Maxillary Sinus Lifting: A Comparison Of Success Rate of Direct Versus Indirect Sinus Lifting for Vertical Bone Augmentation in Patients Receiving Dental Implants

Not Applicable

• Conditions: Missing tooth.; Complete loss of teeth; K08.1

• Registration Number: IRCT20230926059527N2
• Lead Sponsor: AFID

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 16 October 2023

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

Having physical status 1 according to ASA classification
HaviBone Height Less than 5mm in Maxillary Molar Region

Exclusion Criteria

Pregnant women, nursing mothers & smokers
Patient with infection in Maxillary Molar Region
Patients Having Sinus Pathology
Patient with medications that can alter pain perception

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Post Op Pain. Timepoint: 3rd and 5th Day after Intervention. Method of measurement: Visual Analogue Scale.;Gingival inflammation. Timepoint: 3rd and 5th Day after Intervention. Method of measurement: Gingival Index.;Swelling. Timepoint: 3rd and 5th Day after Intervention. Method of measurement: Observed Clinically.;Implant Stability. Timepoint: 03 Months after Intervention. Method of measurement: Glickemans method.;Per Op patient Compliance. Timepoint: immediately after intervention. Method of measurement: Licekrts Scale.