跳至主要内容
临床试验/NL-OMON30865
NL-OMON30865尚未招募不适用

SIMULTANEOUS MEASUREMENT OF PELVIC FLOOR ACTIVITY, VAGINAL PLETHYSMOGRAPHY AND VAGINAL INNERVATION IN WOMEN WITH AND WITHOUT HYPERACTIVE PELVIC FLOOR SYNDROME. - HyPelM-study

Academisch Medisch Centrum0 个研究点目标入组 20 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
20

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • Inclusion criteria both groups:
  • 1. No sexual compaints for at least one year and sexually active.
  • 2. Heterosexual orientation.
  • 3. Willing to provide informed consent.
  • 4. Control group: Subjects are medically healthy and have no complaints that point to problems with the pelvic floor.
  • 5. Pelvic floor hypertonia group: Dyspareunia and co-morbidity of three or more symptoms that corrrelate with pelvic floor dysfunctions such as chronic abdominal pain, irritable bowel syndrome, constipation, diarrhea, urethra syndrome, overactive bladder, intercistal cystitis, vulvodynia, sexual arousal disorder, peri-anal pain, haemorrhoids, perineal pain, coccydynia, orgasm pain, lower back pain, muscle ache in other body parts such as neck or shoulders, headache, teeth gnashing, hyperventilation.

排除标准

  • Exclusion criteria both groups:
  • 1. Sexual complaints of shorter duration than one year.
  • 2. Pregnancy and lactation.
  • 3. Menstruation during measurement days.
  • 4. Use of medication negatively influencing sexual function or vaginal vasocongestion.
  • 5. Use of drugs 24 hours prior to testing.
  • 6. Affective, psychotic, or substance-abuse disorders.
  • 7. Pelvic floor hypertonia group: chronic pelvic floor hypertonia with generalized secundary vaginismus.

研究者

相似试验