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Intelligent Operating Room (InOR) for Orthopaedic Surgery

Intelligent Operating Room (InOR) for Orthopaedic Surgery

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04167787
Acronym
InOR
Enrollment
150
Registered
2019-11-19
Start date
2019-10-10
Completion date
2020-12-02
Last updated
2019-11-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee Replacement, Musculoskeletal

Keywords

Surgery

Brief summary

The objective of the study is to evaluate the usefulness of digital technologies to support surgical teams before, during, and after an operation.

Interventions

None listed

Sponsors

University College London Hospitals
CollaboratorOTHER
Digital Surgery Ltd.
Lead SponsorINDUSTRY

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Inclusion Criteria: * Adult patients 18-99 years. * All willing patients undergoing elective total and unicondylar knee replacement (both navigated and robotic-assisted). *

Exclusion criteria

* Patients/staff who are unwilling to participate in the study * Patients/staff that withdraw from the study * Two stage revisions for infected primary total knee replacements, multiple stage procedures for complex deformities, * Single stage revision procedures with the need for special instruments and modified steps * Patients with cognitive impairment/ special cognitive needs. * \<18 years old

Design outcomes

Primary

MeasureTime frameDescription
Change in baseline scores of qualitative questionnaires (every 8 weeks in one surgical team).14 monthsTo determine how digital technologies and advanced data analytics can improve team coordination, efficiency and performance intraoperatively through understanding and mapping of surgical workflows and instrumentation use.

Secondary

MeasureTime frameDescription
Report the effect of presenting information intraoperatively through digital displays and augmented reality headsets.14 monthsAssessed through monitoring scores from qualitative questionnaires of the surgical team;
To provide automatic post-operative analytics after each surgical operation (up to 150 cases).14 monthsIncluding phase timings and instrumentation

Countries

United Kingdom

Contacts

Primary ContactKaren Kerr, Dr
karen.kerr@touchsurgery.com07967135052

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026