KCT0002553招募中未知
The effectiveness of Acupuncture for Post-surgical wound healing of proximal femoral fracture related to operation : pilot study
Catholic Kwandong University International St.Mary's Hospital0 个研究点目标入组 30 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 30
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 19(Year) 至 85(Year)（—）
- 性别
- All
入选标准
- •1. Patients who are between 19 and 85 years of age
- •2. Patients who underwent proximal femoral fracture surgery
- •3. Patients whose proximal femoral fracture surgery was performed using a specific suturing technique
- •· fasciorrhaphy were performed at 1cm intervals using Vicryl Plus Antibacterial Suture® #1, (ETHICON, Inc., Somerville, NJ).
- •· The subcuticular continuous suture technique was performed using Vicryl 4-0 to maintain dermal junction without leaving suture marks.
- •4. Those who agreed to participate and signed a consent form after being informed of the purpose and particularities of the clinical trial
排除标准
- •1. Patients with a medical history of the formation of hypertrophic scars and keloids in the skin
- •2. Patients with a medical history of vitamin C and zinc deficiency
- •3. Patients who use steroids or smoke during post-surgery hospitalization
- •4. Patients with allergic dermatitis
- •5. Patients whose participation in the study is difficult due to skin troubles or diseases developed pre-surgery
- •6. Patients with connective tissue disorder or hypoalbuminemia
- •7. Patients with diabetes (HbA1c>8%) or high blood pressure (at least 160mmHg in systolic blood pressure or at least 100mmHg in diastolic pressure) that cannot be controlled with diet therapy or medication
- •8. Patients with renal dysfunction (the serum creatinine level is at least twice the upper limit of normal) or chronic renal failure
- •9. Patients with hepatic dysfunction (the AST or ALRT is at least three times the upper limit of normal) or liver cirrhosis
- •10. Patients with thyroid dysfunction (In this case, those who are deemed capable of controlling the disease with a stable dose of medication over a 12-week period before the screening and capable of maintaining the same condition during the study can participate.)
- •11. Patients with hematologic, cardiac, lung, neurological, or mental diseases, or other serious systemic disorders that are unlikely to enable them to perform the clinical study
- •12. Pregnant, expecting pregnant or breast-feeding women
- •13. Patients who are participating in another clinical trial
- •14. Other patients whose participation is deemed inappropriate by the person in charge of the clinical study
研究者
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