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Clinical Trials/NCT04452734
NCT04452734
Completed
Not Applicable

Efficacy of Platelet Rich Plasma (PRP) on Mouth Opening and Pain After Surgical Extraction of Mandibular Third Molars.

Foundation University Islamabad0 sites130 target enrollmentJuly 21, 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Tooth Extraction
Sponsor
Foundation University Islamabad
Enrollment
130
Primary Endpoint
Trismus
Status
Completed
Last Updated
5 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
July 21, 2015
End Date
May 14, 2016
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age between 18-45 iyears
  • Either gender
  • Patients requiring extraction of mandibular 3rd molars
  • 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 -

Exclusion Criteria

  • 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.

Outcomes

Primary Outcomes

Trismus

Time Frame: 7th post op day

Trismus was quantified/measured using Vernier Calliper.

Visual Analogue Scale (VAS)

Time Frame: 7th post op day

Visual Analogue Scale (VAS) used to quantify pain

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