You caught me just before going offline ;-) I'll take a quick stab at your question. I love educating if you haven't suspected already!
So...there really isn't a better way to manage the estrogenic effects of the zuclomiphene other than simply LIMITING the burden of zuclomiphene (via dosage adjustment of Clomid) based on the patient's sensitivity. This is superior to DIM, CDG, or AI. Now some patients tolerate the zuclomiphene fine even at higher Clomid dosages, some need much lower due to sensitivity...this is where working with an experienced practitioner is IMPERATIVE!
Also keep in mind that with the increase in testosterone with SUCCESSFUL Clomid treatment -> there will be a concurrent increase in E2. Now this is cumulative to the estrogenic zuclomiphene effect (thus an E2 level of 30pg/mL in a TRT guy isn't apples to apples comparable to an E2 level of 30pg/mL in a Clomid guy).. Hope that makes sense as that is a difficult concept for even most physicians that treat with Clomid (and not coincidentally a common reason for the failure of their Clomid treatment for their patients). Now that increase in endogenous E2 (again concurrent with the estrogenic zuclomiphene), IF CAUSING ISSUES - will respond to DIM, CDG, and if needed LOW dose anastrozole (with AI > DIM/CDG).
Hope this makes sense, even many physicians I try to educate on this cannot grasp it!
Dr Saya - fascinating info.
Any thoughts on how obesity in males determines the success/failure of clomiphene therapy, e.g. the higher the BF (i.e. morbidly obese) the more prone your guys are to feel like garbage with clomiphene due to high levels of existing aromatase in the body?
Is it possible that some other group had an interest in Androxal never becoming legal, like, say the manufacturers of testosterone cypionate?
Is it possible any of those companies could influence the FDA?
More likely, in my opinion, is that they had very poorly designed studies/data that didn't reflect a distinct advantage over the already existant clomiphene. I say poorly designed studies/data as, based on our knowledge of the isomers, I would expect well designed studies WOULD show a distinct benefit. Time will tell.
Dr Saya, first of all - many thanks for you sharing this essential knowledge with us.
We all know Clomid causes increase in LH, which then stimulates testes to produce more testosterone. Should we monitor how much it raises LH? Is there some maximum limit of LH beyond which overstimulation, desensitization of Leydig cells may occur?
My second question is - is there any method known to medicine that would increase the amount of Leydig cells in testes?
Trying Defy Restart; Hoping to Be a Unicorn https://www.excelmale.com/forum/showthread.php?6255-Trying-Defy-Restart-Hoping-to-Be-a-Unicorn
Why ? What is the reason for that? Mood, libido, something else ?
Tnx, Doc, I have misunderstood that Vince is trying to be the Unicorn
Dr. Justin, I have 400 ng/dl of testosterone at 22 y/o. If restart protocols fail, should I go on TRT?
Would Clomid be the best option for us to discuss during my consultation, or would another treatment be better.
I am in the process of getting a consultation with defymedical, I've had my labs done just waiting on the physical from my pcp.
I am a little anxious waiting since it seems like I've been dealing with these symptoms forever with no end in sight. I was trying to wait until my consultation but I'm not patient.
With that being said I am 29yo 175lbs, my total T levels have been 390, 410, and 452 being the most recent. I know these levels are not terrible, but i dont feel great. Free T ranging from 8 to 12. My LH is 4.3 which appears to be middle range. Would Clomid be the best option for us to discuss during my consultation, or would another treatment be better?
Thank you if you are able to answer. If not then i will talk with you during my consultation.