quality of life, continous glucose monitoring, dental examination, and other clinical evaluation.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: