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Development and Validation of Precise Preoperative Equipping Strategies for Loaded Medical Instruments in Total Knee Arthroplasty

Development and Validation of Precise Preoperative Equipping Strategies for Loaded Medical Instruments in Total Knee Arthroplasty

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095756
Enrollment
Unknown
Registered
2025-01-13
Start date
2025-01-20
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Total Knee Arthroplasty

Interventions

experimental group:A strategy of precise preoperative preparation of loaded medical instruments for total knee arthroplasty is adopted for preoperative equipment preparation of total knee arthroplasty
Historical control group 1:From June 1, 2023 to June 30, 2024, traditional loaded instrument management methods was used to configure instruments for total knee arthroplasty
Historical control group 2:From June 1, 2023 to June 30, 2024, a multidisciplinary collaborative approach was adopted to manage loaded instruments for total knee arthroplasty

Sponsors

Beijing Jishuitan Hospital Guizhou Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
22 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Research object 1: Focus discussion group members Inclusion criteria: ? Ability to independently complete surgical cooperation; ? Informed and voluntary participation in this study. (2) Research object 2: Operating room nurses participating in total knee arthroplasty The inclusion criteria are informed consent and voluntary participation in this study. (3) Research object 3: Loaded medical instruments used for total knee arthroplasty Inclusion criteria: Loaded medical instruments used by patients undergoing total knee arthroplasty for the first time. (4) Research object 4: Professional personnel related to operating room nursing The inclusion criteria are informed and voluntary participation in this study.

Exclusion criteria

Exclusion criteria: (1) Research object 1: Focus discussion group members Exclusion criteria: ? Personnel who study or take leave outside; ? Withdraw from this study midway. (2) Research object 2: Operating room nurses participating in total knee arthroplasty Exclusion criteria: ? Nurses who go out for study or vacation; ? Withdraw from this study midway. (3) Research object 3: Loaded medical instruments used for total knee arthroplasty Exclusion criteria: Defective and incompatible instruments. (4) Research object 4: Professional personnel related to operating room nursing The exclusion criteria are those who withdraw from the study midway.

Design outcomes

Primary

MeasureTime frame
Duration of standard placement of loaded medical instruments;Qualified rate of standard placement of loaded medical instruments;Duration of inventory and consumption of loaded medical instruments;Occurrence rate of errors in re-counting of loaded medical instruments;

Secondary

MeasureTime frame
The quantity of foreign medical device packages used;Surgical doctor satisfaction;

Countries

China

Contacts

Public ContactJing Wang

Beijing Jishuitan Hospital Guizhou Hospital

13984356767@163.com+86 177 8515 9107

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026