A Randomized Clinical Study Comparing Xenograft Against Demineralized Freeze-Dried Bone Allograft (DFDBA) in Ridge Preservation for Maxillary Anterior Sites, followed by Implant Placement.
- Conditions
- Health Condition 1: - Health Condition 2: K089- Disorder of teeth and supporting structures, unspecifiedHealth Condition 3: K083- Retained dental root
- Registration Number
- CTRI/2024/05/067479
- Lead Sponsor
- Jwngmashri Basumatary
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1. Subjects of either sex between the age group of 18-16 years, who sign informed consent form for the study.
2. Subjects in whom extraction is indicated in at least one single rooted tooth in anterior maxilla.
3. Clinical root length should be equal to or greater than 8mm.
4. The presence of more than 50% of the buccal bone height.
5.Subjects who is compliant to maintain oral hygiene instructions
6. To select only sites where the tooth location and root angulation is consistent with the ideal implant orientation, where interocclusal distance is adequate for a dental implant placement.
7. Non-smokers.
1. Teeth adjacent to the concerned tooth should not have any periapical or active periodontal disease.
2. Pregnant women or expected pregnancy during the study period.
3. Lactating women.
4. Subjects with bone disease (Paget disease, Rickets, Osteoporosis, Multiple Myeloma etc.) and Radiographic evidence of bone tumour (benign/malignant) or cyst.
5. Subjects under long-term bisphosphonate therapy.
6. Subjects with uncontrolled systemic diseases taking immunosuppressive/ anticoagulant medications.
7. Any medical condition that contraindicates surgery.
8. Any known history of allergy to medications and graft materials used in the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Changes in the bucco-palatal width of the alveolar ridge. <br/ ><br>2. Changes in the vertical height of the alveolar ridge. <br/ ><br>3. Changes in soft tissue (width and thickness of keratinised gingiva).Timepoint: 1. Baseline <br/ ><br>2. 6months
- Secondary Outcome Measures
Name Time Method 1.To assess the clinical adverse effects of the grafts, if any. <br/ ><br>2.Changes in clinical attachment level (CAL) at teeth adjacent to the extraction siteTimepoint: 1. Baseline <br/ ><br>2. 6months