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NCT06853652Recruiting

Protein Requirements After Bariatric Surgery

Maintenance-phase PROtein Requirements After RouX-en-Y-gastric Bypass Surgery

Source: ClinicalTrials.gov · Last updated 3 Mar 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The study investigates protein requirements at least 1 year after gastric bypass surgery in adult males, to investigate whether protein requirements are elevated compared to protein requiremens for the general populaiotn. The main study outcome is the estimated average protein requirements for the study populaiton.

Status (registry)
Recruiting
Study type
Observational
Enrollment
20 (estimated)
First submitted
21 Feb 2025
Start date
17 Mar 2025
Primary completion date
25 Jun 2026
Lead sponsor
Universitaire Ziekenhuizen KU Leuven
Diseases
Obesity
NCT number
NCT06853652

What you commit to

  • Study type: Observational
  • Planned participants: 20
  • From 17 Mar 2025 to the primary completion date, 25 Jun 2026
  • 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

  • Weight loss after bariatric surgery of less than 40% of excess weight,
  • Weight regain after bariatric surgery greater than 20% of nadir weight,

Other illness

  • Current diagnosis of cancer or active cancer in the preceding 1 year,
  • Any chronic or acute disease which is known to affect amino acid absorption, metabolism, or requirements,

Lab values

  • Diabetes mellitus defined as a fasting plasma glucose concentration ≥ 7.0 mmol, or HbA1c less than 6.5%, or medical treatment for diabetes.

Who the study is looking for

  • Male aged 18 - 65 years,
  • Primary RYGB surgery one to ten years before,
  • Weight stable within 5% over the last 3 months,
  • Normotensive or blood pressure controlled with antihypertensive therapy,
  • Provision of informed consent to participate,

Age in the registry: 18 years to 65 years · Sex: Male · Does not accept 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
Universitaire Ziekenhuizen KU Leuven
Coordinator of this site? Confirm its status
LeuvenBelgiumRecruiting

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