Modified 3d Rectangular Grid Plate for Fixation of Anterior and Body Mandibular Fractures
Evaluation of the Use of Modified 3d Rectangular Grid Plate for Fixation of Anterior and Body Mandibular Fractures (Randomized Controlled Clinical Trial)
Background: Fractures of anterior mandible (symphysis and parasymphysis) make up about 9% to 57%, of mandibular fractures, and body fractures make up about 21%; posing challenges for stabilization due to anatomical constraints. Traditional 3D plates have limitations in this area, leading to the development of Modified 3D Rectangular Grid plates. Studies have shown that these plates offer superior stabilization over larger configurations while maintaining a low profile like miniplates. Additionally, design modifications ensure mental nerve preservation, balancing effective fixation with neurovascular safety.
Aim of this study: To evaluate the use of Modified 3D Rectangular Grid plates in comparison with conventional mini plates for fixation of mandibular fracture in the anterior and body regions, clinically regarding pain, interfragmentary mobility, maximal inter-incisal opening, wound healing, and sensory nerve evaluation, and radiographically regrading fracture reduction.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Studietype
Registrering (Faktiske)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiesteder
-
-
Azarita
-
Alexandria, Azarita, Egypt, 00203
- Outpatient Clinic of Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Alexandria University, Egypt
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
Tar imot friske frivillige
Beskrivelse
Inclusion Criteria:
- Patients suffering from recent fractures at the symphysis, parasymphysis and body regions
- Adult patients with no gender predilection who agreed to present for follow-up visits
- A fracture that demands open reduction and internal fixation.
- The patient medically fit for general anesthesia
Exclusion Criteria:
- Patients suffering from recent fractures at the symphysis, parasymphysis and body regions
- Adult patients with no gender predilection who agreed to present for follow-up visits
- A fracture that demands open reduction and internal fixation
- The patient medically fit for general anesthesia
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: 3D plates
|
The system consists of a lower 1.5-mm rectangular plate and an upper linear plate that interlock through circular recesses and elevations.
Each component is 0.75 mm thick at the junction, giving a total thickness of 1.5 mm.
After screw fixation, it provides 3D stability similar to standard 3D plates while minimizing risk to the mental nerve.
|
|
Aktiv komparator: Conventional plates
|
conventional mini plates for fixation of mandibular fracture in the anterior and body regions
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
change in maximum mouth opening
Tidsramme: up to 6 weeks
|
Using a millimetre ruler to measure maximal inter-incisal mouth opening; considered to be adequate if >30 mm and inadequate if <30 mm
|
up to 6 weeks
|
|
change in pain scores
Tidsramme: up to 6 weeks
|
Will be assessed through a 10-point Visual Analogue Scale (VAS).
(0-1= None, 2-4= Mild, 5-7= Moderate, 8-10= Severe
|
up to 6 weeks
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
change in Inter-fragmentary Mobility
Tidsramme: up to 6 weeks
|
The mobility will be assessed by bi-manual palpation across the fracture site.
|
up to 6 weeks
|
|
change in Wound Evaluation
Tidsramme: up to 6 weeks
|
The sutured wounds will be examined for signs and symptoms of infection uisng modified Landry's index
|
up to 6 weeks
|
|
adequacy of fracture line reduction
Tidsramme: 6 weeks
|
Whenever alignment of the inferior border of the mandible will be maintained across the fracture line, it will be considered an excellent reduction.
If a discrepancy of 1-3 mm will be noted, it will be considered a good reduction.
If a discrepancy of 3-5 mm will be noted, it will be labeled as a fair reduction.
If the discrepancy will be > 5 mm, it will be considered a poor reduction.
|
6 weeks
|
Samarbeidspartnere og etterforskere
Sponsor
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
- 1058-04/2025
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. .