Gingival Recession Clinical Trial
Over the years, numerous surgical techniques such as free autografts and pedicle grafts have
been introduced to correct gingival recession defects. Combination grafts with either
autografts or allografts, and newer concepts of guided tissue regeneration (GTR), platelet
concentrates, etc., were developed more recently to correct mucogingival defects. The use of
PRF in various surgical procedures such as degree II furcations, intrabony defects, sinus
floor segmentation during implant placement and on facial plastic surgeries have shown
promising results. However to our knowledge, till this study was completed, no studies have
been reported with the clinical outcomes of autologous platelet rich fibrin membrane for the
treatment of localized gingival recession defects.
Hence, this study was designed to compare coronally advanced flap with platelet rich fibrin
membrane versus subepithelial connective tissue graft in treatment of Miller's Class I and
Class II gingival recession defects.
The study design consist of twenty sites from ten patients were randomly selected by tossing
the coin for the study, which are divided into test group( Root coverage was performed by
coronally advanced flap with platelet rich fibrin membrane) and Control group (Root coverage
was performed with coronal advanced flap with subepithelial connective tissue graft.)
The Surgical Procedure consist of i) Preparation of the recipient bed: After adequate
anesthesia, trapezoidal flap was designed using three incisions which is followed by
reflection of partial thickness flap was raised apical to the crest of the osseous
dehiscence. A periosteal releasing incision was given to enable the coronal advancement of
the flap. Following this, root planing was done and the mesial and distal interdental
papillae were deepithelialized.
The exposed root surface was conditioned with tetracycline hydrochloride for four mins. (The
tetracycline hydrochloride powder was mixed with saline in dappen dish and then applied on
the root surface).
In test group, preparation of PRF was carried out, after which the flap was coronally
positioned over the membrane to completely cover it and secured with non resorbable sutures.
The surgical area was covered with a non - eugenol periodontal dressing with post-operative
antibiotics and analgesics and post-operative instructions that were given to all the
patients.
In control group, connective tissue graft harvesting was carried out which was followed by
placement of connective tissue graft on the recipient site. The connective tissue graft was
placed on the recipient site and secured in position with vicryl sutures. The flap was
coronally positioned over the connective tissue graft and secured with non resorbable
sutures. The recipient bed was covered with a non-eugenol periodontal dressing with
post-operative antibiotics and analgesics and post- operative instructions that were given
to all the patients.
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