To check whether the dental implant placed in the upper back teeth region is strong after placing with different material

Comparative evaluation of the effects of injectable-platelet rich fibrin (I-PRF) and synthetic graft on the implant stability following indirect sinus augmentation - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/03/081640

Enrollment

Registered

2025-03-04

Start date

Unknown

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

Health Condition 1: K069- Disorder of gingiva and edentulousalveolar ridge, unspecified

Interventions

Intervention1: Indirect Sinus Augmentation: Indirect Sinus Augmentation using Injectable Platelet Rich Fibrin (I-PRF), Synthetic Graft and without Graft Total duration 6 months Control Intervention1:

Eligibility

Inclusion criteria

Inclusion criteria: Participants will be selected using the following criteria: 1. Healed edentulous ridge in the maxillary pre-molar or molar region. 2. Residual bone height ranging from 4 to 6 mm. 3. Crestal bone width ranging from 6 to 8 mm. 4. Maintaining Good oral hygiene

Exclusion criteria

Exclusion criteria: 1. Systemic conditions such as uncontrolled diabetes mellitus, hypertension and bleeding disorder 2. Presence of active sinusitis 3. Sinus membrane thickening of more than 2mm 4. Patients on long term steroid therapy or bisphosphonate medication 5. Any previous history of sinus surgery 6. Untreated active periodontitis in neighbouring teeth 7. Participants who are current smokers 8. Pregnant women and nursing mothers

Design outcomes

Primary

Measure	Time frame
To assess the implant stability following indirect sinus augmentation using Injectable-Platelet Rich Fibrin (I-PRF), synthetic graft and without graftTimepoint: at baseleine, at 6 months after implant placement	—

Secondary

Measure	Time frame
To compare the stability of the implant following indirect sinus augmentation using Injectable-Platelet Rich Fibrin (I-PRF), synthetic graft & without bone graft.Timepoint: At baseline & after 6 months after implant placement	—

Countries

India

Contacts

Public ContactDr Sunaina M

Yenepoya Dental College

ragher@yenepoya.edu.in7676708707

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Apr 2, 2026