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Comparison of Sedated and Unsedated PEG in Elderly ASA IV Patients

NCT07758153 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 70

Last updated 2026-08-11

No results posted yet for this study

Summary

This prospective observational cohort study aims to compare the safety and clinical outcomes of sedated and unsedated percutaneous endoscopic gastrostomy procedures in elderly patients classified as ASA IV. The primary outcome is the development of cardiopulmonary complications within the first 24 hours after the procedure. Secondary outcomes include technical success, procedure duration, early procedure-related complications, length of hospital stay, intensive care requirement, 30-day mortality, and 30-day readmission.

Conditions

  • Percutaneous Endoscopic Gastrostomy
  • Enteral Nutrition Feeding
  • Dysphagia
  • Elderly Patients (>65 Years)
  • ASA Physical Status IV

Sponsors & Collaborators

  • Mersin University

    lead OTHER

Eligibility

Min Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-07-15
Primary Completion
2027-06-30
Completion
2027-07-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07758153 on ClinicalTrials.gov