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临床试验/NCT01513122
NCT01513122已完成4 期

Bone and Body Comp: A Sub Study of the SECOND-LINE Study

Kirby Institute7 个研究点 分布在 5 个国家目标入组 210 人开始时间: 2010年2月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
210
试验地点
7
主要终点
Mean Bone Mineral Density Changes From Baseline to 48 Weeks as Measured by DXA Scan

研究概览

简要总结

The use of anti HIV drugs (ART), and in particular a class of drugs known as nucleoside reverse transcriptase inhibitors (N(t)RTI), has been associated with changes in body fat and in particular loss of peripheral fat in the limbs. Low bone mineral density and osteoporosis are also common in HIV-infected patients. There appears to be some association between ART and bone loss, but this is poorly understood and requires further research. The SECOND-LINE study provides an opportunity to examine if a new anti-HIV drug (raltegravir) can result in greater increase in limb fat than a drug regimen containing N(t)RTI, which is currently standard of care. This study also provides an opportunity to examine if additional bone loss occurs with the second regimen of anti-HIV drugs and whether non-N(t)RTI regimens of ART used in second line therapy result in more or less bone loss than use of other classes of anti-HIV drugs such as protease inhibitors or N(t)RTI combinations.

It is hypothesized that subjects randomised into Raltegravir arm will demonstrate greater increases in limb fat and smaller reductions in bone density at the proximal femur over 48 weeks than those randomised into the control arm (LPV/r + 2-3N(t)RTIs).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • HIV-1 positive by licensed diagnostic test
  • Aged 16 years or older (or minimum age as determined by local regulations or as legal requirements dictate)
  • Have received first antiretroviral regimen consisting of an NNRTI plus 2N(t)RTIs for ≥ 24 weeks
  • No change in antiretroviral therapy within 12 weeks prior to screening
  • Failed first-line NNRTI + 2N(t)RTI combination therapy according to virological criteria defined by two consecutive (≥7 days apart) HIV RNA results of > 500 copies/mL
  • No prior or current exposure to HIV protease inhibitors and/or HIV integrase inhibitors
  • Able to provide written informed consent

排除标准

  • The following laboratory variables:
  • absolute neutrophil count (ANC) < 500 cells/µL
  • hemoglobin < 7.0 g/dL
  • platelet count < 50,000 cells/µL
  • ALT > 5 x ULN
  • Pregnant or nursing mothers
  • Participants with active viral hepatitis B infection defined by the presence in serum of hepatitis B surface antigen
  • Use of immunomodulators within 30 days prior to screening
  • Use of any prohibited medications (rifampicin, midazolam, triazolam, cisapride, pimozide, amiodarone, dihydroergotamine, ergotamine, ergonovine, methylergonovine, astemizole, terfenadine, vardenafil, and St. John's wort)
  • Intercurrent illness requiring hospitalisation
  • Active opportunistic disease not under adequate control in the opinion of the site Principal Investigator
  • Participants with current alcohol or illicit substance abuse that in the opinion of the site Principal Investigator might adversely affect participation in the study
  • Participants deemed by the site Principal Investigator unlikely to be able to remain in follow-up for the protocol-defined period

研究组 & 干预措施

Arm 1. Lopinavir / ritonavir + 2-3N(t)RTI

Active Comparator

LPV/r 200mg/50mg 4 tabs once daily or 2 tabs twice daily + 2-3N(t)RTI

干预措施: Lopinavir / ritonavir (Drug)

Arm 1. Lopinavir / ritonavir + 2-3N(t)RTI

Active Comparator

LPV/r 200mg/50mg 4 tabs once daily or 2 tabs twice daily + 2-3N(t)RTI

干预措施: 2-3N(t)RTI (Drug)

Arm 2. Lopinavir /ritonavir + raltegravir

Active Comparator

干预措施: Lopinavir / ritonavir (Drug)

Arm 2. Lopinavir /ritonavir + raltegravir

Active Comparator

干预措施: raltegravir (Drug)

结局指标

主要结局

Mean Bone Mineral Density Changes From Baseline to 48 Weeks as Measured by DXA Scan

时间窗: 48 weeks

Mean Limbs Fat Changes From Baseline to 48 Weeks as Measured by DXA Scan

时间窗: 48 weeks

次要结局

  • Mean Glucose Changes From Baseline to 48 Weeks(48 weeks)
  • Mean Total Body Fat Changes From Baseline to 48 Weeks as Measured by DXA Scan(48 weeks)
  • Mean Triglycerides Changes From Baseline to 48 Weeks(48 weeks)
  • Mean Total Cholesterol Changes From Baseline to 48 Weeks(48 weeks)

研究者

申办方类型
Other Gov
责任方
Sponsor

研究点 (7)

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