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NCT07417683Not yet recruiting

Multicentric Approval Study Trans-Duodenal Barrier for Typ 2 Diabetes With Obesity

Leistung Und Sicherheit Des Trans-Duodenal Barrier (LuST)

Source: ClinicalTrials.gov · Last updated 18 Feb 2026

Brief summary (registry, in English)

Approval study Trans-Duodenal Barrier The goal of this clinical trial is to determin the safety and performance of the newly developed Trans-Duodenal Barrier in adult Tryp 2 diabetic and obese patients. The Trans-Duodenal Barrier is an endoscopic implant which can be placed to the gastric outlet and the upper small bowel by interventional endoscopy. It consists of a 60 cm long foil tube , a transpyloric shaft and and two ringlike balloons to fix it at the pylorus. It will be removed after 6 months via gastroscopy. The main questions it aims to answer are: * Does the Trans-Duodenal Barrier lower the HbA1c of the participants ? * How frequent are adverse side effects related to the device? * How much ist the excessive wight loss of treated patients ? * Show patients with Metabolic assiociated Hepatosteatitis (MASH) improvements in liver elasticity (elastography) ? Researchers implant the Trans-Duodenal Barrier to enclosed patients and follow up them till 4 weeks after explantation. Participants will: * Get the Trans-Duodenal Barrier as an implant for 6 moths * Visit the clinic 3 times in the implant period and once for explant. * Receive a telefon interview 4 weeks after explant

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
126 (estimated)
First submitted
10 Feb 2026
Start date
1 Mar 2026
Primary completion date
31 Mar 2028
Lead sponsor
Trans-Duodenal Concepts GmbH
NCT number
NCT07417683

What you commit to

  • Study type: Interventional
  • Planned participants: 126
  • From 1 Mar 2026 to the primary completion date, 31 Mar 2028
  • 8 sites 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.

Other illness

  • The patient is participating in another clinical trial in the field of diabetes management or metabolic syndrome.

Other

  • The patient is mentally incapable of understanding the nature, objectives, or possible consequences of the clinical trial.
  • The patient is unwilling or unable to follow postoperative instructions.
  • The patient has been placed in an institution by court order or official order (MPDG §27).
  • The patient lives more than 100 km from the treatment site.
  • Pregnancy.

Who the study is looking for

  • Obese patients with type 2 diabetes mellitus,
  • Age ≥ 18 years,
  • The patient is able to understand the nature, significance, and scope of the clinical trial (MPDG §28),
  • The patient has been informed and all written consents from the patient are available.

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

Full criteria on ClinicalTrials.gov

Sites (8)

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

SiteCityCountrySite status
Sozialstiftung Bamberg
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BambergGermanyUnknown status
Charite Universitätmedizin Berlin CVK
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BerlinGermanyUnknown status
Knappschaft Kliniken Universitätsklinikum Bochum GmbH Medizinische Klinik
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BochumGermanyUnknown status
Städtisches Klinikum Dresden
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DresdenGermanyUnknown status
University of Leipzig Medical Center, Department of Oncology, Gastroenterology, Hepatology and Pneumology
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LeipzigGermanyUnknown status
Klinikum St. Georg Leipzig
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LeipzigGermanyUnknown status
Universitätsmedizin Mannheim
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MannheimGermanyUnknown status
Universitätsklinikum Würzburg
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WürzburgGermanyUnknown status

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