Anesthesia ComplicationNCT03744455
Influence of Resident's Degree of Formation on the Quality of Care Delivered to the Patients.
An observational study of Anesthesia Complication, run by Astes at 1 site in Belgium.
Trial summary
The aim of this study is to evaluation the influence of the resident in anesthesiology's degree of formation on the quality of care delivered to the patient. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Anesthesia Complication
- What is being tested?
- Axillary Plexus
- How many people
- 188 participants
- Where
- 1 siteBelgium
- Study dates
- 1 Sep 2018to 1 Jan 2019
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Adult, Older adult
Study population: All patients scheduled for hand surgery under axillary plexus in the Clinique Saint-Luc of Bouge (Namur, Belgium)
Who may be able to join
- All patients scheduled for hand surgery under axillary plexus
Who cannot join
- Patient's refusal
Trial locations and contacts
1 site in 1 country.
About this study
The aim of this study is to evaluation the influence of the resident in anesthesiology's degree of formation on the quality of care delivered to the patient.
Read the detailed description
The aim of this study is to evaluation the influence of the resident in anesthesiology's degree of formation on the quality of care delivered to the patient.
To perform it, the investigators will enrolled all of the patients scheduled for an axillary plexus anesthesia technique in the Clinique Saint-Luc of Bouge in September 2018 (end of formation for the residents in anesthesia) and compare the patient's degree of satisfaction with the patients scheduled for the same kind of anesthesia on October and November 2018 (begin of formation for the residents in anesthesia).
- Conditions
- Anesthesia Complication
- Being tested
- Axillary Plexus
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Axillary PlexusBiological
Axillary plexus anesthesia technique for hand surgery
| Study group | Role | What they receive |
|---|---|---|
| End of training | Anesthesia residents at the end of their training who will realize axillary plexus. The satisfaction of the patient will be registered. Receives: Biological: Axillary Plexus | |
| Begin of training | Anesthesia residents at the begin of their training who will realize axillary plexus. The satisfaction of the patient will be registered. Receives: Biological: Axillary Plexus |
What is being measured
The primary outcome is the main question the study is designed to answer.
Patient satisfaction (Likert's scale)
Patient satisfaction after the completion of axillary plexus (satisfaction will be studied with a Lickert's scale). This scale will examine the patient's satisfaction in a scale ranging from 0 (worse satisfaction) to 5 (best satisfaction).
Measured: 1 day
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Nov 2018
- Study start1 Sep 2018
- Primary completion16 Nov 2018
- Study completion1 Jan 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Anesthesia ComplicationStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 188 participants (actual)
Sponsor and investigators
- Lead sponsor
- Astes
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Eric DEFLANDRE, MD, PhD, FCCP, FAHA, Astes
- Investigators
- Eric Deflandre, MD, PhD, Principal investigator, Astes
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03744455
- Sponsor's protocol ID
- PQR
- Status last verified
- Jan 2019
- First submitted
- 14 Nov 2018
- Last updated
- 10 Jan 2019
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 10 Jan 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Influence of Resident's Degree of Formation on the Quality of Care Delivered to the Patients.
- ClinicalTrials.gov ID
- NCT03744455
- Acronym / sponsor ID
- PQR
- Conditions
- Anesthesia Complication
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 188 participants (actual)
- Lead sponsor
- AstesUniversity, hospital or other
- Study start
- 1 Sep 2018 (actual)
- Primary completion
- 16 Nov 2018 (actual)
- Study completion
- 1 Jan 2019 (actual)
- First posted
- 16 Nov 2018 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The aim of this study is to evaluation the influence of the resident in anesthesiology's degree of formation on the quality of care delivered to the patient.
Detailed description
The aim of this study is to evaluation the influence of the resident in anesthesiology's degree of formation on the quality of care delivered to the patient.
To perform it, the investigators will enrolled all of the patients scheduled for an axillary plexus anesthesia technique in the Clinique Saint-Luc of Bouge in September 2018 (end of formation for the residents in anesthesia) and compare the patient's degree of satisfaction with the patients scheduled for the same kind of anesthesia on October and November 2018 (begin of formation for the residents in anesthesia).
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| End of training | – | Biological: Axillary PlexusAnesthesia residents at the end of their training who will realize axillary plexus. The satisfaction of the patient will be registered. |
| Begin of training | – | Biological: Axillary PlexusAnesthesia residents at the begin of their training who will realize axillary plexus. The satisfaction of the patient will be registered. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Age groups
- Adult, Older adult
- Study population
- All patients scheduled for hand surgery under axillary plexus in the Clinique Saint-Luc of Bouge (Namur, Belgium)
Key inclusion criteria (1 listed)
- All patients scheduled for hand surgery under axillary plexus
Key exclusion criteria (1 listed)
- Patient's refusal
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Axillary PlexusAxillary plexus anesthesia technique for hand surgery | Biological | Begin of training, End of training |
Primary outcome
Patient satisfaction (Likert's scale)
Time frame: 1 day
Patient satisfaction after the completion of axillary plexus (satisfaction will be studied with a Lickert's scale). This scale will examine the patient's satisfaction in a scale ranging from 0 (worse satisfaction) to 5 (best satisfaction).
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Jan 2019.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Eric Deflandre, MD, PhD principal investigator
Astes
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Anesthesia Complication, run by Astes at 1 site in Belgium.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 10 Jan 2019. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Belgium. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Patient satisfaction (Likert's scale) (time frame: 1 day). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Jan 2019.