Efficacy of Platelet Rich Plasma (PRP) on Mouth Opening and Pain After Surgical Extraction of Mandibular Third Molars.
- Conditions
- Tooth Extraction
- Interventions
- Procedure: Surgical ExtractionProcedure: Platelet Rich Plasma (PRP)
- Registration Number
- NCT04452734
- Lead Sponsor
- Foundation University Islamabad
- Brief Summary
Wisdom tooth extraction is the most common surgical procedure being carried out in oral surgical departments. The complications carried by post operative period include pain and trismus and may affect patient's quality of life.
PRP is an autologous concentrate of platelet in plasma and accelerate healing by production of growth factors. PRP is prepared from patient's own blood and later packed with gel sponge (Spongistone) in the experimental group immediately after surgical extraction of mandibular third molar teeth, followed by suture placement to close the surgical site.
- Detailed Description
Wisdom tooth extraction is the most common surgical procedure being carried out in oral surgical departments. The complications carried by post operative period includes pain, swelling, trismus , along with disturbance in post extraction wound healing which may significantly affect patient's quality of life.
PRP is an autologous concentrate of platelet suspended in plasma and accelerate healing by production of various growth factors. PRP is prepared from patient's own blood and later packed with gel sponge (Spongistone) in the experimental group immediately after surgical extraction of mandibular third molar teeth, followed by suture placement to close the surgical site. PRP speeds up healing by concentration of growth factors which can lessen the inflammation and decreases trismus and pain.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 130
- Age between 18-45 iyears
- Either gender
- Patients requiring extraction of mandibular 3rd molars
- ASA grade1
- Nonsmokers & non alcoholics
- Not allergic to any medicines
- No pain before the extraction procedure
- No trismus, i.e. normal mouth opening before the extraction procedure -
a) Systemic diseases b) Compromised immune system c) Platelet count less than 1.5 lacs/cmm d) Allergy to drugs e) Patients not willing to participate in the study f) Pregnant females/Lactating mothers g) Presence of pericoronitis, periapical infection or any associated lesion.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Control Group Surgical Extraction - Study Group Surgical Extraction - Study Group Platelet Rich Plasma (PRP) -
- Primary Outcome Measures
Name Time Method Trismus 7th post op day Trismus was quantified/measured using Vernier Calliper.
Visual Analogue Scale (VAS) 7th post op day Visual Analogue Scale (VAS) used to quantify pain
- Secondary Outcome Measures
Name Time Method