Female

14

Review clinical trials related to Female. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Fluorocholine PET/MR in Breast Cancer

Objectives: Our study is conducted to use the pre-treatment FCH PET/MR in breast cancer patients, to investigate whether the conventional PET/MR imaging markers (SUVmax, MR spectroscopy-derived choline analysis, dynamic contrast-enhanced MRI, ADC analysis), and FCH/MR radiomic features, deep learning (DL) analysis are associated with molecular subtypes, clinical outcomes, treatment response, survival, and which parameters are more accurate for prediction purposes. Primary study purposes: -To investigate whether the pre-treatment FCH PET/MR imaging parameters are associated with molecular subtypes of breast cancers, and to evaluate the diagnostic performance for prediction purpose. Secondary study purposes: \- To investigate whether the pre-treatment FCH PET/MR imaging parameters are associated with the factors related to clinical outcomes (histologic grade, prognosis) and to analyze which parameters are more accurate for prediction purposes. Test drug: Name: 18F- Fluorocholine (18F-FCH) Dosage form: N-(\[18F\]fluoromethyl)-2-hydroxy-N,N-dimethylethan-1-aminium Strength: 3-5 MBq/kg per patient (5-6 mCi/mL at time of injection (TOI)) Dosage and administration: Intravenous injection. Selection criteria: 1. Women aged 25-75 years old. 2. Women diagnosed as breast cancer by pathological diagnosis from core biopsy within 3 months and who will receive neoadjuvant chemotherapy (NAC) before surgery; or women with pathologically proven breast cancer within 3 months and who will receive operation (without pre-operative neoadjuvant chemotherapy). 3. Women whose ECOG between 0-2 points and life expectancy ≧ 3 months.

Participants needed: 195
Trial details
Age: 25-75Biological sex: FemaleType: ObservationalSponsor: Taipei Veterans General Hospital, TaiwanUpdated: May 14, 2026Locations: 1Duration: 40 Weeks
Eligibility criteria

Women aged 25-75 years old. [+2]

Women who are unable to cooperate with the examinations [+8]

Status: Recruiting

Wild Blueberries for Gut, Brain, and Heart Health in Adults With High Blood Pressure

The purpose of the study is to determine the effectiveness of wild blueberries on cardiovascular health, cognitive function, and gut microbiota composition in non-Hispanic Black and White adults with elevated blood pressure.

Participants needed: 40
Trial details
Age: 45-65Biological sex: AllType: InterventionalSponsor: Georgia State UniversityUpdated: Mar 27, 2026Locations: 1
Eligibility criteria

Individuals 45-65 years of age [+3]

Allergies to berries [+7]

Status: Recruiting

Wild Blueberries for Gut, Brain, and Cardiometabolic Health in Prediabetes

The goal of this clinical trial is to determine the effectiveness of using a freeze-dried wild blueberry powder on cardiometabolic health, cognitive function, and gut microbiota composition in adult women with prediabetes.

Participants needed: 30
Trial details
Age: 20-65Biological sex: FemaleType: InterventionalSponsor: Georgia State UniversityUpdated: Mar 25, 2026Locations: 1
Eligibility criteria

Women aged 20-65 years old [+2]

Allergies to berries [+8]

Status: Recruiting

Physiological and Psychological Profiles

The participation of women in high-impact sports such as rugby and basketball has been steadily increasing in Saudi Arabia. These sports are known for their physical demands and competitive nature, which have heightened the incidence of sports-related injuries. Understanding the predictive factors for these injuries is critical for developing preventive strategies, reducing long-term health consequences, and reducing healthcare burdens. Therefore, this study aims to identify the predictive effect of physiological factors (e.g., muscle strength, anaerobic power, oxygen consumption) and psychological factors (e.g., self-efficacy, resilience) on sports injuries among female athletes in Saudi Arabia, particularly focusing on those involved in rugby and basketball. A prospective cross-sectional design will be employed, involving a total of 30 female athletes aged 18-35 years actively participating in rugby and basketball. Data will be collected at the lifestyle research center through a series of physiological assessments, including maximal oxygen consumption, anaerobic power testing, isokinetic muscle strength testing, and psychological evaluations using validated questionnaires. The findings are expected to provide insights into the specific factors that increase injury risk among Saudi female athletes, offering targeted strategies for injury prevention. These strategies aim not only to minimize injuries but also to reduce associated healthcare costs, thereby supporting the sustainable growth of women's sports in Saudi Arabia. Ultimately, this study seeks to contribute to the broader objectives of Vision 2030 by promoting a vibrant sports culture and enhancing public health.

Participants needed: 60
Trial details
Age: 18-45Biological sex: FemaleType: ObservationalSponsor: Princess Nourah Bint Abdulrahman UniversityUpdated: Mar 24, 2026Locations: 1
Eligibility criteria

Female athletes aged 18-35 years recruited from rugby and basketball teams in Sa... [+3]

Recent injury within the last six months that limits athletic performance Pregna... [+2]

Status: Recruiting

A Quantitative, Cross-Sectional and Observational Study to Characterize Age-Related Structural Changes in Facial Skin of Chinese Women Using Line-Field Confocal Optical Coherence Tomography (LC-OCT)

This is a single-center, non-interventional, observational, cross-sectional clinical study designed to quantitatively and qualitatively characterize skin properties in a cohort of 100 Chinese female Subjects aged 20 to 70 years. The study involves no product application and poses minimal risk to participants. The primary objectives are to establish a comprehensive skin aging profile database, characterize skin color, aging signs, and biomechanical properties, and create a histomorphometric database for the development and validation of ordinal photographic scales for aging research. Data will be collected through questionnaires, clinical assessments (including LC-OCT imaging), standardized photography, and non-invasive biophysical measurements. All procedures will be conducted in accordance with the ethical principles originating from the Declaration of Helsinki, the International Council for Harmonisation Good Clinical Practice (ICH-GCP) guidelines, and the relevant laws and regulations of China (including the \*Measures for the Ethical Review of Biomedical Research Involving Human Subjects\*). All data will be anonymized and stored securely.

Participants needed: 100
Trial details
Age: 20-70Biological sex: FemaleType: ObservationalSponsor: ChinaNormUpdated: Feb 17, 2026Locations: 1
Eligibility criteria

Chinese female, aged between 20 and 70 years (inclusive) at the time of signing... [+3]

Pregnant, planning pregnancy, or breastfeeding (as hormonal changes significantl... [+6]

Status: Recruiting

Dostarlimab, Cisplatin and Etoposide in Combination With Radiotherapy in Sandwich Sequence for Small Cell Neuroendocrine Cervical Carcinoma

Add-on dostarlimab to chemoradiation with etoposide and cisplatin and radiotherapy can improve progression-free survival (PFS) compared with historical controls who were treated with chemoradiation alone in SCNECC

Participants needed: 45
Trial details
Phase: Phase 2Age: 20-70Biological sex: FemaleType: InterventionalSponsor: Chang Gung Memorial HospitalUpdated: Jan 14, 2026Locations: 1
Eligibility criteria

Female participants who are 20-70 years of age on the day of signing informed co... [+4]

A WOCBP who has a positive urine pregnancy test within 72 hours prior to allocat... [+20]

Status: Not yet recruiting

Pain Neuroscience Education and Basic Body Awareness Therapy in Women With Chronic Pelvic Pain

This randomized controlled trial aims to investigate the effects of Pain Neuroscience Education and Basic Body Awareness Therapy, when added to standard physiotherapy and rehabilitation, on pain, autonomic nervous system responses, and pelvic floor muscle activity in women with chronic pelvic pain. A total of 45 women diagnosed with chronic pelvic pain will be randomly allocated into three groups: (1) standard physiotherapy and rehabilitation, (2) standard physiotherapy plus Pain Neuroscience Education, and (3) standard physiotherapy plus Basic Body Awareness Therapy. The study will assess pain intensity (algometry, NRS, SF-MPQ), pain catastrophizing, autonomic responses (electrodermal activity), pelvic floor muscle activation (EMG), and related psychological, cognitive, and body awareness parameters. Secondary outcomes will include sexual function, quality of life, and patient satisfaction. The aim is to compare two awareness-based interventions-one primarily mind-to-body (Pain Neuroscience Education) and the other body-to-mind (Basic Body Awareness Therapy)-to determine their relative and complementary effects on pain perception and physiological regulation in women with chronic pelvic pain.

Participants needed: 45
Trial details
Age: 20-65Biological sex: FemaleType: InterventionalSponsor: Sena ÖndeşUpdated: Jan 9, 2026
Eligibility criteria

Women with any type of chronic pelvic pain, including pelvic floor muscle dysfun...

Presence of pelvic infections, inflammatory conditions, or pelvic malignancy. [+5]

Status: Recruiting

Oral Mucosal Graft Versus Labial Graft in Female Urethroplasty

This study aims to compare the oral versus labial graft in female urethroplasty in female urethral stricture.

Participants needed: 40
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Tanta UniversityUpdated: Sep 4, 2025Locations: 1
Eligibility criteria

Female patients with urethral stricture. [+1]

Female patients with traumatic urethral stricture. [+1]

Status: Not yet recruiting

Exploring Pelvic Floor Dysfunction Among Egyptian Female Athletes

This Study is aiming to identify the prevalence of pelvic floor dysfunction in female athletes in Egypt and which sports contribute more in increasing their number. helping in gathering information about the risk factors and raising awarness about Pelvic floor dysfunction

Participants needed: 50
Trial details
Age: 16-60Biological sex: FemaleType: ObservationalSponsor: Cairo UniversityUpdated: Apr 13, 2025Duration: 1 Month
Eligibility criteria

Their age will range from 16 to 60 years. [+3]

Not currently involved in sports or physical activities. [+2]

Status: Recruiting

Fertility and Ovarian Reserve in Female Childhood Cancer Survivors

Ovarian function impairment affects the quality of life of the survivors of paediatric cancer by impacting fertility, bone quality and mental and cognitive health. The objective of this project is to evaluate the impact of low-intermediate dose alkylating agents associated or not with ovarian cryopreservation technique on ovarian function in female survivors of paediatric cancer. We propose to identify new epigenetic markers in order to predict the risk of premature ovarian insufficiency. The project will be led by a national multi-disciplinary team (paediatric oncologists, gynaecologists, endocrinologists). Paediatric cancer clinical data (therapy, fertility preservation, ...) will be extracted from the Paediatrics Late Effects database and additional data will be collected during PRINCESS fertility evaluation. Through translational and multi-disciplinary approaches, results should improve quality of life and fertility preservation in female survivors of paediatric cancer by developing new personalised screening tools for premature ovarian insufficiency.

Participants needed: 340
Trial details
Age: 18-50Biological sex: FemaleType: ObservationalSponsor: Centre Hospitalier Universitaire de LiegeUpdated: Nov 1, 2024Locations: 3Duration: 3 Months
Eligibility criteria

diagnosed with cancer1 between 01/01/2004 and 31/12/2018 [+4]

Cancer diagnosis for controls

Status: Recruiting

SEx-specific Differences in Cardiac Surgery Patients (SECS).

The aim of this study is to evaluate the differences between females and males undergoing cardiac surgery. The investigators will look at perioperative factors such as adaption of body weight, previous medical history, pharmacokinetics, transfusion, coagulation, cardiopulmonary bypass (CPB) related factors, cardiac function, inotropic requirements, risk, and outcome scores as well as morbidity and mortality at sort-term (within 30 days) and long-term (90 days and 1 year).

Participants needed: 10,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Jennifer BreelUpdated: Aug 15, 2024Locations: 1
Eligibility criteria

Patients > 18 years [+1]

None

Status: Recruiting

Epidemiology of Injuries in the Professional Women's Swedish National IceHockey League Permitted to Body-Checking

This research project can contribute to a deeper understanding of injury patterns among professional female ice-hockey players allowed to body check. An understanding of common injury types and mechanisms aids the clinician in diagnosis and management. This information can guide preventative strategies in the areas of education, coaching, rule enforcement, rule modifications, equipment improvement, and sportsmanship. Today, ice hockey is a sport associated with many severe injuries that not only causes suffering and lower quality of life for the athlete, but also costs society a lot of money. Reducing the number and severity of sport-related injuries is therefore of importance. Knowledge of the injury epidemiology of women's hockey could also contribute to better preventive training programs and other injury preventive actions in the sport. Currently, only a minority of all sports medicine research is made on female study participants (26). This research project has the possibility to gain more knowledge about the female athlete, not only applicable for elite hockey-players, but also for female athletes in different disciplines and in youth teams. Knowledge of factors associated with injury could also contribute to better injury preventive actions and highlight subgroups in extra need of future preventive interventions.

Participants needed: 225
Trial details
Age: 16-110Biological sex: FemaleType: ObservationalSponsor: Lund UniversityUpdated: Apr 8, 2024Locations: 1Duration: 5 Years
Eligibility criteria

minimum 16 years of age, registered player in the highest Swedish professional i...

age under 16 years.

Status: Recruiting

Towards a Sex-specific "Female Enhanced Recovery After Cardiac Surgery'' (F-ERAS) Pathway:

The aim of this study is to evaluate the differences between men and women undergoing cardiac surgery. We will look at perioperative factors such as body weight, body surface area, previous medical history, pharmacokinetics, transfusion, coagulation, cardiopulmonary bypass (CPB) related factors, cardiac function, inotropic requirements, risk, and outcome scores as well as morbidity and mortality at 30 and 90 days, 1, 5, and 10 years.

Participants needed: 5,500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Jennifer BreelUpdated: Dec 19, 2023Locations: 1
Eligibility criteria

Patients > 18 years [+2]

Status: Not yet recruiting

Efficacy of Transcutaneous Vagus Nerve Stimulation Paired With Tailor-Made Notched Music Therapy Versus Tailor-made Notched Music Training for Chronic Subjective Tinnitus

This clinical study is a prospective, multicenter, randomized, controlled, double-blind clinical study. Sun Yat Sen Memorial Hospital of Sun Yat sen University was the central unit, and Nanjing First Hospital, Sun Yat Sen people's Hospital, Guanfzhou Panyu central Hospital and Zhuhai integrated traditional Chinese and Western medicine hospital were the cooperative units. In this study, 388 patients with chronic subjective tinnitus were recruited. In view of chronic subjective tinnitus, a common ear disease, the study gave the patients three months of treatment with transcutaneous vagus nerve stimulation paired with tailor-made notched music therapy or tailor-made notched music training alone. By comparing the changes of subjective scale scores related to tinnitus before and after treatment in patients receiving two different therapies, such as THI, VAS, BAI, BDI, PSQI, to evaluate the efficacy of the two therapies, so as to judge whether transcutaneous vagus nerve stimulation paired with tailor-made notched music therapy is better than tailor-made notched music training alone. In addition, the study will continue to follow up the patients after the treatment for one year to observe the difference in the long-term sustained efficacy of the two therapies. This clinical study will also evaluate the two therapies from the perspective of compliance and safety, and explore the factors that affect the efficacy of the two therapies.

Participants needed: 388
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: Sun Yat-Sen Memorial Hospital of Sun Yat-Sen UniversityUpdated: Nov 27, 2023
Eligibility criteria

Patients with tinnitus as the main complaint: the patients subjectively feel the... [+4]

Patients with conductive deafness, history of middle ear surgery, pulsatile tinn... [+1]