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Comparing the Benefits of T-PRF with and without Laser for Dental Implants in the Back of the Lower Jaw: A Randomized Study

Assessment of the Bio-Stimulatory Impact of T-PRF compared to T-PRF Augmented with Diode Laser in Dental Implants for the Replacement of Posterior Mandibular Teeth: A Randomized Control Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072935
Enrollment
22
Registered
2024-08-22
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: K081- Complete loss of teeth

Interventions

Intervention1: Low level Laser Diode and T PRF: LLLT will be performed using Diode Laser, with Red wavelength- 660nm wavelength for Photobiomodulation. The Laser operating mode will be Continuous wave

Sponsors

Shwetank Dwivedi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Bilateral absence of teeth in the posterior mandibular region Lack of any pathology at the time of the interference in the posterior area Patient expressing voluntary willingness to participate and having signed informed consent for the described procedure Patient exhibiting good physical and mental health with a well-formed/ moderate residual alveolar ridge Patients well motivated for implant therapy and maintain good oral hygiene

Exclusion criteria

Exclusion criteria: Systemic diseases including metabolic bone disorders uncontrolled diabetes mellitus autoimmune disorders Recent corticosteroid use Infectious diseases Allergies to materials or medications employed in trial Psychological disorders like parafunctional habits and bruxism Presence of a slender ridge Bad oral health Pregnancy Chronic smokers Individuals engaged in alcohol or drug abuse

Design outcomes

Primary

MeasureTime frame
Assessment of Postoperative Pain Assessment of Implant Stability Assessment of Bone DensityTimepoint: Postoperative Pain 2 4 7 10 14 Days Implant Stability Immediately 3 6 months Bone Density Preoperative 3 months

Secondary

MeasureTime frame
nilTimepoint: nil

Countries

India

Contacts

Public ContactShwetank Dwivedi

Sardar Patel Post Graduate Institute of Dental and Medical Sciences

drlovebhatia12@gmail.com9451833111

Outcome results

None listed

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