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Influence of the Sleep Pattern in Patients Submitted to Bariatric Surgery

F

Federal University of Uberlandia

Status

Completed

Conditions

Bariatric Surgery Candidate

Study type

Observational

Funder types

Other

Identifiers

NCT03485352
CEP UFU 2459483/2017

Details and patient eligibility

About

The present study has a prospective, longitudinal and observational character, will be performed with patients attending a private clinic specialized in the treatment of obesity and bariatric surgery. Patients to be analyzed should have a medical indication for bariatric surgery.

Full description

The patients will be selected for ten months and will be monitored for 12 months there are preoperative period, 3 months, 6 months and 12 months after surgery. Anthropometrical evaluation, biochemistry, polysomnography and sleep questionnaire (Epworth and Psqi) and midpoint sleep questionnaires will be performed to classify the chronotype for sleep pattern evaluation.

Enrollment

122 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Agree to participate in the study and sign the Informed Consent Form (EHIC)
  • Patients submitted to By-pass or Sleeve bariatric surgery or Endossleve
  • Patients with BMI above 35 kg / m².
  • Over the age of 18 and up to 60 years.

Exclusion criteria

  • Failure to provide the information necessary for the development of the study.
  • Patients undergo revisional surgery

Trial design

122 participants in 1 patient group

Bariatric Surgery patients
Description:
Patients attending a private clinic specialized in the treatment of obesity and bariatric surgery. Patients to be analyzed should have a medical indication for bariatric surgery.

Trial documents
3

Trial contacts and locations

1

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Central trial contact

Cibele A Crispim, PhD

Data sourced from clinicaltrials.gov

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