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临床试验/NCT01077921
NCT01077921已完成2 期

Phase II Study of Propranolol as Anti-Adhesive Therapy for Sickle Cell Disease

Laura M. De Castro, MD1 个研究点 分布在 1 个国家目标入组 31 人开始时间: 2010年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
31
试验地点
1
主要终点
SS RBC Adhesion (Epi -1d/cm2- vs. Sham) by Treatment

研究概览

简要总结

An open label, prospective, randomized cross-over phase II study in up to 60 sickle cell patients who are either homozygous for Hb S or have HbSB0 thalassemia. Initially, each patient will be treated for 6 weeks with placebo or a standard dose of propranolol (40 mg) every 12 hrs. This will be followed by a 2-week washout period after which, patients will receive the other treatment modality (placebo or propranolol).

We Hypothesize that propranolol administered in vivo on a daily basis for 6 weeks (1) will decrease baseline adhesion to endothelial cells and will substantially abrogate epinephrine-stimulated adhesion to endothelial cells, as measured in vitro; (2) will improve biomarkers of endothelial activation and dysfunction; and (3) can be safely used in patients with SCD. Thus, the use of propranolol in SCD may represent a safe and effective means of anti-adhesive therapy in SCD.

Study Objectives:

Primary Objective:

• To establish the safety and efficacy of long-term therapy with propranolol as an anti-adhesive therapy for SCD.

Secondary Objective:

• To evaluate changes in soluble markers of endothelial activation and dysfunction.

Correlative Science Objective:

• To determine whether response to propranolol therapy is associated with polymorphisms in genes encoding the proteins involved in the upregulation of Sickle Red Blood Cell (SS RBC) adhesion by epinephrine.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

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 by electrophoresis (HEP) of Hemoglobin (Hgb) SS or Hgb Sβ0 thalassemia (all patients followed at our clinic have HEP-confirmed diagnosis on file)
  • Age ≥ 18 years
  • Blood pressure (BP) Systolic ≥ 95mm Hg and Diastolic ≥ 50mm Hg
  • Heart rate (HR) ≥ 70 and ≤ 110 bpm
  • Oxygen saturation by pulse oximeter and at room air ≥ 92%
  • Hematocrit (Hct) ≥ 20% and Hb > 6.0 g/dL
  • Euthyroid status as indicated by normal Thyroid Stimulating Hormone (TSH)
  • SS RBCs obtained during screening period demonstrating an adhesion response to epinephrine of 40% over non-stimulated baseline adhesion to endothelial cells
  • Capacity to understand and sign informed consent

排除标准

  • History of vaso-occlusive episode during the 6 wks prior to screening
  • RBC transfusion during the 3 months prior to study entry
  • Ongoing pregnancy
  • History of heart failure, myocardial infarct (MI), bradyarrhythmias, conduction defects
  • History of asthma or reactive airway disease
  • History of thyroid disease
  • Renal insufficiency (BUN >21 mg/dL and/or Creatinine >1.4 mg/dL)
  • Use during the screening or study period of any of the following medications: antihypertensives, diuretics, thyroid replacement therapy, anti-arrhythmia medications, bronchodilators, inhaled steroids, insulin, or hypoglycemic medication
  • History of allergy to sulfonamides

研究组 & 干预措施

Propranolol

Experimental

Drug arm

干预措施: Propranolol (Drug)

Sugar pill

Placebo Comparator

Placebo arm

干预措施: Placebo (Drug)

结局指标

主要结局

SS RBC Adhesion (Epi -1d/cm2- vs. Sham) by Treatment

时间窗: Week 0 to 6 and week 8 to 14

The stickiness of SS RBC will be evaluated by a well-established in vitro assay of adhesion of SS RBCs to cultured endothelial cells using a flow chamber. Overall change of adhesion from baseline to post intervention( Week 0 to 6 and week 8 to 14) in unstimulated cells (Sham treated) vs. Stimulated Red Blood Cells (Epi-treated) at 1 dyne/cm2

SS RBC Adhesion (Epi -3d/cm2- vs. Sham) by Treatment

时间窗: Week 0 to 6 and week 8 to 14

The stickiness of SS RBC will be evaluated by a well-established in vitro assay of adhesion of SS RBCs to cultured endothelial cells using a flow chamber. Overall change of adhesion from baseline to post intervention( Week 0 to 6 and week 8 to 14) in unstimulated cells (Sham treated) vs. Stimulated Red Blood Cells (Epi-treated) at 3 dyne/cm2

SS RBC Adhesion (Epi -2d/cm2- vs. Sham) by Treatment

时间窗: Week 0 to 6 and week 8 to 14

The stickiness of SS RBC will be evaluated by a well-established in vitro assay of adhesion of SS RBCs to cultured endothelial cells using a flow chamber. Overall change of adhesion from baseline to post intervention( Week 0 to 6 and week 8 to 14) in unstimulated cells (Sham treated) vs. Stimulated Red Blood Cells (Epi-treated) at 2 dyne/cm2

次要结局

  • Overall Change of Plasma Levels of sVCAM-1(Week 0 to 6 and week 8 to 14)
  • Overall Change of Plasma Levels of sE-selectin(Week 0 to 6 and week 8 to 14)
  • Overall Change of Plasma Levels of sP-selectin(Week 0 to 6 and week 8 to 14)
  • Overall Change of Plasma Levels of sICAM-1(Week 0 to 6 and week 8 to 14)
  • Overall Change of Hemoglobin (Hgb) Levels(Week 0 to 6 and week 8 to 14)
  • Overall Change of Lactate Dehydrogenase (LDH) Levels(Week 0 to 6 and week 8 to 14)
  • Overall Change of Hematocrit (Hct) Levels(Week 0 to 6 and week 8 to 14)
  • Overall Change of Oxygen Saturation (02Sat) Levels(Week 0 to 6 and week 8 to 14)
  • Overall Change of Systolic Blood Pressure Levels(Week 0 to 6 and week 8 to 14)
  • Overall Change of Diastolic Blood Pressure Levels(Week 0 to 6 and week 8 to 14)

研究者

发起方
Laura M. De Castro, MD
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Laura M. De Castro, MD

Associate Professor

Duke University

研究点 (1)

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