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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03869996
Other study ID # 0001094
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 25, 2019
Est. completion date November 1, 2025

Study information

Verified date October 2023
Source Istituto Ortopedico Rizzoli
Contact Martina Rocchi, MD
Phone 00393338705057
Email martina.rocchi@ior.it
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Fast-track total knee arthroplasty (TKA) is a well-established concept including optimized logistics and evidence-based treatment, focusing on minimizing surgical stress and improved post-operative recovery. The aim of this protocol is to compare the standard care and fast track total knee arthroplasties in terms of functional and subjective outcomes, hospital staying, number of transfusions and analgesic consumption.


Description:

The aim of this protocol is to compare standard care and fast track total knee arthroplasties. The fast track care consists of: - preoperative educational lesson in which orthopedic surgeon, anesthesiologist and physiotherapist illustrate the operative and post operative path to the patients - antalgic protocol administered only orally - early rehabilitation care. The day of the surgical operation, the physiotherapist helps the patient reach the upright position. The standard care consists of usual antalgic and physiotherapy post-operative care: - Antalgic protocol consist in intravenous drugs - the first physiotherapy session is the day after surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 64
Est. completion date November 1, 2025
Est. primary completion date October 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 78 Years
Eligibility Inclusion Criteria: - patients affected by knee osteoarthritis, eligible for primary total knee arthroplasty - BMI < 32 - Time up ang go test </= 12 seconds - American Society of Anesthesiologists physical status classification system (ASA) </= 2 - preoperative hemoglobin (HB) >13 g/dl - patients eligible for spinal anesthesia - presence of a care-giver Exclusion Criteria: - psychiatric diseases - preoperative use of crutches - ASA > 3 - preoperative HB < 13 g/dl

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
fast track care protocol
fast track care consists in educational preoperative preparation for patients, particular strategies for controlling pain and bleeding and intensive early rehabilitation protocol.
standard care protocol
standard care protocol consists in the same surgical intervention without educational preoperative preparation for patients and intensive early rehabilitation protocol.

Locations

Country Name City State
Italy Istituto Ortopedico Rizzli Bologna

Sponsors (1)

Lead Sponsor Collaborator
Istituto Ortopedico Rizzoli

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Early functional outcomes Early functional outcomes are collecting using Lowa Level of Assistance(ILOA) during the third post-operative day. This scale is able to provide data on the autonomy reached by the patient in the first postoperative period going to investigate five main motor activities (get up from supine to seated, from sitting to standing position, walk around, take three steps, the speed of walking). the total score can vary from 0 to 50, where 50 indicates better functional results. Third post operative day
Secondary hospital staying The collection of hospital stay for each patient. The fast track expecting hospital stay is three days. Third day after surgery
Secondary Incidence of early major complications The collection of acute infection and early fracture Third day after surgery
Secondary Number of transfusions the collection of number of transfusions during hospital staying Third day after surgery
Secondary Analgesic consumption The request for analgesic rescue in relation to fast track standard analgesic scheme Third day after surgery
Secondary Knee Society Score (KSS) at 6 weeks The collection of functional outcomes score KSS at 6 weeks. The Knee Society Score (KSS) is mixed outcome measure that's both objective (physician input) and subjective (patient input). A score between 80 and 100 is considered excellent, between 70 and 79 is considered good, between 60 and 69 is considered fair and below 60 is considered poor. 6 weeks after surgery
Secondary Knee Society Score (KSS) at third month The collection of functional outcomes score KSS at third month. The Knee Society Score (KSS) is mixed outcome measure that's both objective (physician input) and subjective (patient input). A score between 80 and 100 is considered excellent, between 70 and 79 is considered good, between 60 and 69 is considered fair and below 60 is considered poor. third month after surgery
Secondary Knee Society Score (KSS) at sixth month The collection of functional outcomes score KSS at sixth month. The Knee Society Score (KSS) is mixed outcome measure that's both objective (physician input) and subjective (patient input). A score between 80 and 100 is considered excellent, between 70 and 79 is considered good, between 60 and 69 is considered fair and below 60 is considered poor. sixth month after surgery
Secondary Knee Society Score (KSS) at twelfth month The collection of functional outcomes score KSS at twelfth month. The Knee Society Score (KSS) is mixed outcome measure that's both objective (physician input) and subjective (patient input). A score between 80 and 100 is considered excellent, between 70 and 79 is considered good, between 60 and 69 is considered fair and below 60 is considered poor. twelfth month after surgery
Secondary Oxford Score (OS) at 6 weeks The collection of functional outcomes score OS at 6 weeks. The Oxford Score is a 12-item patient-reported outcomes (PRO) specifically designed and developed to assess function and pain after total knee replacement surgery. Each question is scored from 0 to 4 (0 being the worst outcome and 4 being the best). The overall score is the sum of all items and can range from 0 to 48, with higher scores corresponding to better outcomes. 6 weeks after surgery
Secondary Oxford Score (OS) at third month The collection of functional outcomes score OS at third month. The Oxford Score is a 12-item patient-reported outcomes (PRO) specifically designed and developed to assess function and pain after total knee replacement surgery. Each question is scored from 0 to 4 (0 being the worst outcome and 4 being the best). The overall score is the sum of all items and can range from 0 to 48, with higher scores corresponding to better outcomes. third month after surgery
Secondary Oxford Score (OS) at sixth month The collection of functional outcomes score OS at sixth month. The Oxford Score is a 12-item patient-reported outcomes (PRO) specifically designed and developed to assess function and pain after total knee replacement surgery. Each question is scored from 0 to 4 (0 being the worst outcome and 4 being the best). The overall score is the sum of all items and can range from 0 to 48, with higher scores corresponding to better outcomes. sixth month after surgery
Secondary Oxford Score (OS) at twelfth month The collection of functional outcomes score OS at twelfth month. The Oxford Score is a 12-item patient-reported outcomes (PRO) specifically designed and developed to assess function and pain after total knee replacement surgery. Each question is scored from 0 to 4 (0 being the worst outcome and 4 being the best). The overall score is the sum of all items and can range from 0 to 48, with higher scores corresponding to better outcomes. twelfth month after surgery
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