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A comparative study on combined use of platelet rich plasma and diode laser with Piezosurgery device versus xenograft with conventional rotary surgery in improving reparative osteogenesis in benign cyst like lesions causing bony defect

a comparative study on combined use of platelet rich plasma and diode laser with piezosurgery device versus xenograft with conventional rotary surgery in improving reparative osteogenesis in benign cyst like lesions causing bony defect - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112458
Enrollment
10
Registered
2026-06-10
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

None listed

Interventions

Intervention1: Platelet Rich Plasma And Diode Laser Assisted Piezosurgery With Xenograft: enucleation of benign cystic lesion followed by piezosurgery assisted osteotomy. platelet rich plasma and diod

Sponsors

Self
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Bone defects that were formed of diameter not exceeding 2 cm. Patients who have not undergone any surgical or medicinal treatment for the same before. Patients who are willing to participate in the study. Patients who are ready to attend regular follow ups for at least 6 months.

Exclusion criteria

Exclusion criteria: Pregnant or lactating women. Patients who have any drug allergy. Patients with Bleeding disorders. Medically compromised patients Patients with clinical signs and symptoms or proven report of other malignancy in oral cavity Patients who declined to participate in study

Design outcomes

Primary

MeasureTime frame
Assessment of reparative osteogenesis and bone healing in benign cyst like lesions treated with PRP and diode laser and piezosurgery device versus xenograft with conventional rotatory surgeryTimepoint: One-time surgical intervention 1 to 2 hours with followed up at 1st 3rd and 6th months so 6 months

Secondary

MeasureTime frame
post operative pain assessment using visual analog scale (VAS).Assessment of swelling and infection. Radiographic assessment of bone density.Timepoint: 1st day,3rd day, 7th day postoperatively.3rd and 7th day postoperatively.3months and 6 months follow up.

Countries

India

Contacts

Public ContactChetna Kori

Hitkarini Dental College And Hospital

asranisumit@gmail.com9827368458

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026