Patient Experience With OMS Procedures Regarding Anesthesia

East Limburg Hospital

Status: Completed

Conditions: Patient Satisfaction

Treatments: Other: Questionnaire

Study type: Interventional

Funder types: Other

Identifiers

NCT04863599

Z-2021038

Details and patient eligibility

About

The main purpose of the study is to know more about the experience/satisfaction of patients undergoing oral and maxillofacial surgery (OMS). Depending on the type of procedure, the patient will receive a sedation or a general anesthesia. At the first day post-operatively, patients will be contacted to complete a questionnaire. The questionnaire will be subdivided into anaesthesia-related discomfort and anaesthesia care in general.

Enrollment: 178 patients

Sex: All

Ages: 12+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• OMS procedure
• signed informed consent
• Age above 12 years

Exclusion criteria

• need for post-operative hospitalization
• mental disorder with no capability of filling in questionnaires

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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178 participants in 1 patient group

OMS procedure under general anesthesia or sedation

Other group

Description:

Questionnaire

Treatment:

Other: Questionnaire