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NCT06865365Not yet recruitingPhase 4

Preoperative Use of Liraglutide Additionally to Common Dietological Measures as Opposed to Dietological Measures Alone

Prospective, Randomized, Controlled Trial of Preoperative Use of Saxenda (Liraglutide) Additionally to Common Dietological Measures as Opposed to Dietological Measures Alone

Source: ClinicalTrials.gov · Last updated 21 Mar 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The aim of the study is to investigate the effects of preoperative Saxenda (liraglutide). There are two groups, one group receives Saxena in addition to dietary measures when first seeking the operation, one group only diet. The investigator is researching how much additional preoperative weight loss is possible with the drug admitted preoperatively.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
72 (estimated)
First submitted
23 Jan 2025
Start date
1 May 2025
Primary completion date
1 Feb 2027
Lead sponsor
Medical University of Vienna
Diseases
Obesity
NCT number
NCT06865365

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 72
  • From 1 May 2025 to the primary completion date, 1 Feb 2027
  • No sites listed in no 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

  • Patients with previous bariatric surgerys
    • Patients aged below 18 years
    • Patients with BMI \< 35 kg/m2
    • Patients with psychiatric disorders
    • Patients not willing to adhere to preoperative dietological measures
    • Patients with contraindications against Saxenda
    • Patients who have health insurance other than Österreichische Gesundheitskasse

Who the study is looking for

  • \- Patients seeking bariatric surgery
  • BMI \> 35.0 kg/m2
  • Health insurance via Österreichische Gesundheitskasse
  • Willingness to be assigned to either of the two groups
  • Willingness to adhere to preoperative dietological measures
  • Follow-up anticipation with blood draws and body weight scans using Secca scale
  • Written informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

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