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Act-utilitarian assess clinical trial

A clinical trial of HIV-infected pregnant women in several African countries and Thailand used a placebo-control group to determine whether a lower, cheaper dose of AZT could substantially reduce the transmission of HIV from pregnant women to their fetuses. The results showed the less expensive AZT treatment (that could be more widely used in poorer countries) could indeed significantly reduce vertical transmission.
However, many questioned the morality of using a placebo (no-treatment) group, which deprived control subjects of an effective treatment that could have prevented many babies from being infected with HIV. How might an act-utilitarian assess his clinical trial.

 

 

 

Sample Solution

Assessing the Clinical Trial of HIV-Infected Pregnant Women from an Act-Utilitarian Perspective

Introduction

Utilitarianism is an ethical framework that focuses on maximizing overall happiness or well-being. Act-utilitarianism, a form of utilitarianism, assesses the morality of an action based on the consequences it produces for the greatest number of people. When applying act-utilitarianism to the clinical trial involving HIV-infected pregnant women, it becomes essential to evaluate the overall well-being and happiness that resulted from the trial, taking into consideration the potential benefits and harms.

Weighing the Benefits

  1. Reducing Vertical Transmission: The primary aim of the clinical trial was to determine if a lower-cost AZT treatment could effectively reduce the transmission of HIV from pregnant women to their fetuses. The results showed that the less expensive AZT treatment significantly reduced vertical transmission. From an act-utilitarian perspective, this outcome is highly beneficial as it directly prevents the transmission of HIV to babies, potentially saving numerous lives and improving the overall well-being of both mothers and infants.
  2. Wider Treatment Availability: The use of a cheaper AZT treatment has the advantage of being more accessible and affordable, particularly for poorer countries with limited healthcare resources. By demonstrating the effectiveness of this alternative treatment, the trial opens the possibility of reducing HIV transmission in regions where costlier treatments may be unaffordable. This broader availability can lead to improved health outcomes, reduced suffering, and increased well-being for a larger population.

Evaluating the Potential Harms

  1. Placebo-Control Group: One of the primary concerns raised about the trial was the use of a placebo-control group, which deprived control subjects of an effective treatment to prevent HIV transmission. From an act-utilitarian standpoint, the use of a placebo-control group can be seen as ethically problematic since it intentionally withholds a potentially life-saving intervention. This raises concerns about the well-being and suffering of the control group, as they were exposed to a higher risk of HIV transmission.
  2. Ethical Considerations: The use of a placebo-control group can be justified in some clinical trials, as it allows for rigorous evaluation of the treatment’s efficacy and safety. However, in this particular scenario, where the alternative treatment could potentially prevent HIV transmission, the act-utilitarian perspective would argue that the potential harm inflicted on the control group outweighs the benefits of the trial.

Balancing the Consequences

From an act-utilitarian perspective, the clinical trial’s overall moral assessment depends on weighing the benefits against the potential harms. In this case, while the trial successfully demonstrated the efficacy of a cheaper AZT treatment in reducing vertical transmission, the use of a placebo-control group raises significant ethical concerns. The potential harm inflicted on the control group, which could have been prevented with the alternative treatment, undermines the overall well-being and happiness of the participants.

Conclusion

Assessing the clinical trial of HIV-infected pregnant women from an act-utilitarian perspective highlights the importance of balancing the benefits and harms. While the trial’s results provided valuable information and potential benefits for a larger population, the ethical concerns raised by the use of a placebo-control group cannot be overlooked. In this case, an act-utilitarian would likely argue that the potential harm inflicted on the control group outweighs the benefits of the trial, emphasizing the need for ethical considerations and alternative study designs to ensure the well-being of all participants.

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