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Platelet Rich Fibrin VS Hyaloronic Acid in Management of Pain After Harvesting a Free Gingival Graft

Clinical Comparison of Platelet Rich Fibrin Versus Topical Application of Hyaluronic-Acid Gel in Management of Pain And Wound Healing After Free Gingival Graft Harvesting: A Randomized Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03814707
Enrollment
26
Registered
2019-01-24
Start date
2019-01-10
Completion date
2019-07-31
Last updated
2019-01-28

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

Conditions

Pain, Postoperative

Keywords

gingival recession, gingival augmentation, free gingival graft, platelet rich fibrin in wound healing, 2 steps free gingival graft, hyaluronic acid in wound healing

Brief summary

Comparative study to assess the efficacy of topical application of 0.2% hyaluronic acid vs platelet rich fibrin in decreasing a postoperative pain following free gingival graft procedure . .

Detailed description

\- Patients of both groups will be subjected to: 1. Case history including personal data, medical, surgical history and family history. 2. Clinical Examination. After local infiltration of anesthesia, an adequate size of supraperiosteal recipient bed was prepared to receive the palatal graft of 15 mm mesio-distal width with 8 mm apico-coronal extension.. The free gingival graft extended from the mesial line angle upper 5 and distal line angle of upper 6 . The coronal horizontal incision, will be 15 mm long, at least 2 mm apical from the gingival margin. A second horizontal incision will be drawn 8 mm apico coronal . Care will be taken to obtain a graft thickness of 1.5 mm. Thickness will be measured at the central point of the graft during the surgery by using an endodontic file then the grafts will be positioned, and firmly adapted to the bed, and stabilized with simple periosteal sutures. Preparation of platelet rich fibrin:( intervention group) The classic PRF protocol was introduced by Choukroun & coworkers. PRF requires around 10 ml of blood to be collected from the forearm of patient without anticoagulant in a glass coated plastic tubes. After collection, the blood will be quickly subjected to centrifugation at 2700-3000 rpm for 12 minutes. After the completion of cycle, the blood become separated into three distinct layers; platelet poor plasma at the top, PRF in the middle and a red blood corpuscular base in the bottom. Pliers will be inserted into the tube to gently grab the fibrin clot with attached RBC's. The clot thus obtained will be compressed to form plugs to be placed in the palatal donor site and stabilized by criss cross resorbable suture then covered by periodontal pack control group Control group: As the intervention group but the palatal wound will receive a .2% hyaluronic acid gel then covered by periodontal dressing ..

Interventions

DRUGTopical application of 0.2% hyaluronic acid gel

Topical application of 0.2% hyaluronic acid gel will be placed immediately in palatal donor site after free gingival graft harvesting

BIOLOGICALPlatelet rich fibrin

Placement of Platelet rich fibrin in the palatal donor sie after free gingival graft harvesting and suturing by criss cross sutured then covered by periodontal pack.

Sponsors

Cairo University
CollaboratorOTHER
mostafa soliman
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

both the participants and the investigator can't be blinded only outcome assessor will be blinded .

Intervention model description

Parallel Assignment * A randomized clinical trial. * Parallel group study. * A trial will be carried out in department of periodontology - Faculty of Oral and Dental medicine - Cairo University . * Equal randomization : participants with equal probabilities for intervention. * Positive controlled : Both groups receiving treatment.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

for participants: * Patients with mucogingival defects scheduled for free gingival graft * Age at least 18 years. * Not having any systemic disease that could compromise wound healing * No previous periodontal surgery on the experimental sites.

Exclusion criteria

for participants: * Systemic diseases that may be a contraindication for any surgeries. * Loss of maxillary premolars and molars. * Pregnancy or lactation * Smoking

Design outcomes

Primary

MeasureTime frameDescription
post operative pain1 weekQuestionnaire will be used to evaluate the postoperative pain using visual analogue scale ( VAS) Min score Zero , Max score ten where zero is the best while ten is the worst

Secondary

MeasureTime frameDescription
wound healing2 monthsEarly Wound Healing Index (EHI) , measuring unit Binary (YES/NO)

Countries

Egypt

Contacts

Primary ContactMostafa M Soliman, B.D.S
drshoo_2010@hotmail.com002-01007034062
Backup ContactMona M Shoeib, P.H.D
monashoeib@gmail.com002-01223102216

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026