Actively Recruiting

Phase 4
Age: 18Years +
All Genders
NCT07459075

Radiographical, Histomorphometrical and Biomarker Analysis After Maxillary Sinus Augmentation Utilizing Xenograft Particulate Bone Graft Mixed With Parathyroid Hormone

Led by University of Baghdad · Updated on 2026-03-09

30

Participants Needed

1

Research Sites

78 weeks

Total Duration

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AI-Summary

What this Trial Is About

This study aimed the to investigate the beneficial effect of combining PTH with bovine-derived bone graft bone in maxillary sinus augmentation. There is limited information available about the effect of PTH on maxillary sinus augmentation to achieve a clear understanding of PTH's efficacy in bone regeneration and bone remodelling through radiological, clinical, biomarker, histological and histomorphometric assessment . Objectives 1. Evaluation of the bone density at the planned implants sites using cone beam computed tomography (CBCT). 2. Histomorphometry examination of maxillary sinus bone to measure (bone trabeculae, connective tissue, osteoblast, osteocyte) after healing 4 months after augmentation. 3. Osteopontin as biomarker analysis for bone regeneration and osteoblast activity. 4. Evaluate the primary stability of implant in upper posterior area filled with PTH (1 34) and bovine-derived bone graft compared to bovine-derived bone graft alone.

CONDITIONS

Official Title

Radiographical, Histomorphometrical and Biomarker Analysis After Maxillary Sinus Augmentation Utilizing Xenograft Particulate Bone Graft Mixed With Parathyroid Hormone

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy individuals without systemic disease or local sinus lesions affecting bone healing
  • Fair to good oral hygiene
  • Age 18 years or older
  • Residual bone height (RBH) of 3 mm or less in the posterior maxillary ridge
  • Adequate ridge width of 5 mm or more to support implant stability
  • Healed planned implant insertion site
Not Eligible

You will not qualify if you...

  • Medical conditions interfering with healing or osseointegration, including uncontrolled diabetes, chemotherapy, corticosteroids, bisphosphonates, recent head and neck radiotherapy, bleeding disorders, pregnancy, thyroid hormone issues, or psychiatric disorders
  • Residual bone height greater than 3 mm
  • Sinus membrane thickness greater than 5 mm
  • Acute or chronic maxillary sinusitis or other sinus pathologies
  • Previous maxillary sinus surgery
  • Heavy smoking of 20 or more cigarettes daily or alcohol abuse
  • Severe bruxism or clenching (parafunctional habits)

AI-Screening

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Trial Site Locations

Total: 1 location

1

Baghdad University

Baghdad, Iraq

Actively Recruiting

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Research Team

M

Mohanad Ali Ali Shabat, Msc,PhD student in Oral surgey

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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