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A Study Comparing Bone Gain After Sinus Lift Surgery Done With And Without Using Low Crystalline Apatite Resorbable Bone Graft Material (LCR) For Dental Implant Placement

Evaluation And Comparison Of Bone Volume Gain After Sinus Floor Augmentation With And Without Using Low Crystalline Apatite Resorbable (LCR) Graft For Placement Of Implant: A Randomized Controlled Trial. - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/104961
Enrollment
30
Registered
2026-02-26
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: K068- Other specified disorders of gingiva and edentulous alveolar ridge

Interventions

Intervention1: Transcrestal hydraulic lift with Low Crystalline Apatite Resorbable (LCR) Graft: Patients will undergo transcrestal hydraulic sinus floor elevation using the CAS kit (Osstem India Pvt.

Sponsors

Dr Maitreyi Limaye
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with minimal residual bone height of greater than or equal to 5mm in maxillary posterior region and patients with adequate alveolar bone width in maxillary posterior region.

Exclusion criteria

Exclusion criteria: Patients having systemic conditions and bone disorders affecting implant surgical treatment outcomes. Patient with sinus pathology such as polyps and mucosal cyst and anatomical constraint like complex septa, aberrant location of PSA neurovascular bundle. Patients with acute and chronic sinusitis, allergic rhinitis and sinusitis or any inflammatory disorders of maxillary sinus. Patients having history of previous sinus surgery. History of radiation to head and neck area. Patients using immunosuppressive agents. Patients who have received antibiotics or anti-inflammatory drugs in the past 3 months. Current and past smokers. Poor oral hygiene. Severe bruxism or clenching.

Design outcomes

Primary

MeasureTime frame
Bone volume gain (vertical bone height) in the augmented sinus regionTimepoint: Baseline (Pre-operative) 6 months post-surgery (RVG assessment) 9 months post-surgery (CBCT assessment)

Secondary

MeasureTime frame
Implant stability and survival rateTimepoint: Immediately post-operative (Primary stability intraoperative torque value) 6 months post-surgery 9 months post-surgery

Countries

India

Contacts

Public ContactDr Maitreyi Limaye

KAHERs KLE VK Institute of Dental Sciences, Belagavi

kumvin@yahoo.com9307349636

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026