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Patient Experience With OMS Procedures Regarding Anesthesia

Not Applicable
Completed
Conditions
Patient Satisfaction
Interventions
Other: Questionnaire
Registration Number
NCT04863599
Lead Sponsor
Ziekenhuis Oost-Limburg
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
178
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
OMS procedure under general anesthesia or sedationQuestionnaireQuestionnaire
Primary Outcome Measures
NameTimeMethod
Brice questionnaire at post-operative day 1post-operative day 1

The questionnaire attempts to identify patients who may have had memories of their operation i.e. accidental awareness under anesthesia. These are open questions.

Bauer questionnaire at post-operative day 1post-operative day 1

The Bauer questionnaire contains a set of questions on anaesthesia-related discomfort and another set on satisfaction with anaesthesia care in general. The questions on discomfort will be assessed on a 3-point scale, and those on patient satisfaction on a 4-point scale.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Ziekenhuis Oost-Limburg

🇧🇪

Genk, Belgium

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