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临床试验/NCT02619552
NCT02619552已完成不适用

Impact of Medical Treatment on Sexual Function in Patients With Crohn's Disease

University of Maryland, Baltimore4 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2011年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
50
试验地点
4
主要终点
Assessment of Disease Activity

研究概览

简要总结

Crohn's disease is a chronic inflammatory condition of the intestines that causes abdominal pain, diarrhea, tunnels around the anus (fistulas), and extraintestinal symptoms. Effective medical treatments exist to treat the disease; however they can have significant side effects.

Previous studies have shown that sexual function is impaired in patients with Crohn's disease. It is likely that both the symptoms related to the disease, medications used to treat the disease, and surgery all impair sexual function in a variety of ways. For example, body image may be impaired, patients may be worried about bowel incontinence or unpleasant odors associated with diarrhea, patients may have significant pelvic pain secondary to perianal fistulas, or they may have painful intercourse from adjacent inflammation or scarring in the pelvis. The impact of medical treatment on patient's ability to regain sexual function is not known.

The investigators propose a 6 month study to compare sexual function before and after treatment in patients with Crohn's disease about to initiate therapy with an anti-TNF drug for treatment of perianal fistula or intestinal Crohn's or about to initiate therapy with steroids.

The investigators anticipate that the investigators will show that therapy with an anti TNF agent will result in a more rapid and greater return of sexual function than steroids. This information will be important to help counsel patients about the optimal treatment to begin for treatment of their Crohn's disease. Furthermore, it would be the first study to evaluate the impact of medical therapy on sexual function.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of Crohn's disease confirmed by standard criteria
  • Active luminal Crohn's disease defined by an HBI score of >4 or with draining perianal Crohn's disease a) Active perianal Crohn's disease defined a presence of draining perianal fistula on physical exam19
  • Patients with active luminal Crohn's disease must be initiating treatment with an anti-TNF agent (Remicade, Humira, Cimzia, or Simponi) or a steroid (prednisone, Entocort, or Uceris).
  • Patients with active perianal disease must be initiating therapy with an anti-TNF agent (Remicade, Humira, Cimzia, or Simponi).
  • Can understand written instructions in English

排除标准

  • Previous primary non-response to an anti-TNF
  • Uncontrolled medical or psychiatric disease (a. Degenerative neurologic condition, b.Unstable angina, c.Class III/IV congestive heart failure, d.Severe asthma or chronic obstructive pulmonary disease, e.Symptomatic peripheral vascular disease, f. Chronic renal insufficiency (creatinine > 2.0), g. Malignancy within the last 3 years (excluding squamous or basal cell cancers of the skin), h. Poorly controlled depression, mania, and schizophrenia, i. Active infection, j. Acquired immunodeficiency syndrome)
  • Inability to adhere to the protocol
  • Need for imminent surgery other than an exam under anesthesia
  • Under 18 years of age.
  • Pregnancy
  • Use of concurrent prednisone >30 mg per day in the anti-TNF groups

研究组 & 干预措施

Anti-TNF (Remicade, Humira or Cimzia) for luminal CD

All participants are required to undergo study visits at baseline, 2 months, and 6 months in addition to any other routine visits. Sexual function, body image, disease activity, quality of life, and depression scores will be measured at baseline and at each study visit during the 6-month study.

干预措施: Anti-TNF (Drug)

Anti-TNF (Remicade, Humira or Cimzia)for perianal CD

All participants are required to undergo study visits at baseline, 2 months, and 6 months in addition to any other routine visits. Sexual function, body image, disease activity, quality of life, and depression scores will be measured at baseline and at each study visit during the 6-month study.

干预措施: Anti-TNF (Drug)

Steroid (Prednisone or budesonide) for luminal CD

All participants are required to undergo study visits at baseline, 2 months, and 6 months in addition to any other routine visits. Sexual function, body image, disease activity, quality of life, and depression scores will be measured at baseline and at each study visit during the 6-month study.

干预措施: Steroids (Drug)

结局指标

主要结局

Assessment of Disease Activity

时间窗: 6 months

Harvey Bradshaw Index

Assessment of Quality of Life

时间窗: 6 months

Short Inflammatory Bowel Disease Questionnaire

Assessment of Body Image

时间窗: 6 months

Body Image Scale

Assessment of Perianal Disease Activity

时间窗: 6 months

Perianal Disease Activity Index

Assessment of Sexual Function

时间窗: 6 months

Sexual Function Questionnaire

Assessment of Depression

时间窗: 6 months

PHQ 9

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Raymond Cross

Professor of Medicine

University of Maryland, Baltimore

研究点 (4)

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