Example Consent Form

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INFORMED CONSENT FOR TREATMENT WITH CJC 1295 and Ipamorelin

I seek the medical services of insert ______________ of ____________________ and their employees
(collectively ______________________ ). I am executing this consent to confirm my discussion with
insert Physician name and my understanding of the risks, benefits, and alternatives to treatment
with CJC 1295 and Ipamorelin. The goal and possible benefits of this therapy are to try and
prevent, reduce or control the dysfunction associated with the aging process, through hormonal
balancing, control of oxidative stress, and other clinically significant therapeutic agents. However,
I understand that this treatment may be viewed by the mainstream medical community as new,
controversial, and unnecessary by the Food and Drug Administration (“FDA”).

Benefits and General Information
CJC 1295 is an analog of the growth hormone releasing hormone (GHRH) which increases
endogenous growth hormone release. Ipamorelin is a selective ghrelin secretagogue which also
encourages endogenous growth hormone release. Together, these two peptides are synergistic to
increase serum growth hormone levels and thereby increase serum levels of IGF1 and IGFBP3.

2 . Risks
The following are examples of some of the possible specific risks/adverse reactions reported for
therapy that may be prescribed for me. Some of these risks/adverse reactions are for prescription
drugs derived from the official FDA labeling requirements for these drugs. At physiological blood
levels, there are not expected to be any significant risks/adverse reactions as long as full medical
disclosure is achieved from the patient during the total time of therapy.

By signing this form, I understand the possible risks associated with this treatment. For CJC 1295
and Ipamorelin adverse reactions include injection site redness, transient high blood sugar,
development of antibodies to CJC 1295, and water retention. These side effects are dose related
and usually eliminated by adjusting the dosage. This drug should not be used in patients with
known cancer.

I understand that _____________________ will monitor my treatment in an effort to prevent any side
effects, but cannot guarantee that I will not experience any side effects or adverse reactions. I
understand that, as with any health treatment, there is no guarantee I will obtain satisfactory
results through the use of this therapy. I understand the use of this treatment does not preclude
me from using other treatments as well, though I recognize that I should inform any practitioners I
am seeing about the various treatments I am using.

NOTE: DO NOT SIGN THIS FORM UNLESS YOU HAVE READ IT AND FEEL THAT YOU UNDERSTAND IT.
ASK ANY QUESTIONS YOU MIGHT HAVE BEFORE SIGNING THIS FORM. DO NOT SIGN THIS FORM IF
YOU HAVE TAKEN MEDICATIONS WHICH MAY IMPAIR YOUR MENTAL ABILITIES OR IF YOU FEEL
RUSHED OR UNDER PRESSURE.

I certify that I have read the foregoing Informed Consent, discussed the issues noted above, had
opportunities to ask questions, and agree and accept all of the terms above.

Patient Name: ________________________________________________________

Patient Signature X_____________________________________ Date:________

If someone other than the patient is signing this form, indicate the name of the person, title, and
authority to sign this form below.

Name: ____________________________________________________________________________

Title/Relationship to Patient: ______________________________

Please provide authority to sign document: _______________________________________

I have explained this Informed Consent and answered all questions, and informed the patient of
the available alternatives and of the potential risks. To the best of my knowledge, the patient has
been adequately informed and has consented.

Physician Name: _________________________________

Physician Signature: _______________________________ Date: ___________________

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