跳至主要内容
临床试验/ACTRN12622000726752
ACTRN12622000726752尚未招募未知

Efficacy of Capacitive and Resistive Electric Transfer (CRet) in the management of pain in Primary Chronic Pelvic Pain Syndrome in women: A randomized placebo-controlled trial.

niversidad de Castilla la Mancha0 个研究点目标入组 44 人开始时间: 2022年5月20日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
44

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
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
Female

入选标准

  • Women diagnosed of CPPS according to the definition by the European Urology Association (EUA).
  • - Presence of tenderness on palpation of Levator Ani (LA) muscle during vaginal examination.
  • - Presence of abnormal tension at rest within the PFM as indicated by surface electromyographic (EMG) signal (for the purpose of this study, this is defined as mean PFM EMG resting activity above 5 microV over a minimum period of 100 secs).
  • - Pharmacological treatment had remained stable for a minimum of 4 weeks prior to initiation of CRet therapy.
  • - Able and willing to provide informed consent.
  • - CRet treatment naive.

排除标准

  • - Pregnant or trying to get pregnant.
  • - Women presenting with an abnormal cell cytology on last smear test.
  • - Local malignancy/tumours.
  • - Women with a pace-maker fitted.
  • - Presence of open wounds in the treatment area.
  • - Presence of thrombosis/impaired circulation in the treatment area.
  • - Exposure to X Ray therapy or other ionizing radiations in the previous 6 months.
  • - Those with impaired/absent sensation in the treatment.
  • - Those unable to comprehend the physiotherapist’s instructions or who were unable to co-operate.

研究者

发起方
niversidad de Castilla la Mancha

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