跳至主要内容
临床试验/NCT01865838
NCT01865838终止不适用

A Study Into the Effect of Seprafilm on Post Operative Adhesions After Open Total Thyroidectomy.

National Cancer Centre, Singapore4 个研究点 分布在 1 个国家目标入组 19 人开始时间: 2013年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
19
试验地点
4
主要终点
Cricoid elevation

研究概览

简要总结

The investigators intend to determine the role of Seprafilm, a popular anti-adhesive agent in minimising internal adhesion formation in the neck after thyroid surgery and therefore reduce swallowing discomfort experienced by patients after surgery.

详细描述

Thyroid surgery not only constitutes one of the main pillars in the treatment of thyroid cancers, but is also employed in the management of symptomatic goitres. Occasionally, it is mandated in patients with thyrotoxicosis refractory to medical therapy. While thyroid surgery can be performed with low risks such that patients rarely have to stay beyond three days in hospital, the track record of thyroid surgery is somewhat blemished by the unfortunate side effects associated with the neck scarring after thyroid surgery. Not uncommonly, patients experience discomfort in the neck region after thyroid surgery; in the extreme of cases, patients may even complain of a lifelong pulling sensation in the neck area during eating.

The anti-adhesive properties of Seprafilm are well established in animal studies and affirmed by clinical observations in abdominal surgeries that utilize this material. Thus, Seprafilm is routinely used in instances when a surgeon foresees a need to perform abdominal surgery on the same patient in future, or during the fashioning of a temporary stoma. The safety profile of Seprafilm in thyroidectomy has also been shown by a recent study conducted by a group of clinicians in Seoul.

We postulate that the application of Seprafilm to the surgical wound towards the end of a thyroidectomy significantly reduces internal adhesion formation in the neck region. By achieving this objective, we hope to improve patients' satisfaction with thyroid surgery in terms of ease of swallowing after surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
21 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 21-75
  • Histological confirmation of differentiated thyroid cancer requiring surgery, symptomatic goiters, thyroid nodules requiring histological analysis, or thyrotoxicosis poorly controlled by medication.
  • Undergoing total thyroidectomy

排除标准

  • Previous neck surgery
  • Previous neck radiotherapy
  • Patients with a known history of keloids
  • Patients with a known history of motility disorders in the upper gastrointestinal tract and preexisting swallowing difficulty.
  • Patients with metastatic disease; patients with disease that would require postop radiation therapy, radionuclide iodine therapy and any adjuvant therapies.
  • Patients with advanced disease that would require radical or modified neck dissection
  • Patients with lobe larger than 10 cm, or nodule larger than 8 cm which require extensive dissection that may confound the study
  • Patients with connective tissue diseases and chronic diseases on long-term medications that may interfere with wound healings such as steroids

结局指标

主要结局

Cricoid elevation

时间窗: 1 to 14 days before the surgery, postop day 14 and 3 months postop

Trial candidates are to undergo videofluoroscopy to assess their swallowing and cricoid elevation is measured using ImageJ. * First measurement is 1 to 14 days before the surgery. * Second measurement is 14 days postop. * Third measurement is 3 months postop.

次要结局

  • Hyoid elevation(1 to 14 days before the surgery, postop day 14 and 3 months postop)
  • Crico-hyoid distance(1 to 14 days before the surgery, postop day 14 and 3 months postop)
  • Videotaping measurement(1 to 14 days before the surgery, postop day 14 and 3 months postop)
  • Swallowing Quality of Life questionaire(1 to 14 days before the surgery, postop day 14 and 3 months postop)

研究者

发起方
National Cancer Centre, Singapore
申办方类型
Other
责任方
Sponsor

研究点 (4)

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