Skip to content

COMPARE THE SOFT TISSUE AND BONE LEVELS AROUND DENTAL IMPLANTS PLACED IN IMMEDIATE AND DELAYED TOOTH EXTRACTION SOCKETS

CLINICO-RADIOGRAPHIC EVALUATION OF PERI-IMPLANT SOFT TISSUES AND HARD TISSUES IN TITANIUM IMPLANTS IN IMMEDIATE AND DELAYED CASES: A COMPARATIVE PROSPECTIVE STUDY

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/06/025873
Enrollment
40
Registered
2020-06-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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 Health Condition 2: K069- Disorder of gingiva and edentulousalveolar ridge, unspecified

Interventions

Intervention1: Aktiv grade 5 titanium dental implants: In immediate extraction sockets, Aktiv grade 5 titanium dental implants will be placed. Control Intervention1: Aktiv grade 5 titanium dental impl

Sponsors

SCB DENTAL COLLEGE AND HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Fresh extraction sockets of maxillary teeth in the esthetic zone (experimental group) and healed extraction sites in esthetic zone of maxilla (control group- atleast 6 months elapsed after tooth loss) 2.Age ( >18 years) 3.Sufficient alveolar bone height and width 4.Patient willing to and fully capable of complying with the study protocol

Exclusion criteria

Exclusion criteria: 1.Patients with systemic co-morbidities (uncontrolled diabetes mellitus, immunocompromised patient, psychological problems, radiotherapy to head and neck region within past 24 months etc.) 2.Severe periodontal problem 3.Chronic alcoholism, smoking 4.When bone or soft tissue regeneration is needed to enhance implant stability or esthetics 5.Soft and hard tissue defect that could impair the esthetic outcome of the treated site 6.Patient under medications which are likely to affect the treatment outcome

Design outcomes

Primary

MeasureTime frame
Peri-implant soft tissue clinical measurements Timepoint: 1 WEEK, 1 MONTH, 3 MONTH, 6 MONTH

Secondary

MeasureTime frame
Peri-implant crestal bone loss( in mm)Timepoint: 6 months

Countries

India

Contacts

Public ContactDEBAJANI BARAL

S.C.B. DENTAL COLLEGE AND HOSPITAL

drsubash007@gmail.com9437008298

Outcome results

None listed

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