Menu
Recruiting NCT03200964

OS Anesthesia Followup of All Bariatric Procedures at One Hospital

Observational Anesthesia Recovery

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: anesthesia given as required for surgical procedure.
Who it may be relevant to
Registry conditions: Anesthesia Recovery. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Belgium
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Retrospective Analysis of Anesthesia Delivering for Bariatric Surgery

Overview

Database registering demographic patient data, anesthesia and surgery information, post operative recovery and complications if any.

Detailed description

Every patient undergoing a bariatric procedure is entered in the data base after the procedure is finished, based on the information available in the medical records.

the study has no end point and keeps collecting data as long as procedures are performed.

The data is analyzed intermittent when medical questions arise on quality and outcome changes due to changes in clinical treatment taken in order to improve individual patient care.

Interventions

  • Other anesthesia given as required for surgical procedure

Primary outcome measures

  • Postoperative complications first month after surgery. [Time frame: one month followup]

Eligibility criteria

Inclusion criteria

  • all bariatric procedures

Exclusion criteria

  • none

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Belgium · 1 center
  • Azsintjan — Bruges

Identifiers

NCT: NCT03200964 · OS bariatric database

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗