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临床试验/NCT07705295
NCT07705295进行中(未招募)不适用

Prospective Controlled Clinical Trial to Evaluate the Safety and Effectiveness of Rib Osteotomy With Osteosynthesis Stabilization for Waist Narrowing

Research Inc1 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2026年2月20日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
160
试验地点
1
主要终点
Satisfaction of body results

研究概览

简要总结

The goal of this observational study is to learn about the long-term effects of RIBOSS intervention and demonstrate non-inferiority of postoperative respiratory function (FEV1, FVC, FEV1/FVC) at 6 months in the RIBOSS group compared with controls, using a non-inferiority margin of ≤0.10 L for FEV1 and FVC, and ≤0.05 for the ratio.

详细描述

Secondary Objectives:

  • To quantify hip circumference, change and waist-hip ratio improvement.
  • To compare intraoperative and postoperative pain levels (VAS) up to 1 month.
  • To assess radiological consolidation and plate angulation at 3 and 6 months.
  • To record early and late complications (Clavien-Dindo classification) up to 12 months.
  • To measure time to return to physical activity and overall satisfaction.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Candidates for elective waist narrowing through high-definition liposculpture.
  • Rib XI-XII projection ≥7 cm (CT-based).
  • Baseline spirometry within predicted limits.
  • Ability to provide informed consent and complete Body-QoL questionnaire.

排除标准

  • Prior thoracic surgery, trauma, or rib agenesis.
  • Osteoporosis or bone metabolic disease.
  • Chronic pulmonary or systemic disease.
  • Coagulopathy or psychiatric disorder limiting adherence.
  • Pregnancy or lactation.
  • Allergy to titanium implants.

结局指标

主要结局

Satisfaction of body results

时间窗: 1 day before surgery, 1 day after surgery, 7 days after surgery, 30 days after surgery, 3 months after surgery and 6 months after surgery

Body-QoL total score (0-100) from baseline to 6 months.

Change in waist circumference (cm)

时间窗: 1 day before surgery, 1 day after surgery, 7 days after surgery, 30 days after surgery, 3 months after surgery and 6 months after surgery

Change in waist circumference (cm), reduction of the waist circumference

次要结局

  • Safety Endpoint(1 week before surgery and 6 months after surgery)

研究者

发起方
Research Inc
申办方类型
Industry
责任方
Principal Investigator
主要研究者

Brian Ramirez, MD, MSc

MD, Aerospace medicine, MSc, PhD(c)

Research Inc

研究点 (1)

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