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临床试验/NCT00000925
NCT00000925已完成2 期

Evaluation of High Protein Supplementation in HIV-1-Positive Subjects With Stable Weight Loss

National Institute of Allergy and Infectious Diseases (NIAID)19 个研究点 分布在 2 个国家目标入组 56 人开始时间: 1999年5月1日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
56
试验地点
19

研究概览

简要总结

The purpose of this study is to determine whether a high-quality protein food supplement will help HIV-positive patients maintain, and possibly gain, muscle mass.

Many HIV-positive patients lose weight that they are then unable to regain. This may be because patients are not eating enough protein or are not eating the right kinds of protein. The protein eaten in foods (such as meat, eggs, or beans) may not be able to make up for the amount of protein lost due to HIV infection. This study gives patients high-quality protein food supplements to help them maintain and/or gain weight.

详细描述

In many HIV-infected individuals with prior weight loss, the failure to regain weight and lean tissue is at least in part the consequence of inadequate protein intake or ingestion of a poor-quality protein rather than total caloric intake. Dietary sources of protein are presumably inadequate to meet the high metabolic needs caused by HIV infection. To achieve a target protein intake in the range (1.5 to 2.0 g/kg/day) demonstrated in other catabolic diseases necessary to achieve positive nitrogen balance and to generate substantial anabolic effects, this study will administer a supplement containing high-quality protein.

Two groups of 28 patients each are randomly chosen to receive either an oral nutritional supplement (Optimune) containing increased amounts of high-quality protein (whey), which is rich in cysteine and glutamine, or an isocaloric, identical-tasting supplement without added whey protein or amino acid supplementation. Weight, body composition, anthropometry, dietary intake, and general physical health are assessed at baseline and at Weeks 6 and 12. Plasma cysteine, glutathione, C-reactive protein, and prealbumin, along with urine IL-6, sTNFrII, and IL-1ra, are assessed at baseline and at Week 12.

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
Double

入排标准

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

入选标准

  • •You may be eligible for this study if you:
  • •Are HIV-positive.
  • •Are at least 18 years old.
  • •Have an HIV level less than 5,000 copies/ml within 30 days of study entry.
  • •Have lost weight in the past year, but your weight has remained fairly stable in the 2 months prior to enrollment.
  • •Are expected to live for at least 6 months.
  • •Are usually able to eat enough to maintain your present weight.
  • •Are able to complete a 3-day food diary.

排除标准

  • •You will not be eligible for this study if you:
  • •Have gained a significant amount of weight in the past 2 months.
  • •Have any opportunistic (HIV-associated) infections.
  • •Are unable to eat enough food for any reason, or are on tube feeding.
  • •Have nausea, diarrhea, or vomiting in the 14 days prior to study entry.
  • •Are being treated for diabetes.
  • •Are receiving chemotherapy or radiation therapy to treat cancer.
  • •Are pregnant or breast-feeding.
  • •Are allergic to milk or mangoes.
  • •Have an implanted defibrillator.

研究者

申办方类型
Nih
责任方
Sponsor

研究点 (19)

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