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临床试验/NCT06543199
NCT06543199已完成不适用

Evaluation of the Effect of Hypericum Perforatum L and Hyaluronic Acid on Excisional

Ataturk University1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2024年1月2日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
45
试验地点
1
主要终点
assessment of pain at the donor site

研究概览

简要总结

The free gingival graft (FGG) procedure is one of the surgical approaches used to create a large area of adherent gingiva around the tooth and implant. As part of this procedure, one SDG at a time is harvested from the donor site of the secondary healing palate. The most common postoperative complications are pain, burning sensation and delayed wound healing at the donor site. Many agents have been used for years to reduce these complications, but so far none has been emphasized as the ideal agent. In this thesis, methods to improve the healing of the hard palate, the donor site for SDG surgery, and postoperative patient comfort will be compared.

详细描述

The free gingival graft (FGG) procedure is one of the surgical approaches used to create a large adherent gingival and keratinized zone around teeth and implants. As part of this procedure, SDG is harvested from the palatal donor area. The most common postoperative complications from the palatal donor area left to secondary healing are pain, burning sensation and delayed wound healing at the donor site. Various hemostatic agents, dressing materials, platelet-rich fibrin and analgesics have been used for years to reduce postoperative complications, promote wound healing and increase patient comfort. However, none of them has been emphasized as the ideal agent in the relevant literature. In this thesis, we will compare the methods that will improve the healing of the hard palate, which is the donor site for SDG surgery, and postoperative patient comfort. Hypericum perforatum L and hyaluronic acid will be compared by local application to the palatal rotator area.

It is aimed to investigate the postoperative effects of topical application of Hypericum perforatum L and hyaluronic acid (trade names; HYPERICUM PERFORATUM L Dr Özberk St. John's wort oil; hyaluronic acid: Gengigel Forte Gel) on the healing of surgical wounds created in the palatal donor area after SDG and its effects on wound healing. Hyaluronic acid is a non-sulfated polysaccharide component of the glycosaminoglycan family, which is also found in joint fluids, serum and various body fluids such as saliva and gingival groove fluid. Although it is present in all periodontal tissues, it is especially prominent in non-mineralized tissues such as gingiva and periodontal ligament. The highly biocompatible and nonimmunogenic nature of the action of hyaluronic acid, its bacteriostatic, fungistatic, anti-inflammatory, antiedematous, osteoinductive and pro-angiogenetic properties leading to the promotion of wound healing in various tissues have led hyaluronic acid to be of interest in the treatment of various diseases in medical fields such as orthopedics, ophthalmology and dermatology. In dentistry, hyaluronic acid has been used in tooth extraction sockets, temporomandibular joint treatment to accelerate the healing process and to make the healing period comfortable.

Plants have always played an important role in the improvement of human health in history. Hypericum perforatum, a member of the Hypericaceae family, has been recognized as a valuable herbal medicine. This plant contains hyperforin, flavonoids and hypericin. The olive oil extract of H. perforatum has long been used as both topical and oral medicine to treat cuts, burns, depression, hemorrhoids, diabetes and gastrointestinal ulcers. Studies have shown that H. perforatum increases collagen deposition, shortens the duration of inflammation and stops the migration of fibroblasts during wound healing.

Both agents have many areas of use that have been tried and found to be effective on wound healing. It is aimed to contribute to the literature by evaluating these two agents in terms of wound healing and postoperative patient comfort in the palatal donor area and at the same time evaluating them with a control group in which no agent was used.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •The patient is in need of free gingival graft (FGG) surgery,
  • •The patient's acceptance of the treatment,
  • •All oral plaque and bleeding scores less than 20%.
  • •Age between 18-60 years.

排除标准

  • •The patient does not need SDG surgery,
  • •The patient is a smoker,
  • •The patient has a systemic disease that will affect recovery,
  • •The patient is unable to attend follow-up sessions,
  • •Previous periodontal surgery,
  • •The patient is pregnant or lactating,
  • •The patient has used antibiotics, corticosteroids, anti-inflammatory, immunosuppressive drugs in the last 6 months.
  • •Tooth deficiency such that the patient cannot wear acrylic aligners
  • •Acute periodontal condition

研究组 & 干预措施

CONTROL

Experimental

Group in which no agent was used in the area left for secondary healing at the donor site.

干预措施: wound healing monitoring (Procedure)

HYPERICUM PERFORATUM L

Experimental

Group using hypericum perforatum L agent in the area left for secondary healing at the donor site.

干预措施: Local application of hypericum perforatum L to the wound site (Procedure)

HYPERICUM PERFORATUM L

Experimental

Group using hypericum perforatum L agent in the area left for secondary healing at the donor site.

干预措施: wound healing monitoring (Procedure)

HYALURONIC ASID

Experimental

Group using hyaluronıc acid agent in the area left for secondary healing at the donor site.

干预措施: local application of hyaluronic acid agent to the wound site (Procedure)

HYALURONIC ASID

Experimental

Group using hyaluronıc acid agent in the area left for secondary healing at the donor site.

干预措施: wound healing monitoring (Procedure)

结局指标

主要结局

assessment of pain at the donor site

时间窗: Days 1,2,3,4,4,5,6,7

Measuring and recording the pain score at the donor site with a vas

evaluation of chewing discomfort at the donor site

时间窗: Days 1,2,3,4,4,5,6,7

Measuring and recording the chewing discomfort score at the donor site with a vas

evaluation of burning in the donor area

时间窗: Days 1,2,3,4,4,5,6,7

Measuring and recording the burning score at the donor site with a vas

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Tugba Aydin

associate professor doctor

Ataturk University

研究点 (1)

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