JPRN-jRCTs041230054招募中3 期
Botulinum Toxin Type A for Preoperative Treatment of Abdominal Wall Hernia
Saito Takuya0 个研究点目标入组 30 人开始时间: 2023年6月30日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 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
入排标准
- 年龄范围
- >= 20age old 至 <= 80age old（—）
- 性别
- All
入选标准
- •1) For this study, patients with abdominal wall hernias with a hernia portal of 5 cm or more.
- •2) Patients with indications for abdominal wall hernia repair based on the preoperative evaluation.
- •3) Patients who are willing to comply with the research protocol.
- •4) Patients have signed a consent document approved by the Clinical Research Review Committee regarding participation in the study.
排除标准
- •1) Patients with active cancer. However, active cancer does not include intraepithelial carcinoma or lesions equivalent to intramucosal carcinoma that is considered curable by local treatment.
- •2) Patients with systemic muscle disease (myasthenia gravis, Lambert-Eaton syndrome, amyotrophic lateral sclerosis, etc.).
- •3) Women who may be pregnant or are lactating.
- •4) Patients who are allergic to Botox.
- •5) Patients with severe psychosis or psychiatric symptoms that make it difficult for them to participate in the study.
- •6) Patients who are deemed ineligible for surgery.
- •7) Patients with a serious medical condition that would make it inappropriate for the investigator to participate in the study.
- •8) Patients with a history of abdominal surgery that is inoperable.
研究者
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