跳至主要内容
临床试验/NCT05419609
NCT05419609Unknown不适用

Office-based Limited Dissection SMAS Manipulation Under Local Anesthesia Versus Facility-based SMAS Manipulation: a Single-surgeon, Random-assignment Non-inferiority Study

Dufresne, Craig, MD, PC2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2022年6月30日最近更新:
适应症

试验速览

阶段
不适用
入组人数
100
试验地点
2
主要终点
Difference in post-operative aesthetic correction rating between groups

研究概览

简要总结

To compare safety, patient satisfaction, and technical correction between a limited and full facelift, patients meeting strict clinical and safety criteria for both types of facelift will be randomly assigned to have one of these procedures. In the context of this study, a limited facelift is done in the office under local anesthesia, and a full facelift is done in the hospital or ambulatory surgical center with either general anesthesia or intravenous sedation.

详细描述

While there are previous reports of facelift in an office-based setting without general anesthesia or intravenous sedation, these reports included patient demographic information, medical history, and complication rates only and did not compare their office-based facelift with a full facelift done in the hospital or ambulatory surgical center. Previous reports also included oral sedation for all patients.

The current study will address these gaps in what is known about office-based limited facelifts done with local anesthesia. Finally, the study will also ascertain patient satisfaction at 3 points-at the pre-operative visit, early post-operative visit, and final visit-using selected modules from the validated FACE-Q | Aesthetics survey.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
40 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient willing to randomly undergo either a limited facelift done in the office or a full facelift done in the hospital
  • Patient willing and able to accept financial responsibilities of undergoing either type of facelift.
  • Patient able to provide informed consent
  • Between age 40-years-old and 85-years-old
  • No history of bleeding disorder
  • Stable weight
  • Does not have implanted cardiac device
  • Minimal anxiety
  • No history of smoking
  • Stable, good health
  • Normal blood pressure or well-controlled hypertension
  • Surgeon believes patient could tolerate and safely undergo either a limited facelift done in the office or a full facelift done in the hospital

排除标准

  • Patient refusal to randomly undergo either a limited facelift done in the office or a full facelift done in the hospital
  • Patient not willing or not able to accept financial responsibilities of undergoing either type of facelift.
  • Patient unable to provide informed consent
  • Under age 40-years-old or over 85-years-old
  • History of bleeding disorder
  • Unstable weight
  • Has implanted cardiac device
  • Significant anxiety
  • History of smoking
  • Significant active disease (e.g., dementia, cancer, chronic respiratory illness, heart disease, etc.)
  • Uncontrolled hypertension
  • Surgeon believes patient could not tolerate or safely undergo either a limited facelift done in the office or a full facelift done in the hospital

结局指标

主要结局

Difference in post-operative aesthetic correction rating between groups

时间窗: an average of 1 year following surgery

Post-operative aesthetic correction rating is completed based on comparison with pre-operative photographs. Ratings possible are 1 (no improvement) to 5 (excellent).

Difference between groups in number of patients requiring treatment by surgeon for post-operative adverse effects

时间窗: 1 hour following surgery and 2 weeks following surgery

Post-operative adverse effects may be acute, such as hematoma or infection, or they may become apparent later, such as nerve injury. Not all post-operative adverse effects will require treatment, such as mild pain, swelling, or bruising.

次要结局

  • Change in score of "FACE-Q | Aesthetics - Satisfaction With Lower Face and Jawline" from baseline to last post-operative visit(an average of 30 days before surgery and again an average of 1 year following surgery)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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