Track topics on Twitter Track topics that are important to you
Cyanoacrylate tissue adhesives have been successfully used for wound closure. The purpose of this clinical trial is to compare cyanoacrylate tissue adhesives to polytetrafluoroethylene (PTFE) sutures in the donor site of connective tissue grafts. Two groups of volunteers will randomly assigned to one of the two study groups. The wound closure at the palatal donor area will be achieved with polytetrafluoroethylene (PTFE) sutures in one group and with high viscosity cyanoacrylate tissue adhesives on the other group. The surgical procedure will be performed by one of three calibrated periodontics residents. Data will be collected at baseline-day of the surgery and in one week post-operatively. The primary outcome is patient's discomfort from the donor site during the first week after the surgery. Secondary outcomes is the time required for suture placement or cyanoacrylate application, patient's pain from donor and recipient site one week post-operatively, painkillers intake, presence or absence of inflammation and modified EHI early-wound healing index.
A prospective, randomized clinical trial will be conducted to determine whether cyanoacrylate tissue adhesives or sutures are better tolerated by patients receiving soft tissue gum grafts.
Periodontal plastic surgery procedures have become an integral part of periodontal treatment by addressing esthetic and functional demands. Several therapeutic modalities such as free gingival graft , pedicle flaps , connective tissue grafts , grafts combining the two lateral modalities  and guided tissue regeneration  have been used for covering the denuded roots and augmenting the width and thickness of the keratinized gingiva . Among various surgical techniques, subepithelial connective tissue (SECT) grafts remain the most commonly used and most successful root coverage procedures . The esthetic and functional success of SECT graft techniques is highly predictable and reliable and they have given them a common place in the clinical practice . Subepithelial connective tissue graft procedures require harvesting tissue from a donor area, usually the palate . This addition of another surgical site extends the complexity of the procedure and increases patient discomfort .
Single interrupted  or continuous interlocking  sutures are suggested at the donor site. Suturing is the most common method of wound closure. Other biomaterials such as staples, adhesive tapes, adhesive glues and fibrin sealants have been used generally to hasten the pace of healing . Adhesives interact with different materials, merge and allow them to remain whole . Cyanoacrylates are bio-adhesives that were discovered by Ardis in 1949 and first used for surgery by Coover et al in 1959    . When applied to two opposing, wet, living tissue surfaces, they have the ability to cement them in place  . Their general chemical formula is CH2=C(CN)-COOR , where R can be substituted for any alkyl group, ranging from methyl to decyl    . They polymerize rapidly within seconds in an exothermic reaction following contact with proteinaceous surfaces to form strong and flexible bonds . Methyl cyanoacrylate was the first glue developed, but tissue toxicity precluded its use . The process of causing histologic toxicity is thought to be related to the byproducts of degradation into cyanoacetate and formaldehyde . Further research showed that changing the type of alkyl chains in the compound to one with a longer molecular chain can reduce tissue toxicity . Cyanoacrylates are simple, inexpensive and practical adhesives. Cyanoacrylates have been used for achieving hemostasis at intraoral and extra-oral surgical sites treating ulcers, attaching grafts, managing cerebral spinal fluid leaks, stabilizing the bone fragments during plating, sealing sinus membrane perforations, and achieving peripheral nerve re-anastomosis; as periodontal dressings; and for a number of other dental applications  . They are sloughed from the surface of the skin and mucosa 7 to 10 days after adhesive application   . Butyl cyanoacrylate is a bacteriostatic, biodegradable, hemostatic cyanoacrylate with a long half-life and good tissue compatibility    . It can adhere in moist environments and is available in a formulation appropriate to be used in the oral cavity . It has been proven to be effective in closure of uninfected intraoral incisions on edentulous areas in the mandible, in extractions and periapical surgery     .
Few studies are focused on evaluating the wound healing and assessing patient-centered outcomes at the palate donor area after different harvesting techniques  . To the best of our knowledge, there is no study that compares different methods of wound closure at the donor site.
This prospective clinical trial aims at obtaining information to determine which technique from the patient's standpoint is superior.
The participants will be randomly assigned to one of two groups. The wound closure at the palatal donor area will be achieved with polytetrafluoroethylene (PTFE) sutures in one group and with high viscosity cyanoacrylate tissue adhesives on the other group. The surgical procedure will be performed by one of three calibrated periodontics residents (CS, JB, DR). Patients will be followed for 1 month post-operatively by the same resident to monitor the healing process and obtain patient feedback. Data will be collected at the baseline-day of the surgery, one day post-operatively and at the 1-week follow-up appointment. Randomization will be achieved using a computerized randomization scheme and will be communicated to the surgeon during the surgery by an independent examiner (AC). Participants will be block-randomized for each of the three operators for balance.
Anesthesia will be achieved with greater palatine block anesthesia and local infiltrations, if needed, on the palate with 1.8ml Lidocaine 2% 1:100,000 epinephrine. The single incision harvesting technique is chosen. Following administration for local anesthesia a single incision is made on the anterior hard palatal vault. The length of the incision depends on the size of the graft that is needed.
Once the graft is harvested pressure is applied to the palate until hemostasis is achieved and the graft is maintained in a moist environment.
Using 5-0 PTFE suture, continuous interlocking sutures 4mm apart are placed in the suture group leaving 3-4mm tails. Thin layers of cyanoacrylate are applied and rinsed with saline at least 3 times with interval at least 30s to allow complete polymerization in the cyanoacrylate group until hemostasis is achieved.
The harvested tissue graft is sutured to the donor site. The day of the surgery-a baseline record is obtained (see attached form). A loading dose of Amoxicillin 2g or Clindamycin 600mg, in case of allergy to penicillin, is provided to all participants immediately after the surgery with Ibuprofen 400mg for pain control. Postoperative instructions are also provided. They are also provided with an ice pack for the first 24 hours to minimize swelling from the recipient site. Sufficient amount of Ibuprofen 200mg is provided in a bag for the participants to consume 1-2 tablets po q4-6h PRN. They are instructed to return the bag for recording of the number of painkillers consumed at the 1-week follow-up appointment. A pain visual analogue scale (VAS) questionnaire with no pain on the left site and unbearable pain on the right site is given to the participants to note the level of pain from the palatal site the day after the surgery before the consumption of any painkillers. Participants are encouraged to contact the operator if they have any problem at any time.
Post-operative complications like severe bleeding, infection, abnormal pain, root exposure of the teeth adjacent to the donor site or sloughing, that need to be addressed before the scheduled appointments, will be recorded for 1 month after the surgery.
At the 1-week follow-up appointments the modified early-wound healing index (EHI)  , the wound length and width, and the presence of normal or abnormal inflammation will be recorded. The number of painkillers consumed the 1st week after the surgery will be counted and recorded. Participants will be asked to report any self-medication for pain. Sutures will be removed in the suture group. A 1-week follow-up VAS questionnaire is given to participants to fill during the 1-week follow-up appointment. The participants are asked to note the level of pain from the donor and recipient site and the level of discomfort (eating, speaking,.) from the donor site during the week after the surgery. Photos will be taken in all appointments.)
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
n-butyl cyanoacrylate and 2-octyl cyanoacrylate, 5-0 Polytetrafluoroethylene (PTFE) suture
Not yet recruiting
University of Manitoba
Published on BioPortfolio: 2016-10-18T02:08:21-0400
Inguinal incisions are the most frequent incisions used in children before the acquisition of continence (180 incisions per year for the Pediatric Surgery Department in Nice CHU). However,...
biologic glue is superior to traditional suturing for first degree perineal tears
The purpose of this study is to determine whether cyanoacrylate tissue adhesive is as effective as polyglactin 910 suture for surgical closure of cardiac device pockets.
The recent practice guideline recommends endoscopic injection of cyanoacrylate (GVO) is the preferred method to treat acute gastric variceal bleeding. The rebleeding rate remains high foll...
The purpose of this study was to test the hypothesis by comparing the efficacy of cyanoacrylate injection (GVO) and band ligation (GVL) in the treatment of acute GVH in liver cirrhotic pat...
The goal of this study was to assess the distal dispersion, the adhesion strength to catheter, the vascular toxicity and the ability in excluding embolized vessels using Purefill(®) (α-hexil-cyanoac...
The primary objective of this multicentre prospective observational study was to evaluate the early results of a new non-thermal embolisation method using N-butyl cyanoacrylate in venous insufficiency...
Cyanoacrylate(CA)-based tissue adhesives, although not widely used, are a feasible option to fix a mesh during abdominal hernia repair, due to its fast action and great bond strength. Their main disad...
Current guidelines recommend injection of cyanoacrylate as first-line therapy to prevent gastric variceal rebleeding. The method still poses a risk of ectopic embolism, which possibly correlate with v...
Cyanoacrylate (CYA) therapy has become an important component of the therapeutic toolbox of the interventional endoscopists with direct endoscopic injection accepted as first-line therapy of gastric v...
Cyanoacrylate tissue adhesive also used to occlude blood vessels supplying neoplastic or other diseased tissue.
Homopolymer of tetrafluoroethylene. Nonflammable, tough, inert plastic tubing or sheeting; used to line vessels, insulate, protect or lubricate apparatus; also as filter, coating for surgical implants or as prosthetic material. Synonyms: Fluoroflex; Fluoroplast; Ftoroplast; Halon; Polyfene; PTFE; Tetron.
Techniques for securing together the edges of a wound, with loops of thread or similar materials (SUTURES).
The application of a vacuum across the surface of a wound through a foam dressing cut to fit the wound. This removes wound exudates, reduces build-up of inflammatory mediators, and increases the flow of nutrients to the wound thus promoting healing.
Implants used in arthroscopic surgery and other orthopedic procedures to attach soft tissue to bone. One end of a suture is tied to soft tissue and the other end to the implant. The anchors are made of a variety of materials including titanium, stainless steel, or absorbable polymers.
Anything that breaks the skin is a wound because when the skin is broken, there's a risk of germs getting into the body and causing an infection. Follow and track Wound Care News on BioPortfolio: Wound Car...
In a clinical trial or interventional study, participants receive specific interventions according to the research plan or protocol created by the investigators. These interventions may be medical products, such as drugs or devices; procedures; or change...