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Evaluation of motorized spiral endoscopy for the treatment of small bowel diseases, ERCP in surgical altered anatomy and colonoscopy

Evaluation of motorized spiral endoscopy for the treatment of small bowel diseases, ERCP in surgical altered anatomy and colonoscopy - GPS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00026990
Enrollment
1300
Registered
2021-11-09
Start date
2021-11-05
Completion date
Unknown
Last updated
2026-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Angiodysplasia with bleeding K50.0 K83.0 K83.1 D12.0

Interventions

Group 1: All patients with an indication for a device-assisted endoscopy in which a motorized spiral enteroscopy is the selected device. Data shall be collected from the intervention itself (motorized

Sponsors

Viszeralmedizinisches Zentrum, Evangelisches Diakoniekrankenhaus Freiburg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: age = 18 years, indication for device-assisted endoscopy (DAE) (= suspected or known small bowel pathology with the need of a DAE for further diagnostics or therapy, indication for an ERCP in surgical altered anatomy of the gastrointestinal tract (for example status Y-Roux reconstruction, batriatic surgery) without a different possibility of retrograde access to the biliary tract with conventional endoscopy, completion of an incomplete standard colonoscopy), willingness and possibility to participate in the follow up of the study, present oral and written informed consent for the participitation in the registry.

Exclusion criteria

Exclusion criteria: incapacitated patient, pregnancy, ASA-Score V

Design outcomes

Primary

MeasureTime frame
For indication small bowel disease: complete enteroscopy. For indication biliary disease in surgical altered anatomy: technical success of ERCP. For indication incomplete colonoscopy: successful cecal intubation.

Secondary

MeasureTime frame
For indication small bowel disease: type of complete enteroscopy (only peroral/peranal or peroral+peranal access), intention of complete enteroscopy, technical success, depth of insertion, type of access (peroral or peranal), use of fluoroscopy, in case of bidirectional access order and chronological sequence of procedures. For indication biliary disease in surgical altered anatomy: way of access (peroral or peranal), length of afferent loop. For indication incomplete colonoscopy: use of fluoroscopy. All indications: indication, preliminary examinations, results of preliminary examinations, time of insertion, intervention, withdrawal and whole examination, definitive diagnosis and type of definitive diagnosis, therapeutic intervention and type of therapeutic intervention, adverse events, serious adverse events, type of complications, therapy of complications, outcome of complications, preliminary surgery of the (small) bowel, use of intubation anesthesia, number of involved personnel, type of instruments, technical difficulties and type of technical difficulties, the reason and alternative procedure in case of technical failure, level of difficulty, use of a distal cap. Telephone interview (follow-up) for all indications: complications, outcome of the primary disease.

Countries

Germany

Contacts

Public ContactIngo Steinbrück

Viszeralmedizinisches Zentrum, Evangelisches Diakoniekrankenhaus Freiburg

ingo.steinbrueck@diak-fr.de0761130193355

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 7, 2026