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Improving dental implant life

Biological and esthetic outcome of immediate dental implant after photofunctionalization or use of Platelet rich growth factors: a Randomized controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/06/014562
Enrollment
39
Registered
2018-06-18
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Health Condition 1: null- Maxillary or mandibular anterior missing teeth

Interventions

Intervention1: photofunctionalized dental implant: Participants in this group will be given standard root form implant after photofunctionalization during implant placement in single maxillary or mand

Sponsors

King Georges Medical University Lucknow
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Male and female of 18-60 years and willing to pay implant cost by themselves. 2. Ability to understand and provide informed consent before starting the study. 3. Adequate oral hygiene to allow for implant therapy consistent with standards of care. 4. Adequate bone volume to accommodate the planned endosseous dental implant placement following immediate placement protocols. 5. One tooth in either the maxilla or mandible anterior area requiring extraction leading to a single-tooth gap. 6. Following extraction, surgical site anatomy presents conditions allowing immediate implant placement.

Exclusion criteria

Exclusion criteria: 1. Current smoking habit with moderate or heavy smoking (more than 10 cigarettes per day) or tobacco chewing use. 2. History of alcoholism or drug abuse within the past 5 years. 3. Severe bruxism or clenching habits. 4. Patient has significant untreated periodontal disease (grade III or IV), caries, or clinical or radiographic signs of infection within two adjacent tooth positions of implant area. 5. Patients with a history of systemic disease that precludes standard dental implant therapy. 6. Patient currently undergoing chemotherapy/radiotherapy or drugs that interfere with the study. 7. Extraction sites having anatomic conditions that preclude immediate implant placement.

Design outcomes

Primary

MeasureTime frame
Implant stability by Resonance Frequency analyzerTimepoint: Implant stability

Secondary

MeasureTime frame
Esthetic outcome by Pink and White esthetic scoreTimepoint: 1, 3, 6, and 12 months;Marginal bone loss by digital Intraoral Periapical View using standardized radiographic stentTimepoint: 1, 3, 6, 12 months;Success rate by Smith and Zarbs criteriaTimepoint: 6 months

Countries

India

Contacts

Public ContactBalendra Pratap Singh

King Georges Medical University, Lucknow

balendra02@yahoo.com9839121151

Outcome results

None listed

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