CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 243 enrolled
Drug / intervention
Surgical simulation training in primary Total Hip Arthroplasty +2 morebehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04267172
NCT04267172N/ACompleted

A Prospective Randomised Controlled Study Assessing the Impact of Simulation Training in Primary Total Hip Replacement (THR).

University of Oxford·interventional·Posted Feb 12, 2020·Updated Jan 3, 2025

In Brief

A clinical study evaluating Surgical simulation training in primary Total Hip Arthroplasty, No intervention: Surgical Resident Control Group, and 1 other intervention for Hip Osteoarthritis. Completed, enrolled 243 participants across 1 site.

Detailed Summary

This research study is focused upon assessing and optimising surgeon's performance during, and patient outcomes following, primary total hip replacement (THR) surgery. The primary research question is to determine if additional simulation training can improve the intra-operative performance of surgical trainees (Residents) during a THR, or the outcome of patients after their THR. The investigators will aim to define an 'expert' standard in performing a primary elective THR, which may be used as a benchmark when assessing surgical trainee performance; and also determine if operative surgeon performance metrics during a THR are correlated with surgical experience, or patient outcomes.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited Kingdom

Timeline

N/ACompletedFinished
2020202120222023202420252026
First PostedFeb 12, 2020
Enrollment StartFeb 26, 2020
Primary CompletionFeb 28, 2022
TodayJul 2, 2026
Enrollment to primary: 2.0 yearsPosted 6.4 years ago

Interventions

Surgical simulation training in primary Total Hip Arthroplastybehavioral

The simulation-based and cognitive learning package will be delivered to a randomised sub-group of 50% of the Surgical Residents recruited into this study. This will be delivered in a supervised non-clinical setting within a dedicated University-owned simulation laboratory over a 4-week period for between 1 to 2 hours per week, over 3 to 4 consecutive but separate six-month placements.

No intervention: Surgical Resident Control Groupother

Control Group

No Intervention: Consultant and Fellow Comparator Groupother

Comparator Group