Clinical trials: Parous Women
Vaginal Laxity
Correlation Between Vaginal Laxity and Delivery Mode
Evaluation of pelvic floor using 2D and 3D Transperineal Ultrasound
- Trial name
- NCT07517978
- Testing
- Transperineal Ultrasound
- Where
- Egypt
- Volunteers
- 150 people, healthy volunteers welcome
- Sponsor
- Assiut University
Urinary Incontinence, Anal Incontinence
Tridimensional Pelvic Floor Ultrasound and Quality of Life Scores Questionnaires in Nulliparous or Parous Women
Evaluation of the impact of the delivery in the system of suspension and sustentation of pelvic floor, by 3D ultrasound and quality of life questionnaires.nt
- Conditions
- Urinary Incontinence, Anal Incontinence, Sexual Dysfunction, Self Esteem
- Trial name
- NCT03656601
- Testing
- 3D pelvic ultrasound
- Where
- Brazil
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Federal University of São Paulo
High-Risk Acute Myeloid Leukemia, Relapse And/or Refractory AML
Effect of Donor Chose on the Outcomes of GVHD Prophylaxis Underwent the Combined Treatment of ATG/PTCy for Haplo-HSCT
This is a prospective, multicenter, cohort study. The high-risk, relapse and refractory AML patients were enrolled in this study.
- Trial name
- Donor chose (NCT06686173)
- Testing
- non-intervention study, donor selection
- Volunteers
- 114 people
- Sponsor
- Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
Diastasis Recti Abdominis (DRA)
Diaphragm and Breathing Muscle Characteristics in Women With and Without Diastasis Recti Abdominis After Childbirth
Diastasis Recti Abdominis (DRA) is a common condition experienced postpartum, in which the abdominal muscles separate along the midline of the abdomen due to stretching and thinning of the linea alba.
- Trial name
- DRA-BREATH (NCT07389993)
- Testing
- Ultrasonographic assessment of the diaphragm, Inspiratory muscle testing
- Where
- Greece
- Volunteers
- 42 people, healthy volunteers welcome
- Sponsor
- University of Patras
Pelvic Floor Disorders, Fecal Incontinence
Lateral Episiotomy or Not in Vacuum Assisted Delivery in Non-parous Women
Nulliparous women with a live singleton pregnancy in cephalic presentation past 34 gestational weeks will be randomized to lateral episiotomy or no episiotomy when operative vaginal delivery by vacuum extraction is indicated.
- Conditions
- Pelvic Floor Disorders, Fecal Incontinence, Dystocia, Fetal Hypoxia
- Trial name
- EVA (NCT02643108)
- Testing
- Lateral episiotomy
- Where
- 8 sites in Sweden
- Volunteers
- 717 people
- Sponsor
- Karolinska Institutet
Failed Induction of Labor
Foley Catheter Versus Dinoprostone Vaginal Insert for Induction of Labor in Parous Women at Term: A Randomized Trial
The purpose of this study is to assess the effectiveness and safety of transcervical foley catheter as compared to dinoprostone vaginal insertion for preinduction cervical ripening and labor induction in term parous women with…
- Trial name
- NCT01596296
- Testing
- Transcervical foley catheter, Dinoprostone 10mg
- Where
- South Korea
- Volunteers
- 154 people
- Sponsor
- Seoul National University Hospital
Stress Urinary Incontinence
Effectiveness of an 8-week Independent Cadence Retraining Program on Stress Urinary Incontinence in Parous Runners.
The purpose of this research is to assess the impact of an eight-week home cadence training program on stress urinary incontinence symptoms in parous women.
- Trial name
- NCT07829692
- Testing
- Cadence Increase, Cadence Maintenance
- Where
- United States
- Volunteers
- 66 people, healthy volunteers welcome
- Sponsor
- Mayo Clinic
Gestational Diabetes Mellitus
Long Term Effects of Gestational Diabetes Mellitus in a Population of Parous Women
The primary goal of this proposed research deals with estimating the risk of developing type 2 diabetes and metabolic syndrome in women with a history of GDM compared to women without a history of GDM.
- Trial name
- GDM (NCT01637727)
- Where
- Israel
- Volunteers
- 324 people
- Sponsor
- Shaare Zedek Medical Center
Labor Induction, Cervical Ripening
Safety and Efficacy Study of Misoprostol Vaginal Insert for Induction of Labour
The primary objective of the study was assessment of the efficacy of four dose reservoirs (25 mcg, 50 mcg, 100 mcg, 200 mcg) of intravaginal controlled release misoprostol administered for up to 24 hours.
- Trial name
- NCT00346840
- Testing
- Misoprostol vaginal insert 25 mcg, Misoprostol vaginal insert 50 mcg, Misoprostol vaginal insert 100 mcg
- Where
- 6 sites in United Kingdom
- Volunteers
- 124 people
- Sponsor
- Ferring Pharmaceuticals
IUD Insertion
Vaginal Dinoprostone Administration Prior to an Intrauterine Device Insertion in Multiparous Women.
To investigate whether vaginal dinoprostone administered before intrauterine device (IUD) insertion reduces failed insertions, insertion-related complications, and pain in multiparous women.
- Trial name
- NCT04046302
- Testing
- Dinoprostone
- Where
- Egypt
- Volunteers
- 160 people
- Sponsor
- Cairo University
Pain Relief
Comparison Between 2 Doses of Misoprostol Before Intrauterine Device
The purpose of the investigators' study was to evaluate whether misoprostol will improve pain scores .
- Trial name
- NCT02901561
- Testing
- misoprostol 200, misoprostol 400
- Where
- Egypt
- Volunteers
- 212 people
- Sponsor
- Assiut University
Contraception
LCS16 vs. COC User Satisfaction and Tolerability Study
To evaluate user satisfaction in young nulliparous and parous women (18-29 years of age [inclusive]), using LCS16 compared to a COC over a period of 12 months.
- Trial name
- NCT03074045
- Testing
- Levonorgestrel (Kyleena, BAY86-5028), Ethinyl estradiol and drospirenone (Yarina, BAY86-5131)
- Where
- 9 sites in Russia
- Volunteers
- 145 people
- Sponsor
- Bayer
Asymptomatic Condition
Investigating Diaphragm Thickness and Mobility in Healthy Parous and Nulliparous Volunteers Using RUSI
The purpose of this study is to evaluate the intra-rater and inter-rater reliability of diaphragm thickness and excursion measurements by applying Rehabilitative Ultrasound Imaging (RUSI) in a diverse cohort of healthy women…
- Trial name
- NCT06048237
- Testing
- Diagnostic Ultrasound Imaging of the diaphragm
- Where
- Greece
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- Evdokia Billis
Contraception
Dose-finding Study for the Ultralow-dose Levonorgestrel Intrauterine Contraceptive System (LCS)
The purpose of this study is to investigate if drug doses lower than the one released from Mirena® would be as effective for contraception as Mirena®.
- Trial name
- NCT00185380
- Testing
- Levonorgestrel IUS (BAY86-5028, G04209B), Levonorgestrel IUS (BAY86-5028, G04209C), Levonorgestrel IUS (Mirena, BAY86-5028)
- Where
- 35 sites in Finland, Hungary and 3 more
- Volunteers
- 742 people
- Sponsor
- Bayer
Uterine Anteflexion, Parous Women
The Variation in Uterine Flexion Angle Before and After Voiding in Parous Women.
Intrauterine devices (IUDs) account for approximately 25% of contraceptive methods used in France. However, their insertion can be painful for patients and challenging for practitioners, particularly due to the passage through…
- Trial name
- FLEXIMIX 2 (NCT07084766)
- Testing
- ultrasonography, pelvic
- Where
- France
- Volunteers
- 200 people
- Sponsor
- University Hospital, Brest
Graft-Versus-Host Disease(GVHD), Bone Marrow Transplantation
Low-Dose ATG/PTCy Plus Ivarmacitinib for aGVHD Prevention in Haplo-PBSCT From Parous Female Donors
Graft-versus-host disease (GVHD) is a major complication after allogeneic hematopoietic stem cell transplantation (allo-HSCT), significantly affecting survival and quality of life.
- Trial name
- PARITY (NCT07570745)
- Testing
- Low-dose ATG + PTCy + Ivarmacitinib
- Where
- China
- Volunteers
- 82 people
- Sponsor
- Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
Fear
Induction of Women With Fear of Labor
The purpose of this study is to evaluate the experience of labor in parous women induced because of fear of labor and, to compare the experience of parous women induced without fear of labor.
- Trial name
- NCT01424059
- Testing
- WEDQ-B (questionnaire)
- Where
- Sweden
- Volunteers
- 250 people
- Sponsor
- Uppsala University Hospital
Pelvic Floor Dysfunction; Vaginal Laxity; Bladder Neck Descent in Parous Women
Evaluation of Vaginal Laxity and Bladder Neck Descent in Parous Women Using 2D and 3D Transperineal Ultrasound
This study aims to evaluate vaginal laxity and bladder neck descent in women who have given birth, using non-invasive 2D and 3D transperineal ultrasound.
- Trial name
- VLBNDUS (NCT07491224)
- Volunteers
- 185 people, healthy volunteers welcome
- Sponsor
- Assiut University