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Platelet Rich Fibrin is Compared with Sticky Bone in the evaluation of Post Operative Healing Following Surgical Extraction of Third Molar-A Randomized Control Trail.

To Evaluate the Efficacy of Sticky Bone versus Platelet Rich Fibrin in Promoting Healing Following Surgical Extraction of Mandibular Third Molar-A Randomized Control Trail - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/069712
Enrollment
38
Registered
2024-07-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Health Condition 1: K011- Impacted teeth

Interventions

Intervention1: sticky bone: Only once for 5mins the 20 cc of venous blood will be taken from the cubital vein before the procedure and centrifuged at 2400–2700 rotations per minute (rpm) using a spec

Sponsors

Sharanya Jillapally
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American Society of Anaesthesiologists Grade I patients. (Healthy patients) Patients between the Age group of 21 - 60 years. Patients requiring surgical removal of impacted third molars for prophylactic or therapeutic reasons. Patient willing to participate in the study and willing to come for a review Pederson difficulty index with a tooth score of 5 or less will be included in the study.

Exclusion criteria

Exclusion criteria: Medically compromised patients. The patient is not willing to participate in the study. Patient is allergic to any medications. Acute infections or any carious tooth. Pregnant and lactating mother. Regional malignancy. Individuals under anticoagulant therapy, anemia

Design outcomes

Primary

MeasureTime frame
Pain Trismus Swelling Height of the bony socketTimepoint: Pain at 1st,3rd,7th post operative days Trismus at 1st,3rd,7th post operative days Swelling at 1st,3rd,7th post operative days Height of the bony socket post operatively at preoperative, one month, three months.

Secondary

MeasureTime frame
complicationsTimepoint: post operatively Immediate, one month, six months

Countries

India

Contacts

Public ContactSharanya Jillapally
drjayant27@yahoo.co.in9004799405

Outcome results

None listed

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