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Clinical Trials/DRKS00019850
DRKS00019850
Completed
N/A

The influence of different surgical interventions on neural food cue reactivity in obese patients - Obelix 2

Zentralinstitut für Seelische Gesundheit Mannheim0 sites26 target enrollmentNovember 26, 2019
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ConditionsE66Obesity

Overview

Phase
N/A
Intervention
Not specified
Conditions
E66
Sponsor
Zentralinstitut für Seelische Gesundheit Mannheim
Enrollment
26
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 26, 2019
End Date
November 26, 2014
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Zentralinstitut für Seelische Gesundheit Mannheim

Eligibility Criteria

Inclusion Criteria

  • •For all study participants
  • •\- age between 18 and 65 years,
  • •\- the capacity to give informed consent and to handle the questionnaires
  • •\- written informed consent
  • •For patients:
  • •\- BMI (kg/m2\) \> 35 (\= grade 2 obesity) according to the ICD\-10
  • •\- waist circumference \< 160 cm (limited by scanner diameter)

Exclusion Criteria

  • •\-withdrawal of informed consent
  • •\- history or current diagnosis of any psychiatric disorder, (with the exception of nicotine addiction) that needed to be treated pharmacologically in the last 12 months
  • •\- current cognitive behavioral therapy
  • •\- current use of illicit drugs
  • •\- current suicidal ideation
  • •\- history of brain injury or severe neurological disorder
  • •\- current instable somatic disorder
  • •\- current intake (last 4 months) of any centrally acting psychoactive or anti\-obesity medications (i.e. sedatives, antipsychotics, including long\-acting injectable antipsychotics, antidepressants, opioid analgesics as well as DPP (dipeptidyl peptidose IV) inhibitors and GLP (Glucagon\-like peptide)\-1 antagonists,
  • •\- all participants with a history of surgical interventions in the gastrointestinal system
  • •\-all participants requiring permanent medical monitoring or requiring medical interventions during the study period

Outcomes

Primary Outcomes

Not specified

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