Hey guys I am going to start my cycle here in a couple weeks. Its just a simple Test E cycle at 500 mgs/week for 12 weeks. i just wanna know what you think of this PCT plan i got for it. If you have any suggestions or tweaks i would like to hear them because there are so many ideas out there. I will be getting my bloodwork done before i start by the way. and i have nolva, clomid and Hcg on hand. This is my first cycle ive done in 5 years.
I was thinking of running it like this
Hcg- Begins after last pin at 2,500 IUs/week for two weeks
Nolva- was gonna run for 45 days at 20 mgs/day
Clomid-was gonna run for 30 days at 50 mgs/day
the nolva and clomid i was gonna run after the 2 weeks of Hcg. and by the way i have 20,000 ius of hcg total so if you guys think i should run it longer or more for any reason i def can!!
any advice on scheduling and dosing is much appreciated!
- do you know what the half life of HCG is?
No that's NOT a pimp question.
However it's relevant with respect to not only HCG, but darn near every other PED in use today, as a drugs half life provide a measure of its DOSING INTERVAL!
Let's look at your SERMS and see if the "half life" principle holds true. Hmm that odd bc the half life of both of these drugs approximates 72 hours?
So why then are these drugs dosed QD (every day) in both clinical trials and according to the manufactures recomendations?
Well the fact is the half life of 72 hours is that of the PARENT compound and NOT of the more metabolically active ingredient BYPRODUCT. And what's the half life of those byproducts, about 22 hours! Yep half lives are important VERY important mate.
The dosing?
The dosing your have suggested is what induces ovulation in for infertile females AND has been used in males for the same purpose, albeit on a more limited evidence basis for males
This dose has also been used for AIH in published CASE STUDIES.
But we really don't know if the dose required to reverse HTPA suppression caused by AIH necessitates a higher or perhaps even lower SERM therapy.
So what to do? Chose the dose that we know works (for infertility) and has a lower frequency of adverse effects.
The same also applies to the use of DUAL SERM PCT therapy IMO, as there's a paucity of published data on this form of treatment and is probably best reserved for established "PCT failure".
(I'll agree there may be exceptions but they don't apply here IMO)
Finally BLOOD WORK is critical in KNOWING whether many forms of therapy are effective, and PCT is certainly no exception.
When should you begin PCT?
That brings us back to HALF LIVES again! What is the half life of T-e?
Oh that's VERY IMPORTANT bc SERMS are useless when exogenous anabolic agents are floating around BLOCKING the release of LH, just like E-2 does, even though some of the suppressive effects of TT are due to aromatization.
I'll give us this one
5-7 days.
So if you follow some basic pharmacokinetics your peak will reach 5K at day one and DECREASE 50% every 5-7 days.
So 5k-0 / 2.5k @ 1wk/ 1.25k @ 2wks / 750 @ 3wks / 375 @ 4 wks
etc.
Well as you can see there's no sense in starting PCT any sooner than FOUR WEEKS (six weeks if preferred IME) after your last PIN if T-e is what your cycling.
Ok now learn how you can take advantage of an AAS half life and SHORTEN the PCT waiting interval by using T-p rather than T-e during the last few weeks of a cycle.
Use the same dose but change the half life to TWO DAYS, the half life of T-p