Hydrodynamic sinus lift procedures in periodontally compromised teeth with Immediate Implant Placement.

Phase 2

Completed

• Conditions: Health Condition 1: K069- Disorder of gingiva and edentulousalveolar ridge, unspecifiedHealth Condition 2: K069- Disorder of gingiva and edentulousalveolar ridge, unspecified

• Registration Number: CTRI/2020/03/023771
• Lead Sponsor: J Arockia Antony Praveen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2021-11-11
• Last Update Posted: 17 October 2022

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 26

Inclusion Criteria

1.The participant must be more than 18 years of age and lesser than 65 years.

2.Patients who are systemically healthy; with no disease that will have a bearing on the outcome of the surgical intervention.

3.Isolated teeth in the posterior maxilla with advanced bone loss due to periodontal disease in posterior maxillary region extending up to the apical 3rd of the root, with native bone of 3 to 5 mm apical to the root apex.

4.Teeth with endo-perio lesion in the posterior maxilla that is indicated for extraction, with bone dimensions as in the previous criterion.

5.Fresh extraction sockets which has a minimum of 3mm apico-coronal dimension of socket walls, along all the roots, following extraction of teeth that fulfil the previous criterion.

6.Current smoker will not be included in this study.

Exclusion Criteria

1.Patients with uncontrolled systemic disease or drugs that contraindicates periodontal surgery.

2. Patients with septa at the level of the sinus lift.

3. Pregnant and lactating women.

4. Participants with rhinitis, sinusitis, and maxillary pathology will be excluded from the study.

5. Participants must not have previous implant treatment or bone grafting in the targeted site.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1.The incidence of sinus membrane perforations. <br/ ><br>2.The incidence of nasal bleeding. <br/ ><br>3.The incidence of post-operative maxillary sinusitis <br/ ><br>Timepoint: During and After the surgical procedure and at the first week post surgery. <br/ ><br>

Secondary Outcome Measures

Name	Time	Method
1.Primary Implant stability. <br/ ><br>2.Secondary Implant stability. <br/ ><br>3.Crestal Bone levels assessed at baseline and at 6 months of implant placement, to as assess Crestal Bone Remodelling by standardized intra-oral periapical radiographs <br/ ><br>Timepoint: After the surgical procedure and at the end of six months.