Skip to main content
Clinical Trials/NCT02413775
NCT02413775
Completed
Not Applicable

Patient Survey as a Tool to Quality Assurance and Quality Improvement - Department of Anesthesiology and Operative Intensive Care (CCM/CVK), Charité - Universitätsmedizin Berlin

Charite University, Berlin, Germany1 site in 1 country821 target enrollmentApril 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Patient Satisfaction
Sponsor
Charite University, Berlin, Germany
Enrollment
821
Locations
1
Primary Endpoint
Patient satisfaction
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

One goal of the investigators of the Department of Anesthesiology and Operative Intensive Care Medicine CCM/CVK, Charité - Universitätsmedizin Berlin is a continuous improvement in the quality of care to the patients. One focus is the freezing preoperatively during surgery, and on the follow-up study to assess the perceived waiting times in the anesthesiology outpatient clinic.

The project aims to quality assurance and quality improvement of the Department of Anesthesiology and Operative Intensive Care Medicine CCM/CVK, Charité - Universitätsmedizin Berlin .

Detailed Description

The primary objective of the survey is to assess the entire perioperative care with particular focus on the development of perceived waiting times in the anesthesiology outpatient clinic, re-evaluation of the preoperative freezing the preoperative thirst, pain, nausea and vomiting after surgery (PONV prophylaxis). The survey will be repeated in a three-year interval (approximately 1000 - 2000 patients per survey) to monitor and improve the quality of the Department of Anesthesiology and Operative Intensive Care Medicine CCM/CVK, Charité - Universitätsmedizin Berlin from the patient point of view. In order to achieve a meaningful data collection, a response rate of 50 percent should be achieved.

Registry
clinicaltrials.gov
Start Date
April 2015
End Date
September 2021
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Claudia Spies

Clinic Director of the Department of Anesthesiology and Operative Intensive Care Medicine, CCM/CVK

Charite University, Berlin, Germany

Eligibility Criteria

Inclusion Criteria

  • male and female patients who underwent a procedure in anesthesia and willing to take part in the Survey
  • aged \>= 1 years

Exclusion Criteria

  • unconscious patients,
  • refusal by patient / parents

Outcomes

Primary Outcomes

Patient satisfaction

Time Frame: Time during hospital stay, an average of 2 weeks

Patient satisfaction with the care provided by the staff of the Department of Operative Anesthesiology and Intensive Care Medicine CCM/CVK; Measurement of satisfaction: Yes/No/Partly

Secondary Outcomes

  • Fear reduction during the premedication visit(Time in the outpatient clinic of anesthesia, an average of 1 hour)
  • Information provided during the premedication visit by educational films(Time in the outpatient clinic of anesthesia, an average of 1 hour)
  • Friendliness of staff(Time in the intensive care unit or post anesthesia care unit, an average of 3 days)
  • Sufficient pain treatment(Time in the operation room before start of anesthesia, an average of 30 minutes)
  • Post-operative nausea and vomiting (PONV)(Time during hospital stay, an average of 2 weeks)
  • Atmosphere(Time in the intensive care unit or post anesthesia care unit, an average of 3 days)
  • Choosing of Patient controlled anesthesia(Time during hospital stay, an average of 2 weeks)
  • Compliance with the planned start of the operation(Time in the operation room before start of anesthesia, an average of 30 minutes)
  • Thirst(Time in the operation room before start of anesthesia, an average of 30 minutes)
  • Sufficient therapy in case of PONV(Time in the intensive care unit or post anesthesia care unit, an average of 3 days)
  • Sufficient therapy in case of pain(Time during hospital stay, an average of 2 weeks)
  • Postoperative patient controlled analgesia(Time during hospital stay, an average of 2 weeks)
  • Information provided during the premedication visit by the anesthetist(Time in the outpatient clinic of anesthesia, an average of 1 hour)
  • Response to questions during the premedication visit(Time in the outpatient clinic of anesthesia, an average of 1 hour)
  • Fear(Time in the operation room before start of anesthesia, an average of 30 minutes)
  • Pain(Time in the operation room before start of anesthesia, an average of 30 minutes)
  • Regional anaesthesia(Time during hospital stay, an average of 2 weeks)
  • In case of need choosing of regional anaesthesia again(Time during hospital stay, an average of 2 weeks)
  • Satisfaction of care through pain service(Time during hospital stay, an average of 2 weeks)
  • Postoperative fear(Time in the intensive care unit or post anesthesia care unit, an average of 3 days)
  • Waiting time in the premedication visit(Time in the outpatient clinic of anesthesia, an average of 1 hour)
  • Sufficient therapy in case of shivering(Time in the intensive care unit or post anesthesia care unit, an average of 3 days)
  • Pain intensity(Time in the intensive care unit or post anesthesia care unit, an average of 3 days)
  • Postoperative pain(Time during hospital stay, an average of 2 weeks)
  • Friendliness of the staff during the premedication visit(Time in the outpatient clinic of anesthesia, an average of 1 hour)
  • Shivering(Time in the intensive care unit or post anesthesia care unit, an average of 3 days)
  • Satisfaction with regional anaesthesia(Time during hospital stay, an average of 2 weeks)
  • Recommendation of medical care (provided by the staff from the Department of Anesthesiology and Intensive Care CVK/CCM)(Time during hospital stay, an average of 2 weeks)

Study Sites (1)

Loading locations...

Similar Trials