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NCT04242524Completed

The Impact of Bariatric Surgery on Adipocyte Metabolism

Source: ClinicalTrials.gov · Last updated 13 Feb 2026

Brief summary (registry, in English)

The purpose of this study is to understand how daily rhythms of behavior affect the expression of genes in fat cells, and how these daily cycles affect the way fat cells respond to insulin (a hormone that controls blood sugar levels) before and after bariatric surgery.

Status (registry)
Completed
Study type
Interventional
Enrollment
28 (actual)
First submitted
23 Jan 2020
Start date
26 Mar 2015
Primary completion date
15 Dec 2025
Lead sponsor
University of Chicago
Diseases
Obesity
NCT number
NCT04242524

What you commit to

  • Study type: Interventional
  • Participants enrolled: 28
  • From 26 Mar 2015 to the primary completion date, 15 Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Subjects will not have undergone surgery, donated a unit of blood, or participated in another clinical study within the last 4 weeks prior to consent.
  • Subjects will not have undergone surgery, donated a unit of blood, or participated in another clinical study within the last 4 weeks prior to consent.

Other illness

  • Diagnosed with a systemic illnesses, including heart, renal, liver, or malignant disease
  • Uncontrolled hypertension (blood pressure greater than 140 mmHg systolic and 90 mmHg diastolic without medication)
  • known allergy to lidocaine
  • Diagnosed with a systemic illnesses, including heart, renal, liver, or malignant disease
  • Uncontrolled hypertension (blood pressure greater than 140 mmHg systolic and 90 mmHg diastolic without medication)
  • known allergy to lidocaine

Lab values

  • hemoglobin less than 11.5g/dL
  • hemoglobin less than 11.5g/dL

Other

  • Male
  • use of beta blockers
  • pregnancy
  • lactation
  • Post-menopausal
    • Non-Obese Subjects
  • Male
  • use of beta blockers
  • pregnancy
  • lactation
  • Post-menopausal

Who the study is looking for

  • 18-55 years old
  • Female
  • BMI greater than 40 kg/m2
  • Scheduled for bariatric surgery at the Center for the Surgical Treatment of Obesity at the University of Chicago
  • Signed informed consent
  • 18-55 years old
  • Female
  • BMI less than 30 kg/m2
  • Signed informed consent

Criteria the registry did not label

  • Obese Subjects

Age in the registry: 18 years to 55 years · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Chicago
Coordinator of this site? Confirm its status
ChicagoUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.