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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03056937
Other study ID # CAAE: 51573315.7.0000.5322
Secondary ID
Status Recruiting
Phase N/A
First received February 14, 2017
Last updated February 14, 2017
Start date February 1, 2016
Est. completion date December 1, 2018

Study information

Verified date February 2017
Source University of Cruz Alta
Contact Carine C Callegaro, PhD
Phone +55 (55) 99914-6712
Email ccallegaro@unicruz.edu.br
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The hypothesis of this study is that reductions in body weight could improve inspiratory muscle function attenuating the inspiratory metaboreflex in metabolically healthy obese individuals and obese individuals with metabolic syndrome.


Description:

Introduction: Peripheral metaboreflex activation appears to be exacerbated in obese individuals with metabolic syndrome. Interestingly, bariatric surgery attenuates the peripheral metaboreflex. Obese individuals have impaired inspiratory muscle function, which can be reversed by the reduction in body weight. Therefore, bariatric surgery could attenuate inspiratory metaboreflex in metabolically healthy obese individuals and obese individuals with metabolic syndrome. Objectives: To investigate the effects of bariatric surgery on inspiratory metaboreflex in metabolically healthy obese individuals and in obese patients with metabolic syndrome. Patients and Methods: A sample comprising of 15 obese subjects with metabolic syndrome, 15 obese subjects without metabolic syndrome and 15 healthy nonobese individuals. These subjects will be submitted to pulmonary function, respiratory muscle strength, inspiratory muscle resistance, exercise tolerance, quality of life, autonomic cardiovascular control and the inspiratory metaboreflex evaluation. The evaluations performed in obese patients with and without metabolic syndrome pre-surgery will be repeated 6 months after bariatric surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 45
Est. completion date December 1, 2018
Est. primary completion date December 1, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 45 Years
Eligibility Obese with Metabolic Syndrome

Inclusion Criteria:

- Body mass index (BMI)> 35 kg / m²

- Diagnosis of metabolic syndrome

Exclusion Criteria:

- Acute health problems in the last month (viral or bacterial infections, accidents, allergic reactions)

- Diseases of the nervous system or conditions that affect the understanding or participation in the study

- Pregnancy

- Type I diabetes mellitus

- Arterial hypertension

- Dyslipidemias

- Coronary artery disease

- Left ventricular dysfunction

- Any condition interfering with locomotion

- Bronchial asthma

- Chronic obstructive pulmonary disease

- Chronic neuropathies

- Use of drugs such as corticosteroids or bronchodilators

- Smokers.

Obese without Metabolic Syndrome

Inclusion Criteria:

- Body mass index (BMI)> 35 kg / m²

Exclusion Criteria:

- Metabolic Syndrome

- Acute health problems in the last month (viral or bacterial infections, accidents, allergic reactions)

- Diseases of the nervous system or conditions that affect the understanding or participation in the study

- Pregnancy

- Type I diabetes mellitus

- Arterial hypertension

- Dyslipidemias

- Coronary artery disease

- Left ventricular dysfunction

- Any condition interfering with locomotion

- Bronchial asthma

- Chronic obstructive pulmonary disease

- Chronic neuropathies

- Use of drugs such as corticosteroids or bronchodilators

- Smokers.

Healthy nonobese subjects

Inclusion Criteria:

- BMI <25 kg / m²

Exclusion Criteria:

- Non-smokers

- Any diagnosed disease.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Bariatric surgery
evaluations pre and post bariatric surgery.
Control
without intervention, it will be performed only evaluations

Locations

Country Name City State
Brazil University of Cruz Alta Cruz Alta Rio Grande do Sul

Sponsors (1)

Lead Sponsor Collaborator
University of Cruz Alta

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Inspiratory metaboreflex It will be induced through a linear inspiratory resistance of 60% of maximal inspiratory pressure 6 monhs
Secondary Pulmonary function It will be assessed by spirometry 6 months
Secondary Respiratory muscle strength It will be determined by manovacuometry. 6 months
Secondary Inspiratory muscle resistance It will be evaluated through a protocol with progressive increase in inspiratory resistance. 6 months
Secondary Autonomic cardiovascular control It will be determined by spectral analysis 6 months
Secondary Exercise tolerance It will be determined by the 6-minute walk test. 6 months
Secondary Quality of life It will be determined through the SF36 questionnaire. 6 months
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