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Saline Lavage X Saline Lavage and Osteonil® Mini in Rizarthritis

Primary Purpose

Rhizarthrosis, Metabolic Disease

Status
Unknown status
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Visual Analog Scale (VAS)
Range of Motion (ROM)
Palmar grip strength
Lateral grip strength
Pulp-pulp pinch strength
Lavage with physiologic saline solution
Lavage with physiologic saline solution and Osteonil® Mini
Quick Dash
Sollerman Test
Sponsored by
University of Sao Paulo General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rhizarthrosis focused on measuring carpometacarpal joint ostearthritis, hyaluronic acid, Rhizarthrosis

Eligibility Criteria

40 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Men and women diagnosed with multiple arthritis (including CMC OA of the thumb) with comorbidities (metabolic syndrome, i.e., OA and overweight / obesity, and/or hyperglycemia, and/or dyslipidemia, and/or hyperuricemia, and/or hypertension).
  • CMC OA joint of the thumb stages I to III as classified by Eaton et al. (4)

Exclusion Criteria:

  • Missing classes or functional evaluations
  • Not performing the exercises as instructed

Sites / Locations

  • Instituto de Ortopedia e Traumatologia

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Lavage with Saline (LS)

Lavage with Osteonil® Mini (LO)

Arm Description

Under sterile conditions, the 1st carpometacarpal (CMC) will be locally anesthetized with ropivacaine and will be submitted to joint lavage with physiologic saline solution 2 to 5 mL (injection with a 30x8 needle and drained with the same needle after removal of the syringe. After emptying of the joint, 1mL saline solution will be injected. Patients will ask to answer Visual Analog Scale (VAS) questionnaire, Range of Motion (ROM), Quick DASH, Sollerman Test, and functional grip strength (palmar grip strength, lateral grip strength and pulp-pulp pinch strength) evaluations immediately prior to the procedure and after 1, 3 and 6 months of each joint.

Under sterile conditions, the 1st carpometacarpal (CMC) will be locally anesthetized with ropivacaine and will be submitted to lavage with physiologic saline solution and Osteonil® Mini 1mL of 10mg will be injected in the 1st CMC joint. Patients will ask to answer Visual Analog Scale (VAS) questionnaire, Range of Motion (ROM), Quick DASH, Sollerman Test, and functional grip strength (palmar grip strength, lateral grip strength and pulp-pulp pinch strength) evaluations immediately prior to the procedure and after 1, 3 and 6 months of each joint.

Outcomes

Primary Outcome Measures

Improvement in grip strength at 6 months
Perform test and collected data in baseline, 1 month, 3 months and 6 months.

Secondary Outcome Measures

Assess improvement in pain
Answer VAS (Visual Analog Scale)
Assess improvement in range of motion
Measure range of motion
Assess improvement in palmar grip strength
Perform palmar grip strength
Assess improvement in lateral pinch strength.
Perform lateral pinch strength.
Assess improvement in Pulp-pulp pinch strength
Perform pulp-pulp pinch strength

Full Information

First Posted
January 12, 2017
Last Updated
May 15, 2019
Sponsor
University of Sao Paulo General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03089723
Brief Title
Saline Lavage X Saline Lavage and Osteonil® Mini in Rizarthritis
Official Title
Comparative Study of the Intraarticular Treatment of Carpometacarpal Joint Ostearthritis of the Thumb With Lavage With Saline Solution, or Lavage and Injection of Hyaluronic Acid and Mannitol.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2019
Overall Recruitment Status
Unknown status
Study Start Date
March 30, 2017 (Actual)
Primary Completion Date
March 30, 2018 (Actual)
Study Completion Date
August 30, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sao Paulo General Hospital

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
Although a common problem, hand osteoarthritis (HOA) is less studied than knee and hip. In the age group of 71-100 years, the prevalence of symptomatic HOA reaches 26% of women and 13% of men. These patients lose hand strength and have difficulty with day-to-day manual activities. The main joints involved are the proximal and distal interphalangeals and the carpometacarpal joint of the thumb. In the educational Project PARQVE, the prevalence of HOA was 23.7% at inclusion in the program, and 47.4% after one year, with loss of grip strength. There is controversy over the effect of viscosupplementation in the treatment of rhizarthritis when considering pain. However, strength is a very important function parameter that must be evaluated for function and quality of life maintenance. Concerned about the importance of maintaining strength and function in our program (PARQVE), we have added specific exercises tom improve hand strength and range of motion. Trying to optimize the treatment and confronting questions about the effect of the joint wash, called placebo in the comparative studies with corticosteroid and/or hyaluronic acid injection, we did a work where all the patients will be washed with physiological saline solution but a group, after emptying, will receive 1mL of hyaluronic acid with mannitol. PURPOSE: To compare isolated lavage with lavage followed by injection of hyaluronic acid with mannitol into carpometacarpal osteoarthritis joint of the thumb. METHODS: Forty joints of patients with multiple osteoarthritis (rhizoarthritis, including) and comorbidities (two or more of: overweight or obesity, hyperglycemia, dyslipidemia, hyperuricemia, hypertension) will be allocated into two groups: Lavage (LS) and Lavage and Injection Hilauronic acid (LO). Both groups will undergo joint lavage with saline solution. The LO group will receive the 20 mg / mL hilauronic acid injection with 5mg mannitol. Both groups will be guided in the clinical treatment of osteoarthritis and metabolic syndrome and will be given daily exercises for the hands. They will be evaluated with the quick DASH questionnaire, Sollerman Test and by measuring the palmar, lateral and pulp-pulp grip strength, in addition to measuring the ROM and VAS pain moments immediately prior to the procedure, one, three and six months after the articular procedure.
Detailed Description
Patients with multiple osteoarthritis (including carpometacarpal joint of the thumb, stages I to III - Eaton et al.) in treatment at the Institute of Orthopedics and Traumatology fo the Clinics Hospital - University of São Paulo (IOT-HC-FMUSP) will be invited to participate in this study. All patients are obliged to participate in a two-day education course on OA. During the program they are instructed about OA, metabolic syndrome, comorbidities and importance of diet, and daily exercise (including specific exercises for the hand). After inclusion, 40 joints will be randomized in one of two treatment options, i.e., Lavage with saline solution and final injection of 1mL of saline solution, or lavage with saline solution followed by injection of 10mg of hyaluronic acid with mannitol (5mg). After the procedure patients will receive naproxen 500mg twice daily for 5 days. Patients will be instructed to exercise at least 180 minutes/week and if possible daily exercise for the hand (5 to 10 minutes daily). Patients will be instructed to write down when and what they exercised as well as their daily medication intake (for co-morbidities and pain). All patients will be submitted to pain (VAS), range of motion (ROM), Quick DASH, Sollermand Test and functional (palmar grip strength and lateral and pulp-pulp pinch strength) evaluations immediately prior to the procedure and after 1, 3 and 6 months of each joint. As the assessments of pain, range of motion and strength will be compared with measurements of the same limb at inclusion, each hand involved of the patient will be considered as a case. The "n" was calculated to obtain a statistical power of 80% and a level of significance of 5%. To do this, we considered the mean and standard deviation of the pulp-pulp pinch (our primary outcome) found in previous study of the prevalence of hand OA in individuals with knee osteoarthritis submitted to our educational program. A sample size was used to detect a variation of 1 point on the two-tailed pulp-pulp pinches. The sample size calculated by group was 16. Considering also possible faults and abandon of about 20% of the patients, the value of 20 patients per group was obtained.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rhizarthrosis, Metabolic Disease
Keywords
carpometacarpal joint ostearthritis, hyaluronic acid, Rhizarthrosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Lavage with Saline (LS)
Arm Type
Experimental
Arm Description
Under sterile conditions, the 1st carpometacarpal (CMC) will be locally anesthetized with ropivacaine and will be submitted to joint lavage with physiologic saline solution 2 to 5 mL (injection with a 30x8 needle and drained with the same needle after removal of the syringe. After emptying of the joint, 1mL saline solution will be injected. Patients will ask to answer Visual Analog Scale (VAS) questionnaire, Range of Motion (ROM), Quick DASH, Sollerman Test, and functional grip strength (palmar grip strength, lateral grip strength and pulp-pulp pinch strength) evaluations immediately prior to the procedure and after 1, 3 and 6 months of each joint.
Arm Title
Lavage with Osteonil® Mini (LO)
Arm Type
Experimental
Arm Description
Under sterile conditions, the 1st carpometacarpal (CMC) will be locally anesthetized with ropivacaine and will be submitted to lavage with physiologic saline solution and Osteonil® Mini 1mL of 10mg will be injected in the 1st CMC joint. Patients will ask to answer Visual Analog Scale (VAS) questionnaire, Range of Motion (ROM), Quick DASH, Sollerman Test, and functional grip strength (palmar grip strength, lateral grip strength and pulp-pulp pinch strength) evaluations immediately prior to the procedure and after 1, 3 and 6 months of each joint.
Intervention Type
Behavioral
Intervention Name(s)
Visual Analog Scale (VAS)
Intervention Description
Answer Visual Analog Scale (VAS) questionnaire at baseline, 1 month, 3 months and 6 months
Intervention Type
Behavioral
Intervention Name(s)
Range of Motion (ROM)
Intervention Description
submitted to ROM at at baseline, 1 month, 3 months and 6 months
Intervention Type
Behavioral
Intervention Name(s)
Palmar grip strength
Intervention Description
submitted to palmar grip strength at at baseline, 1 month, 3 months and 6 months
Intervention Type
Behavioral
Intervention Name(s)
Lateral grip strength
Intervention Description
submitted to lateral grip strength at at baseline, 1 month, 3 months and 6 months
Intervention Type
Behavioral
Intervention Name(s)
Pulp-pulp pinch strength
Intervention Description
submitted to pulp-pulp pinch strength strength at at baseline, 1 month, 3 months and 6 months
Intervention Type
Drug
Intervention Name(s)
Lavage with physiologic saline solution
Other Intervention Name(s)
Lavage with Saline (LS)
Intervention Description
Joint lavage with physiologic saline solution. After emptying of the joint, 1mL saline solution will be injected.
Intervention Type
Drug
Intervention Name(s)
Lavage with physiologic saline solution and Osteonil® Mini
Other Intervention Name(s)
Lavage with Osteonil® Mini (LO)
Intervention Description
Joint lavage with physiologic saline solution and Osteonil® Mini
Intervention Type
Behavioral
Intervention Name(s)
Quick Dash
Intervention Description
Answer Quick Dash questionnaire at baseline, 1 month, 3 months and 6 months
Intervention Type
Behavioral
Intervention Name(s)
Sollerman Test
Intervention Description
Perform Sollerman Test at baseline, 1 month, 3 months and 6 months
Primary Outcome Measure Information:
Title
Improvement in grip strength at 6 months
Description
Perform test and collected data in baseline, 1 month, 3 months and 6 months.
Time Frame
Baseline, 1 month, 3 months and 6 months.
Secondary Outcome Measure Information:
Title
Assess improvement in pain
Description
Answer VAS (Visual Analog Scale)
Time Frame
Baseline, 1 month, 3 months and 6 months.
Title
Assess improvement in range of motion
Description
Measure range of motion
Time Frame
Baseline, 1 month, 3 months and 6 months.
Title
Assess improvement in palmar grip strength
Description
Perform palmar grip strength
Time Frame
Baseline, 1 month, 3 months and 6 months.
Title
Assess improvement in lateral pinch strength.
Description
Perform lateral pinch strength.
Time Frame
Baseline, 1 month, 3 months and 6 months.
Title
Assess improvement in Pulp-pulp pinch strength
Description
Perform pulp-pulp pinch strength
Time Frame
Baseline, 1 month, 3 months and 6 months.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men and women diagnosed with multiple arthritis (including CMC OA of the thumb) with comorbidities (metabolic syndrome, i.e., OA and overweight / obesity, and/or hyperglycemia, and/or dyslipidemia, and/or hyperuricemia, and/or hypertension). CMC OA joint of the thumb stages I to III as classified by Eaton et al. (4) Exclusion Criteria: Missing classes or functional evaluations Not performing the exercises as instructed
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marcia U Rezende, MD; PhD
Organizational Affiliation
Department of Orthopedics and Traumatology - HCFMUSP
Official's Role
Principal Investigator
Facility Information:
Facility Name
Instituto de Ortopedia e Traumatologia
City
São Paulo
State/Province
SP
ZIP/Postal Code
05403010
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
No
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Saline Lavage X Saline Lavage and Osteonil® Mini in Rizarthritis

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