1. Introduction
This consent form is to inform you about the use of enclomiphene for the treatment of hypogonadism and to increase testosterone levels. Enclomiphene is not approved by the U.S. Food and Drug Administration (FDA) for this indication, and its use in this context is considered off-label.
2. Purpose of Treatment
The purpose of this treatment is to address symptoms associated with hypogonadism, such as low testosterone levels, and to potentially improve related clinical conditions.
3. Nature of the Procedure
Enclomiphene is administered orally. The dosage and treatment schedule will be determined based on your specific medical condition and response to treatment.
4. Potential Benefits
The expected benefits of enclomiphene treatment include an increase in testosterone levels and improvement in symptoms of hypogonadism.
5. Possible Risks and Side Effects
Like all medications, enclomiphene can cause side effects. These may include, but are not limited to, mood changes, vision disturbances, and other estrogen-related effects. The long-term risks are not fully understood due to the lack of FDA approval for this use.
6. Alternatives
Alternative treatments, including FDA-approved therapies for hypogonadism, lifestyle modifications, and other interventions, have been considered and discussed.
7. Voluntary Participation
Your decision to undergo this treatment is voluntary. You have the right to refuse or discontinue treatment at any time.
8. Questions and Information
You have the opportunity to ask questions about the treatment, and your questions have been answered to your satisfaction.
9. Consent
By signing this form, you acknowledge that you have read and understood the information provided, the risks and benefits of enclomiphene treatment, and consent to proceed with the treatment under the guidance of your physician.