Colonoscopy Procedure

2

Review clinical trials related to Colonoscopy Procedure. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Patient Controlled Propofol Sedation Versus Nurse-assisted Propofol Sedation in Diagnostic Colonoscopies With a Focus on Patient Satisfaction

The goal of this clinical trial is to learn if patient administered propofol sedation results in superior patient satisfaction compared to nurse administered propofol sedation in diagnostic colonoscopies. • Does self administration of the sedative propofol increase patient satisfaction? Researchers will compare patient administered propofol sedation (where the patient administers propofol by pushing a button) with nurse administered propofol sedation (where a nurse gives the patient bolus doses of propofol as deemed necessary) Participants will: * Be randomized to either sedation route. * Answer a preendoscopy questioneere and a postendoscopy questioneere 1 hour after the examination as well as one week after the examination.

Participants needed: 135
Trial details
Phase: Phase 4Age: 18-90Biological sex: AllType: InterventionalSponsor: Karolinska InstitutetUpdated: Jun 17, 2026Locations: 2
Eligibility criteria

Scheduled for elective diagnostic colonoscopy in propofol sedation [+4]

ASA >=III [+6]

Status: Not yet recruiting

Use of GI Genius™ XR Software in Virtual Reality Headset During Routine Colonoscopy

This pilot study will evaluate the usability and safety of software GI Genius™ XR in the Apple Vision Pro™ virtual reality headset when used in conjunction with the GI Genius™ system during routine screening and surveillance colonoscopy procedures. GI Genius™ XR enables colonoscopists to view the standard live endoscopic video feed within a virtual reality environment as an alternative to the conventional endoscopy tower display. The system provides a virtual screen that mirrors the tower video output without any image analysis or interpretation, allowing users to adjust screen size and position for optimal visualization and situational awareness.

Participants needed: 15
Trial details
Age: 45+Biological sex: AllType: InterventionalSponsor: Cosmo Artificial Intelligence-AI LtdUpdated: Oct 23, 2025Locations: 1
Eligibility criteria

Male or female aged ≥ 45 years; [+4]

Not able to comply with the protocol requirement; [+11]