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Prospective randomized controlled study for evaluation of an Augmented Reality Pointer for optimzing surgical education

Prospective randomized controlled study for evaluation of an Augmented Reality Pointer for optimzing surgical education - APACHE

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00029209
Enrollment
32
Registered
2022-06-08
Start date
2019-07-19
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

K80

Interventions

Group 1: Intervention group - use of the HoloPointer The lap. CHE is performed according to the standard. In addition, the surgeon and assisting surgeon wear a HoloLens and can use it to display a po

Sponsors

Klinik für Allgemein-, Viszeral- und Transplantationschirurgie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: planned elective laparoscopic cholecystectomy, operation by resident, non privately insured, 4 port technique

Exclusion criteria

Exclusion criteria: emergency operation, planned open procedure, privately insured, 3 port technique

Design outcomes

Primary

MeasureTime frame
Effect of an AR pointer on the quality of the surgical training in laparoscopic cholecystectomy (critical view of safety, GOALS and subjective evaluation)

Secondary

MeasureTime frame
Influence on the learning success/understanding of assistants (with AR pointer vs. without AR Pointer) Influence on the satisfaction of the trainer with the skills of the Trainee (with AR pointer vs. without AR Pointer) Impact on operation time (with AR pointer vs. without AR Pointer) Influence on peri- and postoperative complications (with AR pointer vs. without AR pointer)

Countries

Germany

Contacts

Public ContactTobias Huber

Klinik für Allgemein-, Viszeral- und Transplantationschirurgie, Universitätsmedizin der Johannes Gutenberg-Universität Mainz

tobias.huber@unimedizin-mainz.de0049 6131 17 3613

Outcome results

None listed

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