DRKS00006176进行中(未招募)未知
Prospective, randomized clinical trial for the comparison of the voice protheses Phonax® and Provox II® - Phonax
Klinik und Poliklinik für Hals-, Nasen-, Ohrenheilkunde Leipzig0 个研究点目标入组 22 人开始时间: 2014年5月21日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 22
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized controlled study
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 80 Years(—)
- 性别
- All
入选标准
- •histologically verified, primary resectable Larynx/Hypopharynxcarcinoma
- •indikation for laryngectomy with primary creation of a tracheo esophageal fistula
- •planned curative resection (R0-resection)
- •stage II/IV A ollowing UICC (without T1)
- •low to slightly enhanced risk of anesthesia
- •adequate bone marrow-, liver- and kindneyfunction
- •Karnofsky-Index =70%
- •Age 18-80 Years
- •written informed consent
排除标准
- •tumorspezifc pre-treatment (chemotherapy, radiation therapy)
- •Metachrone or synchrone malignom (exception: basaliom or low-risk prostatecarcinoma) [In case of a controlled tumor at a different location with a treatment free intervall of more than 5 years, inclusion might be possible after consultation of the co-ordinating investigator]
- •life expectancy < 6 months
- •acute infection or fever
- •anamnestic HIV-infection or othe immune suppression
- •serious cardio-pulmonary concomittant disease (heart insufficiency grade III and IV following NYHA scale, myocardial infarction, angina pectoris, respiratoric insufficiency serious Asthma bronchiale, COPD (FEV1 <35%))
- •chronic disease with permanent therapy (uncontrolled Diabetes, rheumatoide Arthritis) particularly steroid therapy
- •other concomittant diseases, which exclude the patient from the trial from the perspective of the trial physician
- •analphabetism
- •intolerance regarding the materials of the voice protheses
- •experienced low patient's compliance
- •regular follow-up impossible (e. g. patient lives outside of Germany)
- •lack of or patial legal capcity of the patient
- •participation in another clinical trial or application of a not yet registered substancewithin 30 days before trial start
- •pregnant or nursing
- •fertile female patients (< 2 years after the last spontaneous menstruation) without effective contraception (implants, injections, oral contraceptives, intrauterine devices, vasectomized partner)
研究者
相似试验
已完成
不适用
Comparison of two techniques for collecting umbilical cord blood: on the mother (upper level) versus on the delivery table (bottom level)mbilical cord blood collectionPregnancy and ChildbirthUmbilical cord blood collectionISRCTN65689096Hospital Donostia (Osakidetza) (Spain)44
进行中(未招募)
1 期
Clinical trial about the therapeutic use of diatrizoic acid (Gastrografin®) in postoperative ileus.Postoperative paralytic IleusMedDRA version: 17.1Level: LLTClassification code 10033841Term: Paralytic ileusSystem Organ Class: 100000004856EUCTR2014-000473-39-ESFundacio Parc Taulí62
已完成
不适用
The Use of Intravenous Fluids in Acute Ureteric Colicreteric ColicUreteric ColicRenal and Urogenital - Other renal and urogenital disordersACTRN12610000227099Dr Adeline Wu70
已完成
3 期
A prospective, randomized, controlled trial to compare the effectiveness of endoscopic sphincterotomy with endoscopic papillary large balloon dilation for removal of bile duct stonesbile duct stones, ductal stonesJPRN-UMIN000013887Kansai Endoscopic Device Selection (EDS) Working Group60
已完成
不适用
Study to compare the clinical outcomes of coiled-end versus straight-end Swan-Neck peritoneal dialysis (PD) cathetersEnd stage renal disease requiring renal replacement therapyUrological and Genital DiseasesEnd-stage renal diseaseISRCTN05846916Shanghai Ruijin Hospital, Shanghai Jiaotong University, School of Medicine (China)80
