Status:

COMPLETED

Evaluation of a Telemedicine System for Patients Carried for Bariatric Surgery

Lead Sponsor:

IHU Strasbourg

Conditions:

Bariatric Surgery Candidate

Eligibility:

All Genders

18-65 years

Phase:

NA

Brief Summary

This study is intended to study the feasibility of a telemedicine system to monitor and control certain vital parameters before and after surgery for obesity. During the preoperative preparation phase...

Detailed Description

The evolution of the health system requires a rationalization of the supply of care and the care of patients. It has allowed the evolution and generalization of ambulatory surgery for certain patholog...

Eligibility Criteria

Inclusion

  • Patient (s) applying for bariatric surgery
  • Patient aged 18 to 65
  • Compliance with the High Authority of Health (HAS) criteria:
  • BMI\> 40 without comorbidities
  • BMI\> 35 with cardiovascular, metabolic, respiratory or rheumatic comorbidity,
  • Psychological follow-up well followed for 4 to 6 months
  • Patient with an ASA (American Society of Anesthesiologists) score less than or equal to 2
  • Patient able to receive and understand information about the study
  • Patient able to manipulate connected objects
  • Patient (e) affiliated to the French social security system
  • Patient who does not live in the white area of wireless telephone coverage.

Exclusion

  • Patient unable to give informed consent
  • Patient unable to use the connected tools (Internet)
  • Patient whose general condition is not favorable to participation in the study
  • Patient presenting, in the opinion of the investigator, a condition that may prevent participation in the procedures provided for in the study
  • Patient in exclusion period (determined by previous or current study)
  • Patient under the protection of justice
  • Patient under guardianship or trusteeship
  • Patient with epilepsy
  • Patient who is sensitive to light flashes
  • Patient with deformity of the ear
  • Patient with bleeding ear
  • Exclusion Criteria :
  • Patient whose home is in a white GSM (Global System for Mobile Communications) zone or white zone in reception and 3G (third generation) transmission
  • Patient (e) not knowing how to use connected objects.

Key Trial Info

Start Date :

April 15 2019

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

August 31 2020

Estimated Enrollment :

24 Patients enrolled

Trial Details

Trial ID

NCT03834181

Start Date

April 15 2019

End Date

August 31 2020

Last Update

February 10 2021

Active Locations (1)

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Service de Chirurgie Digestive et Endocrinienne, NHC

Strasbourg, France, 67 091