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Completed

NCT Number: NCT07736716

Arthroscopic Infrapatellar Fat Pad Release and Mesenchymal Stem Cell Mobilization

This prospective, single-center, paired-sample clinical laboratory study evaluated whether controlled mechanical release of the infrapatellar fat pad during knee arthroscopy increases the number of intra-articular cells with a mesenchymal stem cell immunophenotype. The study also evaluated whether the procedure is accompanied by immediate changes in the expression of selected genes associated with inflammation, immunomodulation, and tissue repair.

Adults undergoing knee arthroscopy for meniscal pathology had a 20-mL intra-articular fluid sample collected before manipulation of any intra-articular structure. The infrapatellar fat pad was then gently and selectively shaved for approximately 1 minute using a motorized arthroscopic shaver with the suction turned off. A second 20-mL intra-articular fluid sample was collected immediately after the procedure and before further irrigation or continuation of the planned arthroscopic surgery.

Paired pre-release and post-release samples were analyzed by flowcytometry to quantify cells with a mesenchymal stem cell immunophenotype. Quantitative real-time polymerase chain reaction was performed on the total cellular fraction to assess IL-1β, IL-6, IL-10, TGF-β, and CD24 gene expression. Comparisons were performed within each participant using the paired samples.

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Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ankara Bilkent City Hospital

Ankara, 06800, Turkey (Türkiye)

About this study

Cell-based orthobiologic strategies commonly require tissue harvesting from an extra-articular donor site, ex vivo processing, and subsequent intra-articular administration. The infrapatellar fatpad is a local intra-articular adipose tissue source containing cells with mesenchymal stem cell-related properties. However, it remains unclear whether cells with a mesenchymal stem cell immunophenotype can be directly mobilized into the joint fluid during routine knee arthroscopy and whether this mobilization is accompanied by an immediate molecular response.

This was a prospective, single-center, paired-sample clinical laboratory study involving adults undergoing routine knee arthroscopy for meniscal pathology. Participants were prospectively enrolled between January 2024 and January 2025. The study was designed as a within-participant comparison of paired intra-articular fluid samples collected immediately before and after controlled mechanical release of the infrapatellar fat pad.

Knee arthroscopy was performed through standard anterolateral and anteromedial portals. Sterile 0.9% saline was initially introduced to distend the joint and obtain adequate visualization. After visualization of the joint, fluid inflow was stopped, and no intra-articular structure was manipulated before baseline sampling. A 20-mL intra-articular fluid sample was aspirated using a sterile syringe and divided into two equal 10-mL aliquots as the pre-release sample.

Following baseline sampling, a motorized arthroscopic shaver was introduced through the anteromedial portal. With the shaver suction turned off, the infrapatellar fat pad was gently and selectively shaved for approximately 1 minute. Care was taken to avoid contact with the menisci, articular cartilage, cruciate ligaments, and synovial structures outside the intended release area.

Immediately after controlled mechanical release of the infrapatellar fat pad, and before further irrigation or continuation of the planned arthroscopic procedure, a second 20-mL intra-articular fluid sample was collected under the same conditions. This sample was divided into two equal 10-mL aliquots as the post-release sample. No additional fluid was introduced into the joint between the pre-release and post-release sampling procedures. After collection of the post-release sample, the released tissue was removed using routine arthroscopic suction and irrigation, and the planned arthroscopic procedure was completed.The timing, sample volume, portal use, release technique, and specimen handling were standardized across participants.

Paired samples were analyzed by flow cytometry using standardized processing and acquisition procedures. The final population selected for quantitative analysis was defined as LIN-negative, CD29-positive, CD73-positive, CD13-positive, CD105-positive, CD90-positive, and CD31-negative, representing cells with a mesenchymal stem cell immunophenotype.

Quantitative real-time polymerase chain reaction was performed separately on the total cellular fraction of each pre-release and post-release sample without flow cytometric sorting or enrichment of the mesenchymal stem cell-immunophenotype population. Expression levels of IL-1β, IL-6, IL-10, TGF-β, and CD24 were evaluated, with GAPDH used as the reference gene. Relative gene-expression changes were calculated using the comparative 2^-ΔΔCt method.

The primary objective was to compare the number of cells with a mesenchymal stem cell immunophenotype in standardized intra-articular samples collected before and after controlled mechanical release of the infrapatellar fat pad. The secondary objective was to compare the expression of the selected molecular markers between paired pre-release and post-release samples. The study evaluated immediate cellular and molecular changes and was not designed to assess the persistence, functional activity, or clinical efficacy of the mobilized cell population.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age between 18 and 55 years
  • Presence of knee pain
  • Meniscal tear confirmed by magnetic resonance imaging
  • Scheduled to undergo arthroscopic knee surgery
  • Provision of written informed consent to participate in the study

Exclusion criteria

  • Requirement for emergency surgery
  • Open injury involving the knee
  • Severe anterior or posterior cruciate ligament injury causing substantial knee instability
  • Tibial eminence fracture
  • Osteochondral defect requiring surgical treatment
  • Planned open knee surgery
  • Suspected septic arthritis
  • Inflammatory arthritis
  • Suspected intra-articular tumor
  • Previous arthroscopic surgery on the same knee
  • Declining to participate in the study

Treatment and study plan

Controlled Mechanical Release of the Infrapatellar Fat Pad

Procedure

After baseline intra-articular fluid sampling, the infrapatellar fat pad was gently and selectively shaved for approximately 1 minute with the motorized arthroscopic shaver suction temporarily turned off. A second intra-articular fluid sample was collected immediately after shaving and before further irrigation. The released tissue was subsequently removed using routine arthroscopic suction and irrigation. No released tissue or cells were intentionally retained in the joint for therapeutic purposes.

Primary outcomes

  1. Number of Cells With a Mesenchymal Stem Cell Immunophenotype Before and After Infrapatellar Fat Pad Release

    Time frame: Immediately before and immediately after the approximately 1-minute infrapatellar fat pad release procedure during the same knee arthroscopy

    The number of LIN-negative, CD29-positive, CD73-positive, CD13-positive, CD105-positive, CD90-positive, and CD31-negative cells was quantified by flow cytometry in standardized paired intra-articular fluid samples collected before and immediately after controlled mechanical release of the infrapatellar fat pad. Paired cell counts were summarized as median with minimum and maximum values and compared within participants.

Secondary outcomes

  1. Fold Change in IL-1β Gene Expression After Infrapatellar Fat Pad Release

    Time frame: Immediately before and immediately after the approximately 1-minute infrapatellar fat pad release procedure during the same knee arthroscopy

    IL-1β gene expression was measured by quantitative real-time polymerase chain reaction in the total cellular fraction of paired pre-release and post-release intra-articular samples. Expression was normalized to GAPDH, and relative change was calculated using the comparative 2^-ΔΔCt method and reported as fold change relative to the pre-release sample.

  2. Fold Change in IL-6 Gene Expression After Infrapatellar Fat Pad Release

    Time frame: Immediately before and immediately after the approximately 1-minute infrapatellar fat pad release procedure during the same knee arthroscopy

    IL-6 gene expression was measured by quantitative real-time polymerase chain reaction in the total cellular fraction of paired pre-release and post-release intra-articular samples. Expression was normalized to GAPDH, and relative change was calculated using the comparative 2^-ΔΔCt method and reported as fold change relative to the pre-release sample.

  3. Fold Change in IL-10 Gene Expression After Infrapatellar Fat Pad Release

    Time frame: Immediately before and immediately after the approximately 1-minute infrapatellar fat pad release procedure during the same knee arthroscopy

    IL-10 gene expression was measured by quantitative real-time polymerase chain reaction in the total cellular fraction of paired pre-release and post-release intra-articular samples. Expression was normalized to GAPDH, and relative change was calculated using the comparative 2^-ΔΔCt method and reported as fold change relative to the pre-release sample.

  4. Fold Change in TGF-β Gene Expression After Infrapatellar Fat Pad Release

    Time frame: Immediately before and immediately after the approximately 1-minute infrapatellar fat pad release procedure during the same knee arthroscopy

    TGF-β gene expression was measured by quantitative real-time polymerase chain reaction in the total cellular fraction of paired pre-release and post-release intra-articular samples. Expression was normalized to GAPDH, and relative change was calculated using the comparative 2^-ΔΔCt method and reported as fold change relative to the pre-release sample.

  5. Fold Change in CD24 Gene Expression After Infrapatellar Fat Pad Release

    Time frame: Immediately before and immediately after the approximately 1-minute infrapatellar fat pad release procedure during the same knee arthroscopy

    CD24 gene expression was measured by quantitative real-time polymerase chain reaction in the total cellular fraction of paired pre-release and post-release intra-articular samples. Expression was normalized to GAPDH, and relative change was calculated using the comparative 2^-ΔΔCt method and reported as fold change relative to the pre-release sample.

Sponsors and collaborators

Lead sponsor

Ankara City Hospital Bilkent

Other

Registry information

Official study title

Arthroscopic Mechanical Release of the Infrapatellar Fat Pad Mobilizes Cells With a Mesenchymal Stem Cell Immunophenotype and Alters Early Molecular Responses.

Acronym: IP-MSC-RELEASE

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Jul 30, 2026
Registry last updated
Jul 30, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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