Graftless Lateral Sinus Lifting Using Peizo Electric Device in Patients With Atrophic Maxilla
Guided Versus Conventional Graftless Lateral Sinus Lifting Using Peizo Electric Device in Patients With Atrophic Maxilla [a Randomized Controlled Clinical Trial]
Background: Dental implant therapy in the posterior maxilla may be difficult owing to limited bone height after dental extraction with sinus pneumatization. Several approaches for sinus floor elevation have been documented, and hence lateral sinus lifting using surgical guide is used.
Aim of the study: To compare between guided and conventional sinus lifting using piezoelectric device in patients with atrophic maxilla.
Methods: This study will be carried out as a randomized controlled clinical trial; patients will be randomly allocated into two groups: in the study group 15 patients will undergo lateral sinus lifting using surgical guide, while in the control group 15 patients will undergo conventional sinus lifting without surgical guide with simultaneous implant placement.
Clinical evaluation including intraoperative assessment of duration of surgery and immediate complications such as perforation of Schneiderian membrane, arterial laceration and trauma to adjacent roots and nasal bleeding. Primary implant stability will be measured immediately after implant placement
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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Azarita
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Alexandria, Azarita, Egypten, 00203
- Outpatient Clinic of Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Alexandria University, Egypt
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- Patient seeking replacement of a missed maxillary posterior tooth/ teeth by a delayed dental implant procedure
- Residual bone height is 4-5 mm measured from crestal bone to sinus floor.
- Both genders.
- Good oral hygiene
Exclusion Criteria:
- Recent radiation therapy in maxilla.
- Uncontrolled systemic diseases such as diabetes mellitus.
- Acute/chronic maxillary sinusitis.
- Heavy smoker (those who smoke ≥ 25 cigarettes a day).
- Alcohol abuse.
- Psychosis.
- Severe allergic rhinitis.
- Tumor or large cyst in the maxillary sinus.
- Oroantral fistula.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Aktiv komparator: Kontrolgruppe
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including 15 patients who will be treated by conventional lateral sinus lifting without using a surgical guide with simultaneous implant placement.
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Eksperimentel: Testgruppe
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Including 15 patients who will be treated by lateral sinus lifting using a surgical guide with simultaneous implant placement.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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implant stability
Tidsramme: 6 months
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• Secondary implant stability will be measured 6 months post-operatively using Osstell device.
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6 months
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change in pain scores
Tidsramme: up to 7 days
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- Post operative pain will be assessed through a 10 point visual analogue scale (VAS).
(0-1=none, 2-4=mild, 5-7=moderate, 8-10=severe)
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up to 7 days
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Post operative edema
Tidsramme: 1 week
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it will be assessed in the 1st week as following:
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1 week
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Samarbejdspartnere og efterforskere
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- 1073-5/2026
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