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中文摘要
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我们针对 A 型肉毒毒素治疗疼痛性皮肤平滑肌瘤的初步研究将评估患者注射后疼痛是否得到缓解。鉴于疼痛通常具有主观性,我们以安慰剂对照和双盲的方式设计了这项研究。在研究期间,受试者将在研究访问时使用标准化疼痛评分量表并通过疼痛日记来评估他们的疼痛。受试者还将完成生活质量评估。由于这种情况很少见,而且患者很难前往 NIH 临床中心参与方案,因此累积进展缓慢。 2013 财年,我们招募了更多受试者参加临床方案。
英文摘要
Our pilot study of botulinum toxin-A for painful skin leiomyomas will evaluate whether patients receive pain relief after injection. Given the often subjective nature of pain, we have designed the study in a placebo-controlled and double-blinded fashion. For the duration of the study, subjects will rate their pain using standardized pain scoring scales at study visits and through a pain diary. Subjects will also complete quality of life assessments. Due to the rarity of this condition and difficulty for patients to travel to the NIH Clinical Center for protocol participation, accrual has been slow. In fiscal year 2013, we enrolled additional subjects to the clinical protocol.
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Effects of systemic and topical perturbations on human microbes
Botulinum Toxin for Painful Cutaneous Leiomyomas
Gene Expression Profiling and Clinical Characterization of Phototoxicity
Studies of Skin Microflora in Healthy Individuals and Atopic Dermatitis Patients
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