G-Shot

 

The G-SHOT® (clinical description: G-Spot Amplification® or GSA®), is a simple, nonsurgical, physician-administered treatment that can temporarily augment the G-Spot in sexually active women with normal sexual function.

 

The G-spot is named for Dr. Ernest Grafenberg, who first described it in a 1950 article in the International Journal of Sexology. He found a highly erogenous zone inside the vagina that gets bigger when directly stimulated and that can lead to a powerful climax.

 

The G-Shot is for normal sexually functioning women. It is not for women who have sexual dysfunctions (problems with the female sexual response cycle: arousal, plateau, orgasm, resolution); relationship problems or emotional/psychological problems. Also patients who fit the normal criteria may experience varied to no effect at all.

 

 


 

The G-Shot® is a painless office procedure performed in your doctor’s office under local anesthesia. The actual injection usually takes less than 8 seconds and the total office visit time is usually less than 30 minutes. A specially designed speculum is used to assist in the delivery of a specified amount of natural filler product into the G-Spot after local anesthesia. The G-Shot® augments (enlarges) the G-Spot. This results in a G-Spot about the size of a quarter in width, and one fourth of an inch in height (meaning the projection into the vagina). Note that results do vary.

 

 


 

Before you try and schedule your first G-Shot® treatment consultation, you probably have some questions, such as: How long will it take? How long will the results last? When can I resume sex?

Here's what you might expect at the doctor's office from the moment you arrive until your procedure is done. (Please note that although this experience is typical, the routine at your doctor's office may be different.)

The day of your appointment. Allow time before your appointment for filling out forms and for consulting with the doctor or a member of his or her staff.

You may also be asked about your expectations for treatment and if you have any allergies or any condition that wouldn't make you a good candidate for the G-Shot.

Before the procedure. In the consultation process your doctor will educate you on the G-Spot and how to localize it. Your doctor will go over risks and complications verbally and he or she will give you written consent as well. It is important to the doctor that every patient is completely informed of the risks, complications and alternatives to the procedure (please see risk and complications). You will then go into the examination room alone and perform a self examination based upon the doctor’s instructions and after you are comfortable with the localization of the G-Spot you will notify the assistant and they will come in to start the procedure.

The procedure. You will be positioned on the examination table as if you are “getting a PAP smear” and the doctor will do a pelvic exam and measurement of the G-Spot based upon your direction. He will transfer this measurement to a ruler and then a special speculum. The speculum, which has the location of the G-Spot on it, will then be inserted into the vagina and then a small needle will be used to deliver a small amount of local anesthetic in the area of the G-Spot. Then the high molecular weight hyaluronan will be injected. After this a tampon is placed (the tampon is to be removed in 4 hours). The entire G-Shot® injection procedure takes approximately 10 minutes.

After the procedure. There's no recovery time needed. You're ready to get on with your day! The most common side effect following injection includes scant bleeding from the needle injection site.

Results. Within 4 hours you can resume normal sexual activity. Results can last up to 4 months. Results do vary.

 

G Spot Amplification™ or G-Shot is not an approved use of the high molecular weight hyaluronan by the FDA and is an off-label use. However, collagen injection into the vagina (trans-vaginal or trans-urethral) has been performed for many years for the treatment of a condition called intrinsic sphincter deficiency (ISD) which primarily affects elderly women. In ISD the internal urethral sphincter remains open and these women continuously leak urine. These techniques are also used for the treatment of stress urinary incontinence (involuntary loss of urine with laughing, coughing, sneezing, exercising etc). The G-Shot procedure is an off label use. Multiple “fillers” or bio-injectables are used as bulking agents to close the internal sphincter and provide continence. There are numerous clinical investigational studies reporting on the injection of collagen substances, fillers and bio-injectables into the vagina for conditions indicated above. The majority of the studies show that the techniques are safe and rarely have complications. Any sign of swelling, itching or redness or other occurrences at the procedure site should be reported to your surgeon.

Risks not necessarily related to allergic reactions include uncomplicated urinary tract infections, urinary retention, and urethral irritation. Uncommon complications such as periurethral pseudocyst formation and urethrovaginal fistula also have been reported. Other complications seen include bleeding, infection, abscess formation, open sores, scarring and lumpiness, which may persist over the amplification area. However, long term (> 1 year) data are lacking. Please see consent form for a comprehensive list of the risks and complications associated with the use of this product.


Nothing contained on this website is intended to represent a promise, guarantee or warranty that any patient who undergoes the G-Spot Amplification/G-Shot will achieve a particular result. Individual results do vary, and no responsibility is assumed for failure to achieve a desired result. The use of high molecular weight hyaluronan in this procedure is an ‘off label’ use, and utilization of this product, no promise or representation, guarantee or warranty regarding its use, benefit or other quality is made. No representations that the use of this product and this procedure is approved by the FDA or any other agency of the federal or state government is made.