ClinicalTrials.gg
CompletedNCT01231087Updated Nov 1, 2010

Energy Expenditure Pre and Post Bariatric Surgery

An observational study in Bariatric Surgery, sponsored by Gastrocirurgia, Brazil. Completed at 1 site in Brazil. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2010-11-01.

Sponsored by Gastrocirurgia, Brazil · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
32
Ages
18 Years to 75 Years
Sex
All
01

Study summary

Obese patients are going to be submitted to indirect calorimetry pre-operatively and we are going to repeat the same exam 6 months after bariatric surgery (post Roux-en-Y gastric Bypass surgery). They are going to do also body composition analysis in both moments.

The investigators are going to compare the results to see if the bariatric surgery increases their energy expenditure.

02

Conditions studied

  • Bariatric Surgery

Browse trials for

Keywords

  • energy expenditure
  • morbid obesity
  • bariatric surgery
  • nutritional follow-up
03

In context

Obesity, Morbid

936 studies on the registry are indexed under Obesity, Morbid; 169 are open to participants now.

This study's enrollment of 32 is below the median of 77 across 311 observational studies indexed under Obesity, Morbid.

Browse Obesity, Morbid studies →

Lead sponsor

Gastrocirurgia, Brazil is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Obese petiets

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • obese patients that will be submitted to bariatric procedure

Exclusion criteria

Exclusion Criteria:

  • patients that don´t have clinical conditions to be submitted to a bariatric procedure
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
32 participants (actual)
06

Study locations

1 site
  • Gastrocirurgia
    Brasília, Federal District 70390108, Brazil
07

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Jan 2008, a primary completion of Jan 2008 and a completion of Oct 2010. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 29, 2010
First posted
Nov 1, 2010
Start
Jan 2008
Primary completionActual
Jan 2008
CompletionActual
Oct 2010
Last update
Nov 1, 2010
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Nov 1, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT01231087
Lead sponsor
Gastrocirurgia, Brazil
First posted
Nov 1, 2010
Start date
Jan 2008
Primary completion
Jan 2008
Completion
Oct 2010
Last update
Nov 1, 2010

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2010. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion