NCT05450458

Brief Summary

Sports activity represents part of day living people, a knee pain originated by high demand joint activity could represent a limitation to continue sports. The aim of this clinical trial is demonstrate the effects of hyaluronic acid in sportsmen with knee pain.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
64

participants targeted

Target at P50-P75 for phase_2

Timeline
Completed

Started Feb 2023

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 17, 2022

Completed
21 days until next milestone

First Posted

Study publicly available on registry

July 8, 2022

Completed
7 months until next milestone

Study Start

First participant enrolled

February 1, 2023

Completed
1.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 30, 2024

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2025

Completed
3 months until next milestone

Results Posted

Study results publicly available

July 22, 2025

Completed
Last Updated

July 22, 2025

Status Verified

July 1, 2025

Enrollment Period

1.7 years

First QC Date

June 17, 2022

Results QC Date

April 22, 2025

Last Update Submit

July 1, 2025

Conditions

Keywords

KNEEPAINSPORTSMENHYALURONIC ACID

Outcome Measures

Primary Outcomes (2)

  • Efficacy of Hyaluronic Acid With Sorbitol (SYNOLIS VA) in Overuse Knee Syndrome Assessed With the Knee Injury and Osteoarthritis Outcome Score (KOOS)

    To demonstrate that two doses of intra-articular injection of Synolis VA® for the overuse knee syndrome in sportsmen decrease the pain during spots and day-living activities by measured the improvement of knee symptoms through the KOOS score: \- The Knee injury and Osteoarthritis Outcome Score: Evaluate Symptoms + Stiffness subtotal, Pain, Function, daily living, sports and recreational activities and quality of life. Each variable has a percentage score from 0 to 100%, at the end the results are averaged, obtaining a final percentage where 100% means a healthy knee with out discomfort. As the percentage approaches 0%, the severity of knee discomfort or injury increases.

    Baseline, 15 days, 3 months, and 6 months

  • Efficacy of Hyaluronic Acid With Sorbitol (SYNOLIS VA) in Overuse Knee Syndrome Assessed With the International Knee Documentation Committee Score (IKDC)

    To evaluate the effectiveness of two intra-articular injections of Synolis VA in improving knee functionality in athletes with overuse knee syndrome, the International Knee Documentation Committee (IKDC) Scale was used. This validated tool assesses knee function, symptoms, and the ability to perform sports-related activities. It consists of individual items evaluating pain, stiffness, swelling, instability, daily physical function, and athletic performance. While the scale's raw score ranges from 0 to 87, results are converted into a percentage format, where 87 corresponds to 100% functional capacity-the best possible knee function-and 0 represents the worst condition."

    Baseline, 15 days, 3 months, and 6 months

Secondary Outcomes (2)

  • Safety of Hyaluronic Acid With Sorbitol (SYNOLIS VA ®) in Overuse Knee Syndrome by the Number of Adverse Effects in Participants.

    6 months

  • Six-Month Functional Improvement in Knee Function (IKDC and KOOS) in Athletes With Overuse Knee Syndrome With Elevated BMI Following Synolis VA Injections

    6 months post-treatment

Study Arms (1)

Hyaluronic Acid group

EXPERIMENTAL

All overuse knee syndrome participants after both knee joint infiltration with two doses each of Synolis VA (2ml = 40 milligrams of hyaluronic acid with 80 milligrams of sorbitol).

Drug: KNEE JOINT INFILTRATION WITH HYALURONIC ACID WITH SORBITOL SYNOLIS VA

Interventions

KNEE INFILTRATION WITH HYALURONIC ACID WITH SORBITOL IN SPORTSMEN

Also known as: VISCOSUPPLEMENTATION WITH SYNOLIS VA
Hyaluronic Acid group

Eligibility Criteria

Age30 Years - 55 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • \- Patients with knee pain for more than 3 months
  • Patients between 30 and 55 years old
  • Patients without a history of previous knee joint surgery.
  • Patients without chronic-degenerative diseases such as diabetes, hypertension, rheumatoid arthritis or other autoimmune diseases.
  • Patients who perform impact social sports at least 3 times a week for more than 1 hour in the last 3 months prior to treatment.
  • Patients without a history of allergies to non-steroidal anti-inflammatory drugs.
  • Patients with no history of infection in or around the knee.

You may not qualify if:

  • \- Patients who cannot be categorized as social athletes.
  • Patients with an associated sports injury that limits their sports practice.
  • Patients who have a treatment associated with knee pain independent of that established in the study protocol.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Issemym Tlalnepantla

Tlanepantla, 54055, Mexico

Location

Related Publications (34)

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    PMID: 3741515BACKGROUND
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    PMID: 22068268BACKGROUND
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    PMID: 26069577BACKGROUND
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  • Demange MK, Sisto M, Rodeo S. Future trends for unicompartmental arthritis of the knee: injectables & stem cells. Clin Sports Med. 2014 Jan;33(1):161-74. doi: 10.1016/j.csm.2013.06.006. Epub 2013 Jul 19.

    PMID: 24274853BACKGROUND
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Related Links

MeSH Terms

Conditions

Cumulative Trauma DisordersPain

Interventions

Hyaluronic AcidViscosupplementation

Condition Hierarchy (Ancestors)

Sprains and StrainsWounds and InjuriesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

GlycosaminoglycansPolysaccharidesCarbohydratesInjections, Intra-ArticularInjectionsDrug Administration RoutesDrug TherapyTherapeuticsOrthopedic Procedures

Results Point of Contact

Title
Dr. Julio Carlos Vélez de Lachica
Organization
RodillaActiva Medical Center

Publication Agreements

PI is Sponsor Employee
No
Restrictive Agreement
No

Study Design

Study Type
interventional
Phase
phase 2
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: A study group will be integrated which will be evaluated before the intervention and after 15 days, 3 and 6 subsequent months.
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Head of orthopedic surgery department

Study Record Dates

First Submitted

June 17, 2022

First Posted

July 8, 2022

Study Start

February 1, 2023

Primary Completion

October 30, 2024

Study Completion

April 30, 2025

Last Updated

July 22, 2025

Results First Posted

July 22, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

Locations