Resident EducationPROMOTENCT05887570
Procedure-Specific Resident Objective Modular Training Evaluation
A study testing Educational intervention in people with Resident Education, run by University of British Columbia at 1 site in Canada.
Trial summary
Funding for resident training is continually decreasing. The investigators hope to look at innovative ways to improve resident education. The project will investigate whether skills acquired in a surgical lab result in improved operating room (OR) surgical skills. Read more about this study
- Who is it for?
- Ages 19 years and older
- Conditions the study is for
- Resident Education
- What is being tested?
- Educational intervention
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 83 participants
- Where
- 1 siteCanada
- Study dates
- 13 Jun 2011to 2 Jul 2024
- Phase
- Interventional
- 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 19 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- An Obstetrics and Gynaecology residents/medical students/ fellow/junior staff in the UBC program General surgery residents Willing to participate Previous performance of less than 5 of each of the index procedures independently in the OR
Who cannot join
- Previous performance of 5 or more of each of the index procedures independently in the OR
- For the cutoff score participants there is no exclusion criteria.
Trial locations and contacts
1 site in 1 country.
About this study
Funding for resident training is continually decreasing. The investigators hope to look at innovative ways to improve resident education. The project will investigate whether skills acquired in a surgical lab result in improved operating room (OR) surgical skills. This will be a randomized controlled trial that will split residents up into an intervention group and a control group. The intervention group will be required to pass training modules for six essential surgeries before operating in the OR. In the OR, both groups will be graded by the supervising doctor and be asked to rate themselves using validated questionnaires.
Read the detailed description
- Purpose: The purpose is to investigate whether procedure-specific skills acquired in a surgical lab result in improved OR surgical skills; to examine related outcomes of intra-operative events and resident satisfaction; to examine the feasibility of implementation of modular training in a gynecology residency program.
- Hypothesis: That the surgical training modules proposed will improve resident surgical skills in the operating room.
- Justification: Increasing constraints are placed on the educational experience of young surgical trainees. Specifically in the area of Obstetrics and Gynecology (ObGyn), residents are expected to become skilled surgeons in addition to acquiring vast knowledge on a myriad of women's health topics. Operating room (OR) time is scarce. Medicolegal concerns can be a limitation to resident involvement. Financial incentives to support surgical mentorship are dwindling. With the rapid acceptance and advancement of minimally invasive surgical techniques in gynecology, there is a learning curve for the attending surgeons who must familiarize themselves with the techniques first and thus give fewer practice opportunities to residents. Traditionally, acquisition of surgical technical skills happens through repetition in the OR, under the supervision of an experienced surgeon. Because of the above named constraints, surgical education of residents has been referred to as "education by random opportunity". Surgical educators have thus attempted to teach in other settings, remote from the OR. Options have included the use of suturing stations, animal and cadaver models, videotapes of procedures and laparoscopic simulators. Although the efficacy of these options is recognized, few ObGyn programs provide formal surgical curricula and technical skills are still taught mostly in the OR and through lectures. A survey of all the 266 ObGyn residency programs in the United States, published more than 10 years ago, showed that surgical teaching curricula were only used by 29% of the programs. A more recent survey conducted in Canada showed that, 10 years later, only 40% of Canadian ObGyn programs compared to 76% of other surgical residencies used a program-specific surgical training curriculum. Most Canadian residency program directors who did not have access to a standard training curriculum wished to have one implemented. Results of this survey are consistent with other Canadian studies showing variability in training and assessment of surgical skill across Canada. Without a formal curriculum, residents may graduate with widely varying surgical skills, currently not objectively evaluated as a requirement for graduation. There are obvious advantages to a surgical training curriculum remote from the OR. Residents can practice basic and advanced skills as many times as necessary to achieve competency prior to performing surgeries on real patients. Patient safety is thus not compromised. Dedicated teaching faculty can provide immediate feedback. If training objectives are not met, mandatory retraining targeted to specific deficient areas can be undertaken on the same modules. Many tools are available for designing an appropriate specialty-specific curriculum. A review of these tools concluded that based on the available evidence a successful curriculum would include didactic training and surgical anatomy, the practice of surgical skills on box trainers and animal models followed by consolidation of skills in the real OR). A Canadian curriculum with surgical training in various core surgical skills did not result in improvement in performance of actual surgical procedures on a cadaver assessment model. On the other hand, a laparoscopic training module in basic laparoscopic tasks has been shown to impart skills transferable to real OR General Surgery procedures. In ObGyn, transferability of skills to the OR has been demonstrated after instruction via procedure-specific modules for laparoscopic tubal ligation and episiotomy repair. Our primary aim in the current study is to investigate whether instruction via procedure-specific surgical modules results in transferability of resident surgical skill to real OR urogynecologic procedures. Secondary aims include impact of this instruction on patient outcomes, resident case volume, need for remedial instruction, cost and feasibility as well as resident satisfaction and self-confidence. Our ultimate long-term goal is to disseminate our findings across Canada and hopefully encourage all ObGyn programs to adopt an evidence-based, competency-based, modular, standard training approach to training gynecologic surgeons.
- Objectives: Primary: To investigate whether procedure-specific skills acquired in a surgical lab result in improved OR surgical skills as tested via a global rating scale on each of several index procedures. Secondary:
- To investigate whether procedure-specific skills acquired in a surgical lab result in improved knowledge of procedural steps on each of several index procedures
- To investigate whether procedure-specific skills acquired in a surgical lab result in less OR time, fewer intraoperative complications and less blood loss on each of several index procedures
- To examine how the implementation of modular training affects resident case volume in the first two months after implementation.
- To determine the proportion of residents needing remedial training after module completion and examine the feasibility of retraining given constraints of time and cost
- To examine the cost of implementation of modular training in urogynecology procedures in a gynecology residency program.
- To examine resident satisfaction and self-confidence with operative skills after modular training
- Research Method: Design This study is a randomized controlled trial of an intervention group, consisting of surgical training in specific urogynecologic procedures via modules versus a control group, consisting of usual training. Thirty ObGyn junior residents having performed less than five of each index procedure independently will be recruited to participate. Baseline demographics and number of index procedures performed independently prior to enrollment will be recorded. A baseline knowledge pretest consisting of multiple choice and short answer questions on technical aspects of the index procedures will be administered to all residents. The residents in the intervention group will then receive individual training. Each index procedure will be taught using a module. Each procedure-specific module consists of a didactic component, practice on suturing, knot tying and technical aspects of the procedure with individual feedback, and evaluation. Evaluation consists of a knowledge posttest and a practical examination of acquired surgical skills on procedure-specif practical models. If the resident fails the written or practical examinations, he/she will not be allowed to perform surgery in the real OR but will undergo mandatory retraining using the same modules. When considered competent by passing the written and practical examinations, the resident will then be allowed to independently perform corresponding index procedures in the real OR and will be evaluated via a validated global rating scale of surgical skill. The residents in the control group will undergo training as usual by individual reading and observation and practice in the OR. When allowed to independently perform one of the index procedures, their performance will be evaluated via a validated global rating scale of surgical skill. After the data collection is complete on the last index procedure, residents in the control group will be offered the same surgical training given to the residents in the intervention group. This will be done to ensure equal training opportunities for all residents. Sample Size: We used the GRS developed by Reznick et al11 and previously used to compare gynaecology residents trained on an episiotomy repair module versus controls. Banks et al established a 21% significant difference in scores for the episiotomy repair module versus controls.17 As our index procedures are more advanced then episiotomy repair, we determined that 50 residents (25 per group) were required to find a 20 point overall difference (out of 100) in mean global rating scale (GRS) score between intervention and control residents, with a standard deviation of 25 points (to account for the variation in surgical skill of residents), 80% power and a significance level of 0.05.
- Statistical Analysis:
Statistical analysis
- Primary outcome: Student's t-test for Global Rating Scale score average on each index procedure in the OR - intervention residents versus controls
- Secondary outcomes: Student's t-test for procedural steps scale score average - intervention residents versus controls; Mann-Whitney test for average OR time (expressed in minutes) and estimated blood loss (expressed in milliliters) - intervention residents versus controls (results likely not normally distributed); descriptive statistics for intraoperative complications - intervention residents versus controls; student's t-test for number of cases performed in the OR in the 2 months following intervention - intervention residents versus controls; proportion of intervention residents requiring remedial training and cost thereof; cost of implementation of modular training; student's t-test for Self Confidence Scale score average and satisfaction score average on each index procedure in the OR - intervention residents versus controls; chi square test for differences in outcomes based on categorical variables of year of training and number of previously performed index procedures
- Conditions
- Resident Education
- Being tested
- Educational intervention, Control - Regular Instruction
- Keywords
- education
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Educational interventionBehavioural
intervention through extra education, modules, instruction on models
Control - Regular InstructionOther
participants receive usual training
| Study group | Role | What they receive |
|---|---|---|
| Intervention | Experimental | Specific intervention:
Modules for each of the above comprising:
1. didactic lecture on indications and contraindications of procedure, surgical anatomy, patient positioning in the OR, anesthesia type, suture materials and suturing techniques;
2. practical component with hands-on surgical skill training in basic and advanced techniques relevant to each procedure
3. immediate feedback from dedicated educator on technical aspects
4. post-test Receives: Behavioral: Educational intervention |
| Control - | Placebo comparator | This group receives regular instruction. Receives: Other: Control - Regular Instruction |
What is being measured
The primary outcome is the main question the study is designed to answer.
Primary Outcome - investigation of whether procedure-specific skills acquired in surgical lab
To investigate whether procedure-specific skills acquired in a surgical lab result in improved OR surgical skills as tested via a global rating scale on each of several index procedures.
Measured: through study completion, on average 1 year
Secondary outcomes (5)
Secondary Outcome 1 - Improved Knowledge
To investigate whether procedure-specific skills acquired in a surgical lab result in improved knowledge of procedural steps on each index procedures using a global rating scale
Measured: through study completion, on average 1 year
Secondary Outcome 2 - Less OR Time
Procedure-specific skills acquired in a surgical lab may result in less OR time will be determined through the recording of intra operative time/complications between the two groups
Measured: through study completion, on average 1 year
Secondary Outcome 3 - Implemention of modular training
To examine how the implementation of modular training affects resident case volume in the first two months after implementation.
Measured: through study completion, on average 1 year
Seconday Outcome 4 - remedial training
To determine the proportion of residents needing remedial training after module completion and examine the feasibility of retraining given constraints of time and cost
Measured: through study completion, on average 1 year
Secondary Outcome 6 - Resident satisfaction and self confidence
-To examine resident satisfaction and self-confidence with operative skills after modular training using a resident self satifisfaction scale/resident confidence scale
Measured: through study completion, on average 1 year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Jun 2023
- Study start13 Jun 2011
- Primary completion2 Jul 2024
- Study completion2 Jul 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Resident EducationStudies of the same condition, open and under way.
- More trials run by University of British ColumbiaThe sponsor's other registered studies.
- 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Single group
- Model description
- Educational Intervention
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 83 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of British Columbia
- Sponsor type
- University, hospital or other
- Collaborators
- Royal College of Physicians and Surgeons of Canada, University of Calgary, University of Alberta
- Responsible party
- Principal investigator, Roxana Geoffrion, University of British Columbia
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05887570
- Sponsor's protocol ID
- H11-00779
- Acronym
- PROMOTE
- Status last verified
- Oct 2024
- First submitted
- 4 May 2023
- Last updated
- 18 Oct 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Geoffrion R, Koenig NA, Cundiff GW, Flood C, Hyakutake MT, Schulz J, Brennand EA, Lee T, Singer J, Todd NJ. Procedure-specific simulation for vaginal surgery training: A randomized controlled trial. Acta Obstet Gynecol Scand. 2024 Jun;103(6):1165-1174. doi: 10.1111/aogs.14810. Epub 2024 Feb 21.
PubMed 38382912
Study at a glance
From the registry record, last updated by the sponsor on 18 Oct 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Procedure-Specific Resident Objective Modular Training Evaluation
- ClinicalTrials.gov ID
- NCT05887570
- Acronym / sponsor ID
- PROMOTE / H11-00779
- Conditions
- Resident Education
- Keywords
- education
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 83 participants (actual)
- Lead sponsor
- University of British ColumbiaUniversity, hospital or other
- Collaborators
- Royal College of Physicians and Surgeons of Canada, University of Calgary, University of Alberta
- Study start
- 13 Jun 2011 (actual)
- Primary completion
- 2 Jul 2024 (actual)
- Study completion
- 2 Jul 2024 (actual)
- First posted
- 2 Jun 2023 (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.
Funding for resident training is continually decreasing. The investigators hope to look at innovative ways to improve resident education. The project will investigate whether skills acquired in a surgical lab result in improved operating room (OR) surgical skills. This will be a randomized controlled trial that will split residents up into an intervention group and a control group. The intervention group will be required to pass training modules for six essential surgeries before operating in the OR. In the OR, both groups will be graded by the supervising doctor and be asked to rate themselves using validated questionnaires.
Detailed description
- Purpose: The purpose is to investigate whether procedure-specific skills acquired in a surgical lab result in improved OR surgical skills; to examine related outcomes of intra-operative events and resident satisfaction; to examine the feasibility of implementation of modular training in a gynecology residency program.
- Hypothesis: That the surgical training modules proposed will improve resident surgical skills in the operating room.
- Justification: Increasing constraints are placed on the educational experience of young surgical trainees. Specifically in the area of Obstetrics and Gynecology (ObGyn), residents are expected to become skilled surgeons in addition to acquiring vast knowledge on a myriad of women's health topics. Operating room (OR) time is scarce. Medicolegal concerns can be a limitation to resident involvement. Financial incentives to support surgical mentorship are dwindling. With the rapid acceptance and advancement of minimally invasive surgical techniques in gynecology, there is a learning curve for the attending surgeons who must familiarize themselves with the techniques first and thus give fewer practice opportunities to residents. Traditionally, acquisition of surgical technical skills happens through repetition in the OR, under the supervision of an experienced surgeon. Because of the above named constraints, surgical education of residents has been referred to as "education by random opportunity". Surgical educators have thus attempted to teach in other settings, remote from the OR. Options have included the use of suturing stations, animal and cadaver models, videotapes of procedures and laparoscopic simulators. Although the efficacy of these options is recognized, few ObGyn programs provide formal surgical curricula and technical skills are still taught mostly in the OR and through lectures. A survey of all the 266 ObGyn residency programs in the United States, published more than 10 years ago, showed that surgical teaching curricula were only used by 29% of the programs. A more recent survey conducted in Canada showed that, 10 years later, only 40% of Canadian ObGyn programs compared to 76% of other surgical residencies used a program-specific surgical training curriculum. Most Canadian residency program directors who did not have access to a standard training curriculum wished to have one implemented. Results of this survey are consistent with other Canadian studies showing variability in training and assessment of surgical skill across Canada. Without a formal curriculum, residents may graduate with widely varying surgical skills, currently not objectively evaluated as a requirement for graduation. There are obvious advantages to a surgical training curriculum remote from the OR. Residents can practice basic and advanced skills as many times as necessary to achieve competency prior to performing surgeries on real patients. Patient safety is thus not compromised. Dedicated teaching faculty can provide immediate feedback. If training objectives are not met, mandatory retraining targeted to specific deficient areas can be undertaken on the same modules. Many tools are available for designing an appropriate specialty-specific curriculum. A review of these tools concluded that based on the available evidence a successful curriculum would include didactic training and surgical anatomy, the practice of surgical skills on box trainers and animal models followed by consolidation of skills in the real OR). A Canadian curriculum with surgical training in various core surgical skills did not result in improvement in performance of actual surgical procedures on a cadaver assessment model. On the other hand, a laparoscopic training module in basic laparoscopic tasks has been shown to impart skills transferable to real OR General Surgery procedures. In ObGyn, transferability of skills to the OR has been demonstrated after instruction via procedure-specific modules for laparoscopic tubal ligation and episiotomy repair. Our primary aim in the current study is to investigate whether instruction via procedure-specific surgical modules results in transferability of resident surgical skill to real OR urogynecologic procedures. Secondary aims include impact of this instruction on patient outcomes, resident case volume, need for remedial instruction, cost and feasibility as well as resident satisfaction and self-confidence. Our ultimate long-term goal is to disseminate our findings across Canada and hopefully encourage all ObGyn programs to adopt an evidence-based, competency-based, modular, standard training approach to training gynecologic surgeons.
- Objectives: Primary: To investigate whether procedure-specific skills acquired in a surgical lab result in improved OR surgical skills as tested via a global rating scale on each of several index procedures. Secondary:
- To investigate whether procedure-specific skills acquired in a surgical lab result in improved knowledge of procedural steps on each of several index procedures
- To investigate whether procedure-specific skills acquired in a surgical lab result in less OR time, fewer intraoperative complications and less blood loss on each of several index procedures
- To examine how the implementation of modular training affects resident case volume in the first two months after implementation.
- To determine the proportion of residents needing remedial training after module completion and examine the feasibility of retraining given constraints of time and cost
- To examine the cost of implementation of modular training in urogynecology procedures in a gynecology residency program.
- To examine resident satisfaction and self-confidence with operative skills after modular training
- Research Method: Design This study is a randomized controlled trial of an intervention group, consisting of surgical training in specific urogynecologic procedures via modules versus a control group, consisting of usual training. Thirty ObGyn junior residents having performed less than five of each index procedure independently will be recruited to participate. Baseline demographics and number of index procedures performed independently prior to enrollment will be recorded. A baseline knowledge pretest consisting of multiple choice and short answer questions on technical aspects of the index procedures will be administered to all residents. The residents in the intervention group will then receive individual training. Each index procedure will be taught using a module. Each procedure-specific module consists of a didactic component, practice on suturing, knot tying and technical aspects of the procedure with individual feedback, and evaluation. Evaluation consists of a knowledge posttest and a practical examination of acquired surgical skills on procedure-specif practical models. If the resident fails the written or practical examinations, he/she will not be allowed to perform surgery in the real OR but will undergo mandatory retraining using the same modules. When considered competent by passing the written and practical examinations, the resident will then be allowed to independently perform corresponding index procedures in the real OR and will be evaluated via a validated global rating scale of surgical skill. The residents in the control group will undergo training as usual by individual reading and observation and practice in the OR. When allowed to independently perform one of the index procedures, their performance will be evaluated via a validated global rating scale of surgical skill. After the data collection is complete on the last index procedure, residents in the control group will be offered the same surgical training given to the residents in the intervention group. This will be done to ensure equal training opportunities for all residents. Sample Size: We used the GRS developed by Reznick et al11 and previously used to compare gynaecology residents trained on an episiotomy repair module versus controls. Banks et al established a 21% significant difference in scores for the episiotomy repair module versus controls.17 As our index procedures are more advanced then episiotomy repair, we determined that 50 residents (25 per group) were required to find a 20 point overall difference (out of 100) in mean global rating scale (GRS) score between intervention and control residents, with a standard deviation of 25 points (to account for the variation in surgical skill of residents), 80% power and a significance level of 0.05.
- Statistical Analysis:
Statistical analysis
- Primary outcome: Student's t-test for Global Rating Scale score average on each index procedure in the OR - intervention residents versus controls
- Secondary outcomes: Student's t-test for procedural steps scale score average - intervention residents versus controls; Mann-Whitney test for average OR time (expressed in minutes) and estimated blood loss (expressed in milliliters) - intervention residents versus controls (results likely not normally distributed); descriptive statistics for intraoperative complications - intervention residents versus controls; student's t-test for number of cases performed in the OR in the 2 months following intervention - intervention residents versus controls; proportion of intervention residents requiring remedial training and cost thereof; cost of implementation of modular training; student's t-test for Self Confidence Scale score average and satisfaction score average on each index procedure in the OR - intervention residents versus controls; chi square test for differences in outcomes based on categorical variables of year of training and number of previously performed index procedures
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Single group
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
- Model description
- Educational Intervention
| Arm | Type | Receives |
|---|---|---|
| Intervention | Experimental | Behavioral: Educational interventionSpecific intervention: Modules for each of the above comprising: 1. didactic lecture on indications and contraindications of procedure, surgical anatomy, patient positioning in the OR, anesthesia type, suture materials and suturing techniques; 2. practical component with hands-on surgical skill training in basic and advanced techniques relevant to each procedure 3. immediate feedback from dedicated educator on technical aspects 4. post-test |
| Control - | Placebo comparator | Other: Control - Regular InstructionThis group receives regular instruction. |
Who may qualify
- Ages
- 19 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- An Obstetrics and Gynaecology residents/medical students/ fellow/junior staff in the UBC program General surgery residents Willing to participate Previous performance of less than 5 of each of the index procedures independently in the OR
Key exclusion criteria (2 listed)
- Previous performance of 5 or more of each of the index procedures independently in the OR
- For the cutoff score participants there is no exclusion criteria.
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 |
|---|---|---|
| Educational interventionintervention through extra education, modules, instruction on models | Behavioural | Intervention |
| Control - Regular Instructionparticipants receive usual training | Other | Control - |
Primary outcome
Primary Outcome - investigation of whether procedure-specific skills acquired in surgical lab
Time frame: through study completion, on average 1 year
To investigate whether procedure-specific skills acquired in a surgical lab result in improved OR surgical skills as tested via a global rating scale on each of several index procedures.
5 secondary outcomes
Secondary Outcome 1 - Improved Knowledge
Time frame: through study completion, on average 1 year
Secondary Outcome 2 - Less OR Time
Time frame: through study completion, on average 1 year
Secondary Outcome 3 - Implemention of modular training
Time frame: through study completion, on average 1 year
Seconday Outcome 4 - remedial training
Time frame: through study completion, on average 1 year
Secondary Outcome 6 - Resident satisfaction and self confidence
Time frame: through study completion, on average 1 year
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 18 Oct 2024.
- Derived from this study: PubMed 38382912Geoffrion R, Koenig NA, Cundiff GW, Flood C, Hyakutake MT, Schulz J, Brennand EA, Lee T, Singer J, Todd NJ. Procedure-specific simulation for vaginal surgery training: A randomized controlled trial. Acta Obstet Gynecol Scand. 2024 Jun;103(6):1165-1174. doi: 10.1111/aogs.14810. Epub 2024 Feb 21.
- Individual participant dataSharing planned: No
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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.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Educational intervention in people with Resident Education, run by University of British Columbia at 1 site in Canada.
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 2 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 18 Oct 2024. 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 Canada. 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. Some participants in this study may receive a placebo. 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?
Primary Outcome - investigation of whether procedure-specific skills acquired in surgical lab (time frame: through study completion, on average 1 year). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05887570, which also lists 1 linked publication.
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 18 Oct 2024; AzTrials last refreshed its copy on 27 Oct 2026.