- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05106621
AN INTELLIGENT MODEL FOR THE OPERATIVE BLOCK (BLOC-OP)
May 16, 2022 updated by: Elena Giovanna Bignami, University of Parma
NEW MODEL OF ORGANIZATION OF AN OPERATIVE BLOCK (BLOC-OP)
Perioperative medicine is characterized by a very delicate path; it is composed, in fact, of a series of highly specialized clinical measures managed by various professionals (surgeons, anesthetists, intensivists, nurses, etc.), who work together to ensure the best quality of all phases of the path (preoperative , intra and postoperative).
On the other hand, it is necessary to underline the huge resources needed to provide surgical services.
Organizational optimization, based on specific analyzes, could lead to a more careful management of resources in this area, avoiding waste due to early closure of the operating room or unexpected extension of the same.
In recent years, precisely to respond to the need to analyze large quantities of information, the use of artificial intelligence techniques, and in particular of machine learning, is becoming increasingly popular, a branch of artificial intelligence that aims, through the use of algorithms and statistical model, to infer new knowledge in a way automatic.
Such technologies appear to possess excellent analytical skills both in the clinical and, above all, organizational fields.
The data that are emerging in the literature on this issue, although still the first in this regard, seem to confirm this hypothesis.
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Anticipated)
142
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Elena Bignami
- Phone Number: 390521703567
- Email: elenagiovanna.bignami@unipr.it
Study Locations
-
-
-
Parma, Italy, 43125
- Recruiting
- Azienda Ospedaliera-Universitaria di Parma
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
all patients undergoing abdominal, thoracic, urological, vascular, orthopedic and gynecological and plastic surgery
Description
Inclusion Criteria:
all patients undergoing surgery who sign the informed consent form will be included.
Exclusion Criteria:
refusal of the patient to the study in question.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
Surgical Patients
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Surgical Time Prediction
Time Frame: 1 year
|
Prediction of time spend in oprating room
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Outcome evaluation
Time Frame: 1 year
|
ICU admission
|
1 year
|
Outcome evaluation
Time Frame: 1 year
|
Rate of surgical procedures cancellation
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Evans RS, Burke JP, Classen DC, Gardner RM, Menlove RL, Goodrich KM, Stevens LE, Pestotnik SL. Computerized identification of patients at high risk for hospital-acquired infection. Am J Infect Control. 1992 Feb;20(1):4-10. doi: 10.1016/s0196-6553(05)80117-8.
- Redfern RO, Langlotz CP, Abbuhl SB, Polansky M, Horii SC, Kundel HL. The effect of PACS on the time required for technologists to produce radiographic images in the emergency department radiology suite. J Digit Imaging. 2002 Sep;15(3):153-60. doi: 10.1007/s10278-002-0024-5. Epub 2002 Nov 6. Erratum In: J Digit Imaging. 2002 Sep;15(3):191.
- Lee TT, Liu CY, Kuo YH, Mills ME, Fong JG, Hung C. Application of data mining to the identification of critical factors in patient falls using a web-based reporting system. Int J Med Inform. 2011 Feb;80(2):141-50. doi: 10.1016/j.ijmedinf.2010.10.009. Epub 2010 Nov 5.
- Martins M. Use of comorbidity measures to predict the risk of death in Brazilian in-patients. Rev Saude Publica. 2010 Jun;44(3):448-56. doi: 10.1590/s0034-89102010005000003. Epub 2010 Apr 30.
- Izad Shenas SA, Raahemi B, Hossein Tekieh M, Kuziemsky C. Identifying high-cost patients using data mining techniques and a small set of non-trivial attributes. Comput Biol Med. 2014 Oct;53:9-18. doi: 10.1016/j.compbiomed.2014.07.005. Epub 2014 Jul 22.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
November 1, 2021
Primary Completion (ANTICIPATED)
November 30, 2022
Study Completion (ANTICIPATED)
November 30, 2022
Study Registration Dates
First Submitted
October 11, 2021
First Submitted That Met QC Criteria
October 22, 2021
First Posted (ACTUAL)
November 4, 2021
Study Record Updates
Last Update Posted (ACTUAL)
May 17, 2022
Last Update Submitted That Met QC Criteria
May 16, 2022
Last Verified
May 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- 1284/2020/OSS/AOUPR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.
Clinical Trials on Artificial Intelligence in Operating Room
-
Herlev HospitalCompletedSurgical Behaviour in the Operating RoomDenmark
-
Unity Health TorontoCompletedOperating Room EfficiencyCanada
-
Pusan National University Yangsan HospitalCompletedPatients Who Were Extubated in the Operating Room After Minimally Invasive Cardiac SurgeryKorea, Republic of
-
VA Office of Research and DevelopmentCompletedOperating Room SchedulingUnited States
-
Al Baraka Fertility HospitalAl-Azhar UniversityRecruitingARTIFICIAL INTELLIGENCE (AI) APPLICATIONS IN REPRODUCTIVE MEDICINEEgypt
-
xiaolong zhaoRecruitingArtificial Intelligence | Time in Range | Insulin TherapyChina
-
Cairo UniversityRecruiting
-
Istituto Clinico HumanitasCompletedArtificial IntelligenceItaly
-
Istituto Clinico HumanitasRecruitingArtificial IntelligenceItaly