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Determination of risk factors for complications that may occur when endoscopic gastrostomy is performed for dietary intake in patients with amyotrophic lateral sclerosis

Risk factor for complication of percutaneous endoscopic gastrostomy in patients with amyotropic lateral sclerosis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0010478
Enrollment
161
Registered
2025-05-20
Start date
2025-05-02
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

None listed

Interventions

None listed

Sponsors

Hanyang University Seoul Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who were diagnosed with ALS and underwent PEG at our hospital from December 2002 to December 2024 are eligible, and only patients undergoing PEG insertion for the first time are eligible.

Exclusion criteria

Exclusion criteria: 1) PEG tube change (if the procedure was performed using an existing gastrostomy tract from a previous procedure), 2) Balloon type PEG insertion, 3) Excluding patients who underwent the procedure more than twice even if PEG was performed using a new gastrostomy tract, 4) poor record keeping, short follow-up period (within 1 month)

Design outcomes

Primary

MeasureTime frame
complication; (1) bleeding, (2) infection, (3) necrotizing fasciitis, (4) peritonitis, (5) perforation, (6) buried bumper syndrome, (7) tube dislodgement, (8) intramural hematoma of esophagus, (9) pneumoperitoneum with symptoms, (10) injury to adjacent organ, (11) peristomal infection. All listed complications are combined and evaluated as a single variable called complications.

Countries

Korea, Republic of

Contacts

Public ContactJin Hwa Park

Hanyang University Seoul Hospital

pjh6718@hanmail.net+82-2-2290-8303

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026