Triple-Modal Therapy in Early-Stage Femoral Head Osteonecrosis (TM-ONFH) (TM-ONFH)
Triple-Modal Therapy (Core Decompression, Stromal Vascular Fraction, and Hyperbaric Oxygen Therapy) is Associated Improved Clinical and Radiologic Outcomes in Early-Stage Osteonecrosis of the Femoral Head: Two-Year Follow-Up of 24 Patients
Studieoversikt
Status
Forhold
Detaljert beskrivelse
Osteonecrosis of the femoral head (ONFH) is a progressive disease that can lead to femoral head collapse and the need for total hip arthroplasty. Joint-preserving treatments are particularly important in early-stage disease. Core decompression is a widely used technique to reduce intraosseous pressure and improve blood flow. Stromal vascular fraction (SVF), which contains mesenchymal stem cells, may enhance bone regeneration. Hyperbaric oxygen therapy (HBOT) has been shown to improve tissue oxygenation and promote healing.
In this study, patients with early-stage ONFH who underwent a combined treatment of core decompression, SVF injection, and HBOT were retrospectively analyzed. Clinical outcomes were assessed using functional scores, and radiological progression was evaluated during a two-year follow-up period. The purpose of this study is to determine whether this triple-modal therapy provides improved outcomes compared to conventional treatment approaches.
Studietype
Registrering (Faktiske)
Kontakter og plasseringer
Studiesteder
-
-
-
Ankara, Tyrkia (Türkiye), 06800
- Ankara Bilkent City Hospital
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Prøvetakingsmetode
Studiepopulasjon
Beskrivelse
Inclusion Criteria:
- Patients diagnosed with Ficat-Arlet Stage II osteonecrosis of the femoral head
- Patients treated with combined core decompression, stromal vascular fraction (SVF), and hyperbaric oxygen therapy (HBOT)
- Age between 18 and 65 years
- Patients who completed all components of the treatment protocol
- Minimum follow-up duration of 24 months
Exclusion Criteria:
- Patients with advanced-stage osteonecrosis (Ficat-Arlet Stage III-IV)
- Patients with a history of previous hip surgery
- Patients who previously received hyperbaric oxygen therapy for ONFH
- Patients who received prior cellular therapies (e.g., stem cell therapy or PRP) in the hip joint
- Patients with incomplete medical records
- Patients who did not complete the full treatment protocol
- Patients with follow-up duration less than 24 months
Studieplan
Hvordan er studiet utformet?
Designdetaljer
Kohorter og intervensjoner
Gruppe / Kohort |
Intervensjon / Behandling |
|---|---|
|
Triple-Modal Therapy Group
Patients with early-stage osteonecrosis of the femoral head treated with a combination of core decompression, stromal vascular fraction (SVF), and hyperbaric oxygen therapy (HBOT).
|
Surgical procedure performed to reduce intraosseous pressure and improve blood flow in the femoral head.
Autologous stromal vascular fraction containing mesenchymal stem cells applied to enhance bone regeneration.
Adjunctive hyperbaric oxygen therapy used to improve tissue oxygenation and promote healing.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in Modified Harris Hip Score (MHHS)
Tidsramme: Baseline to 24 months
|
Assessment of clinical improvement using the Modifed Harris Hip Score in patients treated with triple-modal therapy.
|
Baseline to 24 months
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Radiological progression of osteonecrosis
Tidsramme: Baseline to 24 months
|
Evaluation of disease progression using radiographic imaging.
|
Baseline to 24 months
|
|
Conversion to total hip arthroplasty (THA)
Tidsramme: 24 months
|
Number of patients requiring total hip arthroplasty during follow-up.
|
24 months
|
Samarbeidspartnere og etterforskere
Sponsor
Etterforskere
- Studiestol: ibrahim alper yavuz, MD, PhD, Ankara Bilkent City Hospital, Department of Orthopedics and Traumatology
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- TABED 2-25-843
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .