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临床试验/NCT03864939
NCT03864939尚未招募2 期

Randomized Pilot Study to Improve Postprostatectomy Incontinence and Potency by Application of Dried Human Amnion Graft

German Centre for Assessment and Evaluation of Innovative Techniques in Medicine1 个研究点 分布在 1 个国家目标入组 328 人开始时间: 2019年4月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
328
试验地点
1
主要终点
Change in urine loss

研究概览

简要总结

The investigators present a randomized trial of patients undergoing placement of dehydrated human amnion membrane (dHAM) around the neurovascular bundle (NVB) and vesicourethral anastomosis (VUA) during radical retropubic prostatectomy (RRP) in a tertiary center in Germany.

详细描述

Patients suffer under incontinence and impotence after RRP, improving techniques and studies are missing. The human amniotic membrane includes growth factors and unique immune tolerance which can improve tissue regeneration. The preliminary studies could prove the potential value of dHAM in the reconstruction of the urinary tract and nerve protection. The investigators initially present a randomized trial to improve postoperative continence and potency of patients undergoing placement of dehydrated human amnion membrane (dHAM) around the neurovascular bundle (NVB) and vesicourethral anastomosis (VUA) during RRP for the treatment of prostate cancer. RRP is performed in a standardized way by one experienced surgeon. The patients are randomized 1:1 to dHAM vs. placebo and blinded during the study period. The primary outcome is a postoperative continence measure as 24hrs pad test up to 12mos postoperatively. Secondary outcomes are potency, insufficiency of VUA, postoperative complications and biochemical recurrence. Using the T-test with an alpha of 0.05 and a power of 80% and expecting a drop-out of 20% of the patients, an adjusted sample size per arm of 164 patients is required.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

盲法说明

Patients are blinded during the study period.

入排标准

年龄范围
40 Years 至 80 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • patients with localized prostate cancer
  • indication for radical prostatectomy
  • no other treatment of prostate cancer
  • availability to informed consent

排除标准

  • preoperative incontinence (24hrs pad-test)
  • preoperative erectile dysfunction (IIEF-5 < 20)
  • metastasized or locally advanced prostate cancer in preoperative assessment
  • previous radiation of pelvis
  • previous prostate cancer therapy
  • psychiatric disease
  • participation at another study

研究组 & 干预措施

dHAM

Experimental

dHAM wrap is placed during RRP.

干预措施: dHAM (Drug)

Standard

Placebo Comparator

A standard RRP is performed.

干预措施: No dHAM (Drug)

结局指标

主要结局

Change in urine loss

时间窗: From baseline (1 week after surgery) to 12 months after surgery

Urine loss is assessed by 24 hrs pad-test (in gram)

次要结局

  • Biochemical recurrence(at 6 weeks, 3 months and 12 months)
  • Change in erectile function (EF)(From baseline (4 weeks before surgery) to 12 months after surgery)
  • Complications(perioperative, at 6 weeks, 3 months and 12 months)
  • Postoperative catheter removal(through study completion, an average of 1 year)

研究者

发起方
German Centre for Assessment and Evaluation of Innovative Techniques in Medicine
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dimitri Barski

Principal Investigator

Lukas-Krankenhaus GmbH

研究点 (1)

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