Impact of perioperative use of audiovisual Distraction in patients undergoing orthognathic surgery

Impact of perioperative use of audiovisual Distraction in patients undergoing orthognathic surgery - IDEA

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00030349

Enrollment

Registered

2022-10-05

Start date

2022-12-05

Completion date

Unknown

Last updated

2026-01-12

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

Conditions

EMERGENCE AGITATION

Interventions

Group 1: Procedure for planned monomaxillary surgery (40 patients): Patients in the intervention group will be called off to the OR area approximately one hour prior to the start of general anesthesia

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients undergoing electve orthgnathic surgery at Freiburg University hospital

Exclusion criteria

Exclusion criteria: 1. Absence of informed consent of the patient 2. Age <18years 3. Impaired hearing and/or vision

Design outcomes

Primary

Measure	Time frame
Patients undergoing monomaxillary surgery (40 patients): Level of postoperative agitation measured by the AONO Agitation Scale	—

Secondary

Measure	Time frame
Patients undergoing monomaxillary osteotomy (40 patients): 1. Level of agitation measured by the Richmond Agitation-Sedation Scale 2. Level of preoperative anxiety before induction of general anesthesia 3. Level of postoperative pain 4. Level of postoperative Nausea and vomiting (PONV) 5. Length of stay in the recovery room. 6. Patients satisfaction with anesthesiologic care on the first postoperative day.	—

Measure

Time frame

Patients undergoing monomaxillary osteotomy (40 patients): 1. Level of agitation measured by the Richmond Agitation-Sedation Scale 2. Level of preoperative anxiety before induction of general anesthesia 3. Level of postoperative pain 4. Level of postoperative Nausea and vomiting (PONV) 5. Length of stay in the recovery room. 6. Patients satisfaction with anesthesiologic care on the first postoperative day.

—

Countries

Germany

Contacts

Public ContactMatthias Posch

Klinik für Anästhesiologie und IntensivmedizinUniversitätsklinikum Freiburg

matthias.jakob.posch@uniklinik-freiburg.de0761-27023690 (Sekretariat Anästhesie)

Outcome results

None listed

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