Patient-Controlled Anesthesia for endoscopic Procedural Sedation – PCAPS study

Status

Not yet recruiting

Phases

Phase 4

Study type

Interventional

Source

EU CTIS

Registry ID

CTIS2025-524859-31-00

Enrollment

175

Registered

2026-08-11

Start date

Unknown

Completion date

Unknown

Last updated

2026-08-11

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

Conditions

Adenoma

Brief summary

Patient satisfaction measured using a validated questionnaire

Detailed description

Total dose of propofol delivered (mg), Procedure time, Recovery time, Adverse events, Procedure completion rate

Interventions

DRUGPROPOFOL

DRUGALFENTANIL

DRUGMIDAZOLAM

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Design outcomes

Primary

Measure	Time frame
Patient satisfaction measured using a validated questionnaire	—

Secondary

Measure	Time frame
Total dose of propofol delivered (mg), Procedure time, Recovery time, Adverse events, Procedure completion rate	—

Outcome results

None listed

Source: EU CTIS · Data processed: Aug 12, 2026