Gluteal Muscles, Gluteal Tendinitis, Greater Trochanteric Pain Syndrome, GTPS - Greater Trochanteric Pain Syndrome, Pertrochanteric Fracture, Tendon Disorder
Conditions
Keywords
MD-Tissue Collagen Medical, Ecoguide, Biomechanical, Modified Harris Hip Score, Numeric Rating Scale, Type I collagen
Brief summary
Greater Trochanteric Pain Syndrome, also known as GTPS (Greater Trochanteric Pain Syndrome) is a complex clinical condition characterized by chronic and recurrent pain in the lateral region of the hip, near the greater trochanter of the femur. Biomechanical and anatomic-histologic interactions of the structures of the peri trochanteric space, in which, given the close anatomic-functional relationships, the origin can be traced to three different pathologic entities that may influence each other and fuel the progressive exacerbation of symptomatology. These are: external snap hip, trochanteric bursitis, and tendinopathies of the tendons of the gluteus mediums and gluteus minimums muscles. Recent studies regarding GTPS have shown that in most cases this condition is due to degenerative tendinopathy of the tendons of the gluteus minimums and gluteus mediums muscles. Tendinopathy is defined as a pathological condition associated with histological changes that may result in a change in the organization of collagen fibrils, relative increase in the percentage of proteoglycans, glycosaminoglycans, and no collagenous components of the ECM accompanied by neo-vascularization and inflammatory state. Tendinopathies thus result in painful symptomatology that very often also results in biomechanical functional deficit. Clinically, GTPS presents as pain that is often debilitating and exacerbated by activities such as walking, climbing stairs, and lying on the affected side at night, associated with a progressive loss of stenia in hip abduction movements. On objective examination, a point of tenderness (trigger point) is noted at the level of the region of the greater trochanter, which may radiate to the lumbar area and along the lateral aspect of the thigh to the ipsilateral knee and a difficulty on strength versus resistance tests in hip abduction movements. Although it is a very common syndrome, the treatment of painful grand trochanter syndrome, as well as that of tendinopathies in general, is still a major hurdle because the specific cellular pathogenetic and biomechanical etiopathogenetic mechanisms are still partly unknown and many treatments are empirical. Traditionally, the treatment of GTPS is initially conservative and includes rest, ice, NSAIDs and physiotherapy with stretching exercises of the fascia late. The use of corticosteroids, with systemic or local infiltrative intake, for the treatment of tendinopathies is highly controversial and, in any case, does not seem to have long-term efficacy. MD-Tissue Collagen Medical Device is an injectable medical device based on porcine collagen type I; the collagen content is 100µg/2mL. Porcine collagen is like human collagen and highly compatible; it has very low risks of inducing adverse effects and is therefore used in several clinical settings.
Detailed description
This is a pilot monocentric Clinical Investigation based on a One sample design. In the ex vivo study, MD-Tissue Collagen Medical Device was used as a substrate for cell cultures of human gluteal tenocytes on culture plates. The results suggest how MD-Tissue can induce an anabolic phenotype in tenocytes by stimulating their proliferation and migration; it would also be able to promote the synthesis, maturation, and secretion of COL-I, thereby promoting tendon homeostasis and repair. Specifically, the modification of gene expression and proteins involved in collagen turnover pathways were analyzed by real-time PCR, Slot blot and SDS-zymography. Data from the study showed that tenocytes cultured with MD-Tissue compared with controls exhibited increased secretion and migration of COL-1 increased mRNA levels of the matrix metalloprotease inhibitor proteins MMP-1 and TIMP-1. The tenocytes used for the cell cultures were gluteal tenocytes, derived from human gluteal tendon fragments (obtained from subjects without any tendon pathology who had undergone total hip replacement surgery); therefore, it is reasonable to think that the porcine type I collagen-based compound may be a viable treatment in GTPS. The results of the preclinical study suggest how MD-Tissue Collagen Medical Device can induce an anabolic phenotype in tenocytes by stimulating tenocyte proliferation and COL-I synthesis, maturation, and secretion, thereby promoting tendon repair. As these effects have been evaluated ex vivo on tenocytes of gluteal muscle tendons, the purpose of this study is to evaluate its efficacy in local infiltrative treatment, in the pertechnetic region, of GTPS, in terms of resolution of pain symptoms and recovery of stenia in abduction. Variables will be assessed at 6 different times; at baseline (day 0), after week 1, weeks 2, weeks 6, weeks 10 and after weeks 24.
Interventions
The Experimental Group will be treated with 2-mL volume ultrasound-guided infiltration of: MD-Tissue (GUNA, Milan-Italy). Composition for 2 ml: collagen 100 micrograms Subjects will be treated with No.1 infiltration per week for 3 consecutive weeks. The infiltrations will be performed in an echoguided mode. MD-Tissue Collagen Medical Device will be infiltrated into the trochanteric bursa and at the level of the tendons of the gluteus minimus and gluteus medius, particularly at the level of the most degenerated insertional areas.
Sponsors
Study design
Intervention model description
One sample study
Eligibility
Inclusion criteria
* Male and female subjects aged 18 to 70 years; * subjects with lateral palpatory pain that has appeared for at least 1 month; * subjects with hip pain symptomatology assessed by Numerical rating scale (NRS) ≥ to 5; * Subjects able to cooperate for the assessments in the Survey plan; * subjects able to understand and sign informed consent.
Exclusion criteria
* subjects with true coxalgia (with positive FADDIR); * subjects with ESHS (external snap hip syndrome); * subjects already undergoing candidate hip replacement surgery; * subjects with radiologic and clinical evidence of small and/or middle gluteal tendon detachment with indication for surgical repair; * subjects with evidence of radiographically documented tendon calcifications; * subjects with a degree of coxarthrosis of the hip that is a candidate for treatment according to the classification of Tonnis\>1 * subjects who have taken fluoroquinolones within 30 days prior to enrollment * subjects who have undergone treatment with hyaluronic acid or corticosteroids in the hip candidate for infiltrative treatment within 4 weeks before enrollment; * subjects with local infections of the treatment candidate hip or systemic infections, osteomyelitis, or sepsis; * subjects on chronic treatment with corticosteroids or immunosuppressants; * subjects who are drug addicts, alcoholics, have psychiatric disorders, or have clinical conditions that may compromise the correct interpretation of PROMs or follow-up; * subjects with coagulopathies, platelet aggregation disorders, or on treatment with oral anticoagulants or antiplatelets that cannot be discontinued during the study period; * Pregnant and lactating subjects (female subjects of childbearing age should be tested for pregnancy before enrollment); * subjects with allergy to porcine collagen.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in NRS (Numerical Rating Scale) Pain Score From Baseline (Week 0) to Week 10 | weeks 10 | Pain intensity was measured using the NRS (Numerical Rating Scale), a validated scale ranging from 0 (no pain) to 10 (worst possible pain). Participants were asked to indicate their pain level at baseline (Week 0) and at Week 10. A change of at least 3 points on the NRS is considered clinically significant. The primary outcome is the mean change in NRS score from baseline to Week 10. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in Modified Harris Hip Score (mHHS) From Baseline to Weeks 6, 10, and 24 | Weeks 6, 10, and 24 | The Modified Harris Hip Score (mHHS) is a validated tool for assessing hip function and pain. It ranges from 0 (worst functional outcome and highest pain) to 100 (best function and least pain). Participants were evaluated at Weeks 6, 10, and 24 compared to baseline. The change in total score is used to assess clinical improvement. Unit of Measure: Score from 0 to 100; higher scores indicate better outcome |
| Change in Hip Abduction Strength From Baseline to Weeks 6, 10, and 24 | Weeks 6, 10, and 24 | Hip abduction strength was assessed using a handheld dynamometer at Weeks 6, 10, and 24. The measurement was performed with the patient standing on the contralateral (healthy) limb, while abducting the hip affected by GTPS. For each assessment, three consecutive measurements were taken and averaged. Results were compared to baseline (Day 0) to evaluate functional improvement in muscular strength. |
| Mean NRS (Numerical Rating Scale) Pain Score at Week 6 and Week 24 Compared to Baseline (T0) | weeks 6 and weeks 24 | Pain intensity was measured using the NRS (Numerical Rating Scale) at rest, ranging from 0 (no pain) to 10 (worst possible pain). Participants were asked to rate their pain at baseline (T0), week 6 (T6w/FU), and week 24 (T24w/FU). This outcome reports the mean NRS values at week 6 and 24. Higher scores indicate more intense pain. |
| Change in Analgesic Drug Consumption (Paracetamol and/or Celecoxib) From Baseline to Week 24 | Week 1, Week 2, Week 6, Week 10, and Week 24 compared to baseline (Week 0) Week 1, Week 2, Week 6, Week 10, and Week 24 compared to baseline (Week 0) Week 1, Week 2, Week 6, Week 10, and Week 24 compared to baseline (Week 0) | Analgesic drug consumption (paracetamol and/or celecoxib) was recorded using a patient diary at time points T0 (baseline), T1w, T2w, T6w/FU, T10w/FU, and T24w/FU. Each patient logged the number of analgesic doses consumed per week. The total number of doses per timepoint was used to assess any significant change over time. The analysis aimed to evaluate whether the treatment reduced the need for pain medication, as an indirect marker of clinical efficacy. Unit of measure: Number of analgesic doses consumed per week. |
| Incidence of Adverse Events (AE, SAE, SUSAR) From Baseline to Week 24 | Day 0 to Week 24 | Adverse events (AEs), serious adverse events (SAEs), and suspected unexpected serious adverse reactions (SUSARs) were monitored at each study visit from baseline (Day 0) to Week 24. Data were collected via systematic interviews and clinical assessments. No adverse events of any type were reported during the study. AE definitions followed ICH-GCP and ClinicalTrials.gov guidance. |
| MRI Evaluation of Inflammatory and Degenerative Signs in the Peritrochanteric Region at Week 24 Compared to Baseline | Week 24 compared to baseline (Week 0) | MRI evaluation focused on inflammatory and degenerative signs in the peritrochanteric region (gluteus medius/minimus tendons) was conducted at Week 24 and compared to baseline (Week 0). Two independent radiologists assessed peri-tendinous fluid and intra-tendinous edema on STIR-weighted images. Improvement was defined as visible reduction in peritendinous edema. The analysis was qualitative and dichotomous (Improved vs. Unchanged). |
Countries
Italy
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| MD-Tissue Medical Device MD Tissue Collagen Medical Device: The Experimental Group will be treated with 2-mL volume ultrasound-guided infiltration of: MD-Tissue (GUNA, Milan-Italy). Composition for 2 ml: collagen 100 micrograms Subjects will be treated with No.1 infiltration per week for 3 consecutive weeks. The infiltrations will be performed in an echoguided mode.
MD-Tissue Collagen Medical Device will be infiltrated into the trochanteric bursa and at the level of the tendons of the gluteus minimus and gluteus medius, particularly at the level of the most degenerated insertional areas. | 47 |
| Total | 47 |
Withdrawals & dropouts
| Period | Reason | FG000 |
|---|---|---|
| Overall Study | 4 drop out and one withdrawn | 5 |
Baseline characteristics
| Characteristic | MD-Tissue Medical Device | — |
|---|---|---|
| Age, Categorical <=18 years | 0 Participants | — |
| Age, Categorical >=65 years | 0 Participants | — |
| Age, Categorical Between 18 and 65 years | 47 Participants | — |
| Race and Ethnicity Not Collected | — | — Participants |
| Sex: Female, Male Female | 42 Participants | — |
| Sex: Female, Male Male | 5 Participants | — |
Adverse events
| Event type | EG000 affected / at risk |
|---|---|
| deaths Total, all-cause mortality | 0 / 43 |
| other Total, other adverse events | 0 / 43 |
| serious Total, serious adverse events | 0 / 43 |
Outcome results
Change in NRS (Numerical Rating Scale) Pain Score From Baseline (Week 0) to Week 10
Pain intensity was measured using the NRS (Numerical Rating Scale), a validated scale ranging from 0 (no pain) to 10 (worst possible pain). Participants were asked to indicate their pain level at baseline (Week 0) and at Week 10. A change of at least 3 points on the NRS is considered clinically significant. The primary outcome is the mean change in NRS score from baseline to Week 10.
Time frame: weeks 10
Population: All variables will be subjected to the appropriate descriptive analyses after validation of the input data. Continuous variables: mean ± standard deviation or median and range, depending on the distribution; categorical variables: absolute and relative frequency tables.
| Arm | Measure | Value (MEAN) |
|---|---|---|
| MD Tissue Collagen Medical Device | Change in NRS (Numerical Rating Scale) Pain Score From Baseline (Week 0) to Week 10 | 4.7 NRS Pain Score (range 0-10; higher score |
Change in Analgesic Drug Consumption (Paracetamol and/or Celecoxib) From Baseline to Week 24
Analgesic drug consumption (paracetamol and/or celecoxib) was recorded using a patient diary at time points T0 (baseline), T1w, T2w, T6w/FU, T10w/FU, and T24w/FU. Each patient logged the number of analgesic doses consumed per week. The total number of doses per timepoint was used to assess any significant change over time. The analysis aimed to evaluate whether the treatment reduced the need for pain medication, as an indirect marker of clinical efficacy. Unit of measure: Number of analgesic doses consumed per week.
Time frame: Week 1, Week 2, Week 6, Week 10, and Week 24 compared to baseline (Week 0) Week 1, Week 2, Week 6, Week 10, and Week 24 compared to baseline (Week 0) Week 1, Week 2, Week 6, Week 10, and Week 24 compared to baseline (Week 0)
Population: All participants who returned complete analgesic diaries at each visit (Weeks 1, 2, 6, 10, and 24) were included in the analysis.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| MD Tissue Collagen Medical Device | Change in Analgesic Drug Consumption (Paracetamol and/or Celecoxib) From Baseline to Week 24 | Week 1 | 1.6 Units of analgesics consumed (number of | Standard Deviation 1.8 |
| MD Tissue Collagen Medical Device | Change in Analgesic Drug Consumption (Paracetamol and/or Celecoxib) From Baseline to Week 24 | Week 2 | 0.8 Units of analgesics consumed (number of | Standard Deviation 1.4 |
| MD Tissue Collagen Medical Device | Change in Analgesic Drug Consumption (Paracetamol and/or Celecoxib) From Baseline to Week 24 | Week 6 | 0.5 Units of analgesics consumed (number of | Standard Deviation 1.2 |
| MD Tissue Collagen Medical Device | Change in Analgesic Drug Consumption (Paracetamol and/or Celecoxib) From Baseline to Week 24 | Week 10 | 0.3 Units of analgesics consumed (number of | Standard Deviation 0.9 |
| MD Tissue Collagen Medical Device | Change in Analgesic Drug Consumption (Paracetamol and/or Celecoxib) From Baseline to Week 24 | Week 24 | 0.7 Units of analgesics consumed (number of | Standard Deviation 2.6 |
Change in Hip Abduction Strength From Baseline to Weeks 6, 10, and 24
Hip abduction strength was assessed using a handheld dynamometer at Weeks 6, 10, and 24. The measurement was performed with the patient standing on the contralateral (healthy) limb, while abducting the hip affected by GTPS. For each assessment, three consecutive measurements were taken and averaged. Results were compared to baseline (Day 0) to evaluate functional improvement in muscular strength.
Time frame: Weeks 6, 10, and 24
Population: All patients who completed dynamometric testing at all timepoints (T0, T6, T10, T24) were included in the per-protocol analysis.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| MD Tissue Collagen Medical Device | Change in Hip Abduction Strength From Baseline to Weeks 6, 10, and 24 | Row Title Number Analyzed Mean SD T0 | 5.538 Force in kg measured by handheld dynamom | Standard Deviation 2.8413 |
| MD Tissue Collagen Medical Device | Change in Hip Abduction Strength From Baseline to Weeks 6, 10, and 24 | T6 | 6.045 Force in kg measured by handheld dynamom | Standard Deviation 2.4797 |
| MD Tissue Collagen Medical Device | Change in Hip Abduction Strength From Baseline to Weeks 6, 10, and 24 | T10w | 6.676 Force in kg measured by handheld dynamom | Standard Deviation 3.0115 |
| MD Tissue Collagen Medical Device | Change in Hip Abduction Strength From Baseline to Weeks 6, 10, and 24 | T24w | 6.851 Force in kg measured by handheld dynamom | Standard Deviation 2.9481 |
Change in Modified Harris Hip Score (mHHS) From Baseline to Weeks 6, 10, and 24
The Modified Harris Hip Score (mHHS) is a validated tool for assessing hip function and pain. It ranges from 0 (worst functional outcome and highest pain) to 100 (best function and least pain). Participants were evaluated at Weeks 6, 10, and 24 compared to baseline. The change in total score is used to assess clinical improvement. Unit of Measure: Score from 0 to 100; higher scores indicate better outcome
Time frame: Weeks 6, 10, and 24
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| MD Tissue Collagen Medical Device | Change in Modified Harris Hip Score (mHHS) From Baseline to Weeks 6, 10, and 24 | T0 (Baseline) | 57.09 Score from 0 to 100; higher scores indic | Standard Deviation 13.78 |
| MD Tissue Collagen Medical Device | Change in Modified Harris Hip Score (mHHS) From Baseline to Weeks 6, 10, and 24 | T6w | 71.22 Score from 0 to 100; higher scores indic | Standard Deviation 11.92 |
| MD Tissue Collagen Medical Device | Change in Modified Harris Hip Score (mHHS) From Baseline to Weeks 6, 10, and 24 | T10w | 72.53 Score from 0 to 100; higher scores indic | Standard Deviation 12.26 |
| MD Tissue Collagen Medical Device | Change in Modified Harris Hip Score (mHHS) From Baseline to Weeks 6, 10, and 24 | T24w | 73.19 Score from 0 to 100; higher scores indic | Standard Deviation 12.74 |
Incidence of Adverse Events (AE, SAE, SUSAR) From Baseline to Week 24
Adverse events (AEs), serious adverse events (SAEs), and suspected unexpected serious adverse reactions (SUSARs) were monitored at each study visit from baseline (Day 0) to Week 24. Data were collected via systematic interviews and clinical assessments. No adverse events of any type were reported during the study. AE definitions followed ICH-GCP and ClinicalTrials.gov guidance.
Time frame: Day 0 to Week 24
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| MD Tissue Collagen Medical Device | Incidence of Adverse Events (AE, SAE, SUSAR) From Baseline to Week 24 | All-Cause Mortality | 0 participants |
| MD Tissue Collagen Medical Device | Incidence of Adverse Events (AE, SAE, SUSAR) From Baseline to Week 24 | Serious Adverse Events | 0 participants |
| MD Tissue Collagen Medical Device | Incidence of Adverse Events (AE, SAE, SUSAR) From Baseline to Week 24 | Other (Non-Serious) Adverse Events | 0 participants |
Mean NRS (Numerical Rating Scale) Pain Score at Week 6 and Week 24 Compared to Baseline (T0)
Pain intensity was measured using the NRS (Numerical Rating Scale) at rest, ranging from 0 (no pain) to 10 (worst possible pain). Participants were asked to rate their pain at baseline (T0), week 6 (T6w/FU), and week 24 (T24w/FU). This outcome reports the mean NRS values at week 6 and 24. Higher scores indicate more intense pain.
Time frame: weeks 6 and weeks 24
Population: All variables were subjected to the appropriate descriptive analyses after validation of the input data. Continuous variables were analyzed as mean ± standard deviation or median and range, depending on the distribution. Categorical variables were summarized as absolute and relative frequency tables.
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| MD Tissue Collagen Medical Device | Mean NRS (Numerical Rating Scale) Pain Score at Week 6 and Week 24 Compared to Baseline (T0) | NRS Week 24 | 2.5 score on a scale |
| MD Tissue Collagen Medical Device | Mean NRS (Numerical Rating Scale) Pain Score at Week 6 and Week 24 Compared to Baseline (T0) | NRS Week 6 | 4.5 score on a scale |
MRI Evaluation of Inflammatory and Degenerative Signs in the Peritrochanteric Region at Week 24 Compared to Baseline
MRI evaluation focused on inflammatory and degenerative signs in the peritrochanteric region (gluteus medius/minimus tendons) was conducted at Week 24 and compared to baseline (Week 0). Two independent radiologists assessed peri-tendinous fluid and intra-tendinous edema on STIR-weighted images. Improvement was defined as visible reduction in peritendinous edema. The analysis was qualitative and dichotomous (Improved vs. Unchanged).
Time frame: Week 24 compared to baseline (Week 0)
Population: Patients who underwent MRI evaluation both at baseline and at Week 24 were included in the analysis (n=40).
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| MD Tissue Collagen Medical Device | MRI Evaluation of Inflammatory and Degenerative Signs in the Peritrochanteric Region at Week 24 Compared to Baseline | 40 Participants with MRI improvement |