At Ideal Clinical Research (ICR), we specialize in women’s health clinical trials, ensuring successful recruitment, enrollment, and retention of participants. With access to board-certified OB/GYNs through our Principal Investigators (PIs), Sub-Investigators (Sub-Is), and network of referral sites, we provide the expertise and patient access needed for your next women’s health study.
Our investigators have conducted hundreds of women’s health clinical studies from Phase I through Phase IV. We streamline the study start-up process by utilizing a central IRB, ensuring faster approvals and execution.
Through a combination of our extensive patient database and targeted advertising strategies, we consistently meet or exceed enrollment goals while delivering high-quality data to our sponsors and CRO partners.
Our women’s health department is equipped to perform a range of specialized procedures, including:
• Transvaginal Ultrasound
• Colposcopy
• DEXA (Bone Densitometry) – through a trusted partner vendor
• Saline-Infused Sonohysterogram
• Endometrial Biopsy
Beyond execution, we collaborate with sponsors in the feasibility and planning stages, leveraging our therapeutic expertise to enhance study design and participant recruitment strategies.
Our sites have successfully completed clinical trials in a wide range of women’s health indications, including:
• Amenorrhea
• Adenomyosis
• Bacterial Vaginosis
• Contraception
• Dysmenorrhea
• Endometrial Hyperplasia
• Endometriosis
• Infertility
• Hormone Replacement Therapy (HRT)
• Hot Flashes
• Female Sexual Dysfunction
• Osteoporosis
• Overactive Bladder
• Urinary Incontinence
• Urinary Tract Infections
• Postpartum Depression
• Premenstrual Dysphoric Disease (PMDD)
• Premenstrual Syndrome (PMS)
• Human Papillomavirus (HPV)
• Uterine Fibroids
• Vaginal Atrophy
• Vaginal Dryness
• Vulvovaginitis
With a proven track record of excellence, ICR is your trusted partner for women’s health clinical trials. Contact us today to learn how we can support your next study
