Skip to content

A Clinical Trial to study the healing of extraction socket and implant stability on using a naturally sourced bone graft

Evaluation of healing of extraction socket, bone morphologic changes, primary implant stability and patient reported outcome measures with the use of E-Bone (naturally sourced nano-hydroxyapatite graft): A Randomized Control Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/07/044401
Enrollment
26
Registered
2022-07-27
Start date
Unknown
Completion date
Unknown
Last updated
2022-08-02

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

Conditions

Health Condition 1: K080- Exfoliation of teeth due to systemic causes Health Condition 2: K088- Other specified disorders of teethand supporting structures Health Condition 3: K083- Retained dental root Health Condition 4: K085- Unsatisfactory restoration of tooth

Interventions

Intervention1: Egg shell derived nano hydoxyapatite biomaterial: Dose-as needed to fill the defect approximately 1gm for socket to fill in molar and 0.5gm for other teeth Duration- One time implantati

Sponsors

Mahatma Gandhi Dental College and Hospital
Lead Sponsor
Dr Girija EK
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients who had teeth with indication for extraction, with extensive cavities, root fracture or vertical periodontal defects of maxillary or mandibular first and second molars.2. Patients in whom single or multiple teeth were indicated for extraction for reasons other than chronic periodontitis.3. Patients with age 18-45 years with good oral hygiene and teeth in need of extraction in regions where the use of a temporary prosthesis or mucosal support was not necessary shall be recruited.

Exclusion criteria

Exclusion criteria: 1. Smokers, ASA III and IV, pregnant women, patients with Stage III or IV periodontal disease will be excluded from the study. 2. Patients with gross tooth mobility due to complete bone loss (more than 3/4 of root length). 3. Patients with any abnormal findings during clinical or radiological examination. Example: Patients with ankylosed roots or other root morphological alterations that may complicate the procedure. 4. Patients undergoing Immunosuppressive conditions such as AIDS, Cancer or Radiation therapies. 5. Subjects with positive COVID results.

Design outcomes

Primary

MeasureTime frame
Assessment of the bone quality and bone dimensions and assessment of primary stability of implantTimepoint: 4 months after tooth extraction surgery

Secondary

MeasureTime frame
Histomorphic EvaluationTimepoint: At time of implant placement (4 months after tooth extraction surgery);Number of consultationTimepoint: At time of implant placement (4 months after tooth extraction surgery);PainTimepoint: At time of implant placement (4 months after tooth extraction surgery);Recommendation of patientTimepoint: At time of implant placement (4 months after tooth extraction surgery);Treatment difficultyTimepoint: At time of implant placement (4 months after tooth extraction surgery)

Countries

India

Contacts

Public ContactDr Pragati Kaurani

Sibar Institute of Dental Sciences

drvivekanandsk@gmail.com9492473628

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026