Sinus Lift Using PTFE Titanium Reinforced Membrane

Evaluation of Direct Sinus Lift Using Ptfe Titanium Reinfored Membrane Assosiated With Immediate Implant Placement (Clinical Trial)

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT05044260

Enrollment

Registered

2021-09-14

Start date

2020-09-01

Completion date

2021-10-20

Last updated

2021-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sinus Lift

Brief summary

Various attempts have been implemented using different materials and techniques to augment the maxillary sinus floor enhancing autogenous bone formation to allow proper dental implant positioning. The aim of this study is to evaluate the sinus lift procedure using polytetrafluoroethylene (PTFE) titanium-reinforced membrane to maintain the space formed after Schneiderian membrane elevation followed by immediate implant placement.

Interventions

PROCEDUREDirect sinus lift with titanium reinforced PTFE membrane

Implants will be placed immediately after sinus lifting procedure and maintaining the sinus membrane in position using PTFE titanium reinforced membrane.

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

40 Years to 60 Years

Healthy volunteers

Inclusion criteria

* Patients of both genders requiring implant placement in posterior maxilla * Age range: 40-60 years. * Good oral hygiene * Healthy maxillary sinus free from pathology * The minimum crestal bone height is (4-6) mm * Patients who are willing and fully capable to comply with the study protocol.

Exclusion criteria

* Sinus infection * Tumors or pathologic lesions in sinus * Severe allergic rhinitis. * Chronic topical steroid use. * Radiation therapy. * Psychologic / mental impairment * Acute infection (periodontitis or mucosal infection * Patients on radiotherapy or chemotherapy. * Alcohol or drug abuse. * Patient with systemic disorder (uncontrolled Diabetes mellitus, autoimmune diseases, bone diseases, etc.) * Smokers * Parafuctional habits

Design outcomes

Primary

Measure	Time frame	Description
Change in implant stability	at baseline and 6 months	It will be measured using Osstell
Change in bone formation	at baseline and 6 months	It will be measured uisng CBCT on Demand 3d software
Change in bone height	at baseline and 6 months	It will be measured uisng CBCT on Demand 3d software
Change in bone density	at baseline and 6 months	It will be measured uisng CBCT on Demand 3d software

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026