Evaluation of complication rates of two licensed percutaneous endoscopic gastrostomy tubes in direct puncture technique

Evaluation of complication rates of two licensed percutaneous endoscopic gastrostomy tubes in direct puncture technique - COMPLIPEG-DP

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

DRKS

Registry ID

DRKS00027256

Enrollment

235

Registered

2021-12-03

Start date

2021-12-12

Completion date

Unknown

Last updated

2026-03-02

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

Conditions

enteral feeding

Interventions

Group 1: use of Freka Pexact II Group 2: use of Nutricia Milupa FLOCARE DirectPEG

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: All patients with indication for PEG

Exclusion criteria

Exclusion criteria: Patients with ongoing anticoagulation, missing transillumination during gastroscopy, contraindication for PEG

Design outcomes

Primary

Measure	Time frame
Complication rate within 30 days	—

Secondary

Measure	Time frame
Time of procedure, handling of the devices, patency of PEG tube, dislocation rate within 30 days	—

Countries

Germany

Contacts

Public ContactClaudio C. Conrad

Universitätsklinikum Schleswig-Holstein Klinik für Innere Medizin I

claudiocim.conrad@uksh.de043150022373

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 14, 2026