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AI-generated video-assisted informed consent and patient comprehension in elective otolaryngologic surgery: a randomized controlled trial

AI-generated video-assisted informed consent and patient comprehension in elective otolaryngologic surgery: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00040957
Enrollment
100
Registered
2026-07-15
Start date
2025-09-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Elective ENT surgeries: septoplasty, sinus surgery, tonsillectomy, flexible panendoscopy

Interventions

Group 1: Arm 1 = Standard medical counseling [Control] Group 2: Arm 2 = Standard education + AI video

Sponsors

Asklepios Klinik Harburg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adults (= 18 years) undergoing the following elective procedures: panendoscopy, septoplasty, functional endoscopic sinus surgery (FESS), tonsillectomy, pansinus procedures, and pediatric ENT procedures (tonsillotomy, adenotomy, and placement of ear tubes).

Exclusion criteria

Exclusion criteria: Patients who were scheduled for emergency surgery were excluded.

Design outcomes

Primary

MeasureTime frame
primary endpoint (ICQ total score for items 1–15)

Secondary

MeasureTime frame
secondary endpoints (individual items, recall items)

Countries

Germany

Contacts

Public ContactYano Pöhlmann

Asklepios Klinik Harburg

y.poehlmann@asklepios.com+4940 181886 49 72

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 10, 2026