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临床试验/NCT05818462
NCT05818462已完成不适用

Effect of Pelvic Radiation Therapy on the Urinary and Musculoskeletal Systems of Survivors of Childhood Cancer

University of Colorado, Denver1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2023年7月11日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
32
试验地点
1
主要终点
Uroflow and Bladder Scan Results

研究概览

简要总结

The aim of this study is to measure and evaluate the effects of pelvic external beam radiation therapy (EBRT) on lower urinary tract (LUT) function and bone mineralization.

详细描述

The aim of this study is to measure and evaluate the effects of pelvic external beam radiation therapy (EBRT) on lower urinary tract (LUT) function and bone mineralization. The overarching hypothesis is that patients who received EBRT to the pelvis will have an increased rate of LUT dysfunction and osteoporosis even when controlled for chemotherapeutic exposures, using patients with similar chemotherapy regimens as controls. Between these two groups, the team expect to observe significant differences in both patient-reported outcomes and direct measures of LUT 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
2 Years 至 40 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Patients of any age who were treated were diagnosed in 2007 or later and received chemotherapy for solid tumor malignancy, with completion of therapy (whether chemotherapy or radiation) at least one year prior to study enrollment.

排除标准

  • Patients with known dysfunctional voiding prior to cancer treatment.
  • Patients with tumor resection of bladder, prostate or gynecologic organs will be excluded.

研究组 & 干预措施

Patients who received EBRT to the pelvis.

Childhood cancer survivors who were treated with chemotherapy and radiation therapy to the pelvis, with or without surgical intervention. This group will consist of both primary pelvic sarcomas as well as patients who received whole abdominal radiation that included bladder exposure.

干预措施: Uroflow testing (Diagnostic Test)

Patients who received EBRT to the pelvis.

Childhood cancer survivors who were treated with chemotherapy and radiation therapy to the pelvis, with or without surgical intervention. This group will consist of both primary pelvic sarcomas as well as patients who received whole abdominal radiation that included bladder exposure.

干预措施: Bladder Scan (Diagnostic Test)

Patients who received EBRT to the pelvis.

Childhood cancer survivors who were treated with chemotherapy and radiation therapy to the pelvis, with or without surgical intervention. This group will consist of both primary pelvic sarcomas as well as patients who received whole abdominal radiation that included bladder exposure.

干预措施: Dysfunctional Voiding Scoring System Survey (Other)

Patients who received EBRT to the pelvis.

Childhood cancer survivors who were treated with chemotherapy and radiation therapy to the pelvis, with or without surgical intervention. This group will consist of both primary pelvic sarcomas as well as patients who received whole abdominal radiation that included bladder exposure.

干预措施: DEXA Scan of pelvis and sacral spine (Diagnostic Test)

Patients who received EBRT to the pelvis.

Childhood cancer survivors who were treated with chemotherapy and radiation therapy to the pelvis, with or without surgical intervention. This group will consist of both primary pelvic sarcomas as well as patients who received whole abdominal radiation that included bladder exposure.

干预措施: Urine tests for specific biomarkers (Diagnostic Test)

Control cohort.

Childhood cancer survivors who have been treated for a sarcoma who did not receive pelvic radiation, and were treated with chemotherapy, with or without surgical intervention or radiation therapy (outside of the pelvis). These patients will be matched as closely as possible to Group 1 to match chemotherapy regimens, and sex.

干预措施: Uroflow testing (Diagnostic Test)

Control cohort.

Childhood cancer survivors who have been treated for a sarcoma who did not receive pelvic radiation, and were treated with chemotherapy, with or without surgical intervention or radiation therapy (outside of the pelvis). These patients will be matched as closely as possible to Group 1 to match chemotherapy regimens, and sex.

干预措施: Bladder Scan (Diagnostic Test)

Control cohort.

Childhood cancer survivors who have been treated for a sarcoma who did not receive pelvic radiation, and were treated with chemotherapy, with or without surgical intervention or radiation therapy (outside of the pelvis). These patients will be matched as closely as possible to Group 1 to match chemotherapy regimens, and sex.

干预措施: Dysfunctional Voiding Scoring System Survey (Other)

Control cohort.

Childhood cancer survivors who have been treated for a sarcoma who did not receive pelvic radiation, and were treated with chemotherapy, with or without surgical intervention or radiation therapy (outside of the pelvis). These patients will be matched as closely as possible to Group 1 to match chemotherapy regimens, and sex.

干预措施: DEXA Scan of pelvis and sacral spine (Diagnostic Test)

Control cohort.

Childhood cancer survivors who have been treated for a sarcoma who did not receive pelvic radiation, and were treated with chemotherapy, with or without surgical intervention or radiation therapy (outside of the pelvis). These patients will be matched as closely as possible to Group 1 to match chemotherapy regimens, and sex.

干预措施: Urine tests for specific biomarkers (Diagnostic Test)

结局指标

主要结局

Uroflow and Bladder Scan Results

时间窗: 1.5 years

aggregate measured by voiding time (seconds, s), total voided volume (mL), average uroflow rate (mL/s), maximum uroflow rate (mL/s), uroflow pattern or curve (bell-shaped, tower-shaped, staccato, interrupted or plateau), and post void residual (mL)

次要结局

  • DVSS Scores(1.5 years)
  • Number of Patients with Osteoporosis(1.5 years)
  • DEXA Scan Results(1.5 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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