ISRCTN25938172已完成不适用
A randomised prospective study to compare the use of skin staples versus Dermabond tissue adhesive in the management of wound healing in patients undergoing thyroid and parathyroid surgery: a pilot study
Record Provided by the NHSTCT Register - 2005 Update - Department of Health (UK)0 个研究点目标入组 30 人开始时间: 2005年9月30日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 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
入选标准
- •Patients who are over the age of 18 years and undergoing thyroid or parathyroid surgery, have no known allergy to the products used in this study.
排除标准
- •Not provided at time of registration
研究者
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A prospective, randomised study comparing the use of Actifuse (trademark) Advanced Bone MatriX (ABX) synthetic bone substitute with INFUSE (registered trademark) in patients requiring posterolateral instrumented lumbar fusion.Degenerative disc disease that can be treated using Posterolateral Intertransverse Process Fusion and Internal Fixation achieved by pedicle screws and rods.Musculoskeletal - Other muscular and skeletal disordersSurgery - Surgical techniquesACTRN12609000548235ApaTech Ltd100
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A prospective, randomised study comparing the use of Actifuse™ ABX synthetic bone substitute with INFUSE® in patients requiring posterolateral instrumented lumbar fusion with interbody fusion also referred to as: APPRAISE T1 (A Prospective PLF Randomised Actifuse InfuSe Evaluation Trial 1) - APPRAISE T1Prospective trial participants will have been diagnosed with degenerative disc disease with a treatment option of decompression and Interbody Fusion with Posterolateral Intertransverse Process Fusion and Internal Fixation achieved by pedicle screws and rods.MedDRA version: 9.1Level: LLTClassification code 10024992Term: Lumbar disc diseaseEUCTR2009-012672-27-NLApaTech Limited
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1 期
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