Quality of Life and Cardiometabolic Risk Factors in Patients After Debanding

Follow up of debanding patients

Completed

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Key information

Conditions

Bariatric Patients

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University Hospital of Zurich

Zurich, Switzerland

About this study

Follow up of debanding patients regarding cardiometabolic risk factors

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Previous debanding after lap. gastric bypass

Exclusion criteria

Further bariatric procedures

Treatment and study plan

Primary outcomes

Quality of Life

Time frame: 2 to 5 years after debanding

Sponsors and collaborators

Lead sponsor

University of Zurich

Other

Collaborators

Cantonal Hospital, Frauenfeld

Registry information

Important dates

Study start: 2007
Primary completion: 2015
Study completion: 2015
First posted: Jul 6, 2007
Registry last updated: May 12, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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Completed