PHONE:  843-449-0803

 Thank you for visiting Magnolia OB/GYN Research Center today!


Are you Post-Menopausal and have Low Desire for Intimacy?  You may be eligible to join our clinical research study!
You may qualify for this study if:
  • Are 40-80 years of age
  • Postmenopausal
  • Be in a stable relationship with the opportunity for sexual activity at least once per month over the past 6 months or longer 
If you join the study, it may last up to 36 weeks.  You will receive study medications and medical tests at no cost to you.

Planning your life around Heavy Periods?  Consider a research study for uterine fibroids.

If you have been living with heavy periods due to uterine fibroids, participating in a research study may be an option.  The Asteriod Studies are research studies evaluating the safety and effectivenes of an investigational oral medication for uterine fibroids.

You may be eligible to participate if you:

  • Are 18 years or older
  • Have uterine fibroids or think you may have uterine fibroids
  • Experience frequent heavy periods and/or pelvic pain

If you qualify and decide to participate, you may receive:

  • Study medication and study-related care at no cost
  • Feminine hygiene products
  • Nonhormonal birth control, as needed
  • Close monitoring during regular visits with the study doctor and experienced staff
  • Reasonable compensation for time and travel

To learn more or see if you qualify visit:   www.womenandfibroids.com  or call 843-449-0803


*Females > 18 years of age.

*Confirmed cervical infection HPV16 and/or 18

*Abnormal PAP smear result of HSIL (High grade squamous intraepithelial lesion)

Participation requires 9 visits and 3 telephone calls over 22 months (88weeks) after signing the Informed Consent.  The study is to determine the effectiveness, safety and tolerability of the investigational product vs Placebo, over three doses, given IM (intramuscular) immediately following electroporation with CELLECTRA(TM) device.

For more info on HPV click here.


* Premenopausal women 18-49 years of age

*  Diagnosed with Endometriosis within the last 10 years which is documented by laparoscopy or laparotomy surgical procedure

*  Experiencing moderate to severe pain abdominal pain associated with Endometriosis off regular menstrual cycle

Participation requires 18 visits (typically every month) and 7 telephone visits over a period of 26-34 months after signing the Informed Consent.

Daily oral treatment vs. Placebo

Are you experiencing symptoms of Over Active Bladder? Frequency, Urgency and Urinary Incontinence or loss Loss of Bladder Control following the sudden urge to urinate that cannot be delayed?

You may qualify for this study if:
  • Adult female, > or equal to age 18 to 80 years of age
  • Experiencing these symptoms for > 6 months
If you join the study, it may last for up to 15 weeks.  You will receive study medications and medical tests at no cost to you.

If you would like more information, please contact us via one of the methods below and the Research Center will contact you shortly.

We are located on the second floor (Suite 203) of the Magnolia ObGyn Medical Building, 8203 Nigels Drive in Myrtle Beach, minutes from the Grand Strand Regional Medical Center off 82nd Parkway.

If you would like to find out how you can become a participant in one of the above clinical research studies, please call us at 843-449-0803 or email: ann@magnoliaobgyn.com

If you prefer, please fill out your contact information below and the Research Center will contact you shortly.

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I would like to be contacted by our Research Dept. about participation in a clinical trial. YesNo

Which trial are you interested in?

What is clinical research?

Clinical research is done to find out if a new medication is safe and effective. Researchers first develop a new drug in the laboratory. If it looks promising, it is evaluated in people in clinical trials. Carefully conducted clinical trials are the fastest and safest way to find new treatments that work. Patients who agree to participate in clinical research receive the new medication free of charge, are very carefully monitored and often are compensated for their time and travel expenses.

What can I expect if I choose to become involved in a clinical trial?

First you will be carefully screened to make sure that the study drug is appropriate for your health problem and that it would be safe for you. Then the study would be explained to you in detail and a consent form signed.

You are always free to stop participating at any time. A thorough medical history and physical would be done as well as blood work. You would be asked to come back to the office regularly so your response to the medication could be monitored. At the end of the study you would discuss with your doctor what further treatments you may need.

What are the benefits in participating in clinical research?

  • To be on a new and hopefully better treatment for your health condition that is not available to the general public
  • Regular monitoring of your health
  • Most studies provide compensation for your time and travel as well as the free medication and medical care while you are in the study
  • You are helping to bring new and better treatments for people who need them

Clinical Research Website, please click here and become educated about Clinical Trials.