- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04734119
Patient Satisfaction With Perioperative Anesthetic Care
Patient Satisfaction With Perioperative Anesthetic Care: Is Continuity of Care Crucial?
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Background: The doctor-patient relationship, medical competence and patient expectations influence patient satisfaction with anesthesia. Preoperatively all patients are routinely assessed by an anesthesiologist. However, in many centers, the anesthesiologist who performs the preoperative evaluation will not necessarily be the anesthesiologist who provides the intraoperative service. This study evaluated the effect of this practice on patient satisfaction, level of confidence and anxiety among adult patients undergoing elective surgery.
Methods: 100 patients scheduled for elective surgery under general anesthesia were randomly divided into 2 equal groups: In Group A patients were evaluated and anesthetized by the same anesthesiologist. In Group B the preoperative assessment and actual anesthesia was performed by two different anesthesiologists. On the first postoperative day all patients completed a questionnaire designed to evaluate their sense of preoperative security (confidence) and their overall satisfaction with the anesthetic experience.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Kfar Saba, Israel
- Meir medical center Kfar Saba
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients scheduled for elective surgery under general anesthesia
- Period- 12.2018-03.2019
- ASA score 1 to3
- Hebrew is the patient mother tongue
- The patient was pre-operatively evaluated by an anesthesiologist at least one day before surgery
- Duration of surgery is more than 1 hour
- The anesthesiologist has more than 2 years experience at work
Exclusion Criteria:
- The patient suffers from severe cognitive decline or severe psychiatric illness
- The patient is unable to answer the questionnaire by himself/herself
- The patient received pre-operative sedation
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Group A- same anesthesiologist
In Group A patients were evaluated preoperatively and anesthetized by the same anesthesiologist.
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Pre operative evaluation and anesthesia administration by the same anesthesiologist (instead of two different anesthesiologists, as routinely performed in our medical center)
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Group B- different anesthesiologist
In Group B the preoperative assessment and actual anesthesia was performed by two different anesthesiologists
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Level of patient satisfaction
Time Frame: Post operative day 1
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Level of patient satisfaction from anesthesia management, as described by patient questionnaire, ranked 1-5 (1- very satisfied, 5- not satisfied at all).
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Post operative day 1
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0226-18-MMC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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