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"Assessing the Effectiveness of bio-material in Improving Implant Stability and Bone Health: A Clinical Study"

Evaluating the efficacy of application of i-prf on implant stability and marginal bone levels: A randomized clinical study - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/077058
Enrollment
30
Registered
2024-11-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: - Health Condition 2: K084- Partial loss of teeth Health Condition 3: K084- Partial loss of teeth

Interventions

Intervention1: Implant placement with Injectable Platelet Rich Fibrin: 15 sites will be selected based on inclusion criteria and Injectable Platelet Rich Fibrin applied slowly over the implant surface

Sponsors

Jyothi Prasanna Paritala
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: i)Systemically healthy patients(ASA I,II). ii)Patients with Stable occlusion. iii)Adequate bone height and width at the surgical site. iv)Adequate mesiodistal and interocclusal spaces in the edentulous area.

Exclusion criteria

Exclusion criteria: ?Presence of active periodontal disease. ?Pregnancy or Lactation women. i)Patients with any systemic disease and medications that will interfere with treatment outcome. ii)History of radiotherapy or chemotherapy. iii)Primary stability less than 25 Ncm during fixture placement.

Design outcomes

Primary

MeasureTime frame
Implant stability measurement, Radiographic evaluationTimepoint: Baseline,10 days,1 month, 3 months and 6 months

Secondary

MeasureTime frame
Radiographic evaluationTimepoint: 3 months and 6 months

Countries

India

Contacts

Public ContactDr.Jyothi Prasanna Paritala

GSL Dental College and Hospital

anu3267@gmail.com9985313267

Outcome results

None listed

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