Perioperative anxiety levels in patients receiving i.v. sedation with midazolam, nitrous oxide sedation and under local anesthesia

Perioperative anxiety levels in patients receiving i.v. sedation with midazolam, nitrous oxide sedation and under local anesthesia - Mid_Anst

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00032254

Enrollment

475

Registered

2023-08-25

Start date

2023-08-28

Completion date

Unknown

Last updated

2025-10-06

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

Conditions

dental axiety

Interventions

Group 1: local anestheaia, intra veinous, nitrous oxide

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Patients of the Department for Dental Surgery and Implantology (2) Mastery of the German language (3) Consent to participate in the study (4) ASA - Class I and II (5) Patient age >= 18 years

Exclusion criteria

Exclusion criteria: (1) No written consent to study (2) ASA - Class III and IV

Design outcomes

Primary

Measure	Time frame
Difference in the pre- and postoperative anxiety level in the therapy groups with and without midazolam based on the MDAS score	—

Secondary

Measure	Time frame
-Comparison of MDAS, HAF and VAS scores -Amount of midazolam, nitrous oxide and/or local anesthetic depending on preoperative anxiety level -Amount of postoperative analgesic in relation to preoperative anxiety level -NRS for pain -Time and human resources in the 3 patient collectives.	—

Countries

Germany

Contacts

Public ContactFrank Schwarz

ZZMK der Goethe-Universität Frankfurt am Main, Poliklinik für Zahnärztliche Chirurgie und Implantologie

a.begic@med.uni-frankfurt.de069-6301-7530

Outcome results

None listed

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