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Trial Comparing Botulin Toxin Versus Hyaluronic Acid by Intra-articular Injection for the Treatment of Painful Knee Osteoarthritis (GOTOX)

Primary Purpose

Painful Unilateral Femorotibial Knee Osteoarthritis of Any Etiology

Status
Unknown status
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Botulinum toxin A ( BoNT-A)
Hyaluronic acid (HA)
Sponsored by
University Hospital, Strasbourg, France
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Painful Unilateral Femorotibial Knee Osteoarthritis of Any Etiology focused on measuring Knee osteoarthritis, Intra-articular botulinum toxin, Hyaluronic acid, Pain, Function

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Painful, or predominantly unilateral painful, knee osteoarthritis of any etiology
  • Knee without clinical signs of intra-articular effusion
  • Kellgren score ≥ II on X-ray
  • WOMAC pain sub-score ≥ 5 in the month preceding the inclusion visit

Exclusion Criteria:

Clinical:

  • Inflammatory arthropathy,infectious, neoplastic within the past year
  • Neuromuscular pathology
  • Cardiorespiratory pathology or any other severe disease that interferes with the functional capacities
  • Any decompensated or unstable chronic pathology
  • Glomerular filtration rate (GFR)<15 mL/min/1.73m²) within the past 6 months
  • HBA1c in diabetic people > 12% within the past 6 months
  • BMI ≥ 35kg/m2
  • Infection: joint, general, distant, cutaneous
  • Foreign material in the knee to be treated: prosthesis, osteosynthesis material
  • Severe coagulation problem: platelets <100000/mm3 within the past 6 months
  • Allergy to BoNT-A
  • Allergy to HA
  • Pregnant or breast-feeding women
  • Treatment with aminoglycosides or direct oral anticoagulants
  • Treatment with VKA (antihemorrhagic vitamin) if INR (International Normalized Ratio) higher than 3 within the past month
  • Change of anti-pain treatment less than 2 weeks before enrolment
  • Treatment with III pain killers or corticosteroids because of intense pain that does not respond to schedule I and II pain-killers
  • Intra-articular injection of corticosteroids in the previous two months
  • Viscosupplementation and/or injection of BoNT-A in the knee to be treated within the past 6 months
  • Injection of BoNT-A (except the knee to be treated) within the past 3 months
  • Swallowing troubles

Sites / Locations

  • Hôpitaux Universitaires de Strasbourg

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Intra-articular injection of botulinum toxin A

Intra-articular injection of hyaluronic acid

Arm Description

Outcomes

Primary Outcome Measures

Evaluation of pain measured using the WOMAC pain sub-score

Secondary Outcome Measures

Evaluation of the antalgic effect of BoNT-A vs hyaluronic acid measured using a verbal rating scale (VRS)
Evaluation of the patients' functional improvement based on the WOMAC score ("stiffness and function sub-score" and total score)
Evaluation of the patients' functional improvement using the Timed Up-and-go Test
Evaluation of the quality of life based on the SF-36 score
Frequency, seriousness and severity of adverse event reactions
Changes in pain treatment score (using a correspondence table)
Changes in muscular strenght et muscular trophicity (using dynanometer and measure of knee and thin circumference)
Changes in passive and active articular knee amplitude, by goniometry

Full Information

First Posted
May 27, 2016
Last Updated
September 13, 2021
Sponsor
University Hospital, Strasbourg, France
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1. Study Identification

Unique Protocol Identification Number
NCT02832713
Brief Title
Trial Comparing Botulin Toxin Versus Hyaluronic Acid by Intra-articular Injection for the Treatment of Painful Knee Osteoarthritis
Acronym
GOTOX
Official Title
Randomized Controlled Trial Comparing Botulin Toxin Versus Hyaluronic Acid by Intra-articular Injection for the Treatment of Painful Knee Osteoarthritis
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Unknown status
Study Start Date
June 9, 2017 (Actual)
Primary Completion Date
October 2021 (Anticipated)
Study Completion Date
December 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Strasbourg, France

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
In France, osteoarthritis affects about 10 million people and knee osteoarthritis represents 35% of cases. It is thought that more than 2.5 million people older than 65 years have knee osteoarthritis. Currently, osteoarthritis management is based on three major axes: Non-pharmacological means, such as patient education, loss of weight and physical activity General pharmacological treatments: mainly paracetamol and then schedule II and III painkillers as well as nonsteroidal anti-inflammatory agent. Intra-articular pharmacological treatments: Intra-articular injections of corticosteroids: they are recommended during hydarthrotic flare-ups Intra-articular injections of hyaluronic acid (HA) (viscosupplementation) in the absence of intra-articular effusion. However, their efficacy is questioned by most experts in the case of symptomatic knee osteoarthrosis. Sometimes, surgery is the only therapeutic option. However, besides the fact of exposing patients, who are sometimes frail, to several peri- and post-operative complications, the recovery rate (variable according to the prosthesis type and ranging from 5% to 25% at 9 years) in an ageing population justifies waiting as much as possible before surgery. Therefore, it is important to test new therapeutic options for symptomatic osteoarthrosis that will allow postponing the surgical treatment. The use of botulinum toxin (BoNT-A) could thus represents an interesting alternative. BoNT-A is habitually used by intra-muscular injection for its myorelaxant effect in the management of painful reactive periarticular muscle contractures. However, BoNT-A has also antalgic activity independently of the myorelaxant effect. This allows explaining in part the antalgic effect of intra-articular BoNT-A injection. In the literature, six randomized controlled studies (RCS) have compared BoNT-A and intra-articular injections of corticosteroids, hyaluronic acid, or placebo. Only two RCS concerned knee osteoarthritis and compared BoNT-A to corticosteroids and a placebo, respectively, with a significant antalgic effect only in the groups treated with BoNT-A. No study has compared yet the intra-articular injection of BoNT-A to the viscosupplementation by HA in knee osteoarthritis and this is the aim of this trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Painful Unilateral Femorotibial Knee Osteoarthritis of Any Etiology
Keywords
Knee osteoarthritis, Intra-articular botulinum toxin, Hyaluronic acid, Pain, Function

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intra-articular injection of botulinum toxin A
Arm Type
Experimental
Arm Title
Intra-articular injection of hyaluronic acid
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Botulinum toxin A ( BoNT-A)
Intervention Description
Intra-articular injection of BoNT-A
Intervention Type
Device
Intervention Name(s)
Hyaluronic acid (HA)
Intervention Description
Intra-articular injection of Hyaluronic acid
Primary Outcome Measure Information:
Title
Evaluation of pain measured using the WOMAC pain sub-score
Time Frame
Change from baseline WOMAC pain sub-score at 3 months
Secondary Outcome Measure Information:
Title
Evaluation of the antalgic effect of BoNT-A vs hyaluronic acid measured using a verbal rating scale (VRS)
Time Frame
1 week after injection
Title
Evaluation of the patients' functional improvement based on the WOMAC score ("stiffness and function sub-score" and total score)
Time Frame
Before injection, 1 month, 3 months and 6 months following injection
Title
Evaluation of the patients' functional improvement using the Timed Up-and-go Test
Time Frame
Before injection, 1 month, 3 months and 6 months following injection
Title
Evaluation of the quality of life based on the SF-36 score
Time Frame
Before injection, 1 month, 3 months and 6 months following injection
Title
Frequency, seriousness and severity of adverse event reactions
Time Frame
during the 6 months following injection
Title
Changes in pain treatment score (using a correspondence table)
Time Frame
Change from baseline pain treatment score at 6 months
Title
Changes in muscular strenght et muscular trophicity (using dynanometer and measure of knee and thin circumference)
Time Frame
Before injection, 1 month, 3 months and 6 months following injection
Title
Changes in passive and active articular knee amplitude, by goniometry
Time Frame
Before injection, 1 month, 3 months and 6 months following injection

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Painful, or predominantly unilateral painful, knee osteoarthritis of any etiology Knee without clinical signs of intra-articular effusion Kellgren score ≥ II on X-ray WOMAC pain sub-score ≥ 5 in the month preceding the inclusion visit Exclusion Criteria: Clinical: Inflammatory arthropathy,infectious, neoplastic within the past year Neuromuscular pathology Cardiorespiratory pathology or any other severe disease that interferes with the functional capacities Any decompensated or unstable chronic pathology Glomerular filtration rate (GFR)<15 mL/min/1.73m²) within the past 6 months HBA1c in diabetic people > 12% within the past 6 months BMI ≥ 35kg/m2 Infection: joint, general, distant, cutaneous Foreign material in the knee to be treated: prosthesis, osteosynthesis material Severe coagulation problem: platelets <100000/mm3 within the past 6 months Allergy to BoNT-A Allergy to HA Pregnant or breast-feeding women Treatment with aminoglycosides or direct oral anticoagulants Treatment with VKA (antihemorrhagic vitamin) if INR (International Normalized Ratio) higher than 3 within the past month Change of anti-pain treatment less than 2 weeks before enrolment Treatment with III pain killers or corticosteroids because of intense pain that does not respond to schedule I and II pain-killers Intra-articular injection of corticosteroids in the previous two months Viscosupplementation and/or injection of BoNT-A in the knee to be treated within the past 6 months Injection of BoNT-A (except the knee to be treated) within the past 3 months Swallowing troubles
Facility Information:
Facility Name
Hôpitaux Universitaires de Strasbourg
City
Strasbourg
ZIP/Postal Code
67091
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Trial Comparing Botulin Toxin Versus Hyaluronic Acid by Intra-articular Injection for the Treatment of Painful Knee Osteoarthritis

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