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PEG by Introducer Method Via EG Scan

T

The Catholic University of Korea

Status

Unknown

Conditions

Esophageal Stenosis
Dysphagia
Aspiration

Treatments

Procedure: Percutaneous Endoscopic Gastrostomy

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT02183207
PEG by EG Scan

Details and patient eligibility

About

Percutaneous endoscopic gastrostomy(PEG) by introducer method has been proven to be safe and easy to perform. However, it is limited by its need to be performed in an endoscopy unit. E.G. ScanTM is an new portable ultrathin endoscope, capable of being performed in any hospital setting and introduced via nasal approach. Our aim is to prove that PEG by introducer method via E.G. ScanTM is feasible and safe. This will allow PEG to be done at hospitals and medical facilities without endoscopic units.

Enrollment

24 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Require percutaneous endoscopic gastrostomy placement due to inability to achieve oral feeding for at least one month

Exclusion criteria

  • Patients with esophageal ulcers or strictures
  • Patients with prior esophageal/gastric surgery (excepting gastric wedge resection)
  • Patients at high risk of gastric bleeding, mechanical ileus or gastrointestinal perforation
  • Other patients in whom the study investigators consider unfit for inclusion

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

24 participants in 1 patient group

PEG insertion arm via EG Scan
Experimental group
Description:
Percutaneous endoscopic insertion of gastrostomy via visualization through E.G. ScanTM
Treatment:
Procedure: Percutaneous Endoscopic Gastrostomy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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