Clinical trials: Post-partum Recovery
Post-partum, Women
Creatine for Recovery and Thinking in Mothers
The purpose of this randomized, double-blind, parallel-group trial is to compare the effects of two doses of creatine monohydrate (5 g/day versus 10 g/day) administered for four weeks in postpartum women.
- Trial name
- CREATE-MOM (NCT07795853)
- Testing
- Creatine Monohdyrate
- Where
- United States
- Volunteers
- 40 people
- Sponsor
- University of North Carolina, Chapel Hill
Preeclampsia
Diuretics for Postpartum High Blood Pressure in Preeclampsia
The purpose of this study is to determine if furosemide administered after the first 24 hours of delivery, in women with severe peeclampsia and eclampsia accelerates high blood pressure control and diminishes hospital stay.
- Trial name
- DIUPRE (NCT02163655)
- Testing
- FUROSEMIDE
- Where
- Brazil
- Volunteers
- 120 people
- Sponsor
- Instituto Materno Infantil Prof. Fernando Figueira
Postpartum Pelvic Floor Function and Symptoms
Postpartum pElvic Assisted Recovery With Leva
The goal of this prospective cohort study is to evaluate the feasibility of postpartum pelvic floor muscle training using an FDA-cleared digital therapeutic motion-based device.
- Trial name
- PEARL (NCT06609317)
- Testing
- Digital therapeutic motion-based device
- Where
- 2 sites in United States
- Volunteers
- 25 people
- Sponsor
- University of South Florida
Urinary Incontinence, Pelvic Organ Prolapse (POP)
The RECOVER Study - Postpartum Recovery of Pelvic Floor Structures and the Impact of Early Rehabilitation
The goal of this observational study with an embedded pilot clinical trial is to learn how the pelvic floor recovers after vaginal childbirth and whether early individualized pelvic floor muscle training can improve recovery in…
- Conditions
- Urinary Incontinence, Pelvic Organ Prolapse (POP), Bowel Symptoms, Postpartum
- Trial name
- RECOVER (NCT07430865)
- Testing
- Early individualized pelvic floor muscle training (PFMT)
- Where
- 2 sites in Sweden
- Volunteers
- 380 people, healthy volunteers welcome
- Sponsor
- Vastra Gotaland Region
Postpartum Hemorrhage
rhuFVIIa in Post-partum Hemorrhage
The aim of this clinical research project is to evaluate the use of the recombinant human activated factor VII (rhFVIIa), given as a salvage therapy, in women with a dramatic postpartum hemorrhage still ongoing after all the…
- Trial name
- NCT00370877
- Testing
- rFVIIa, Standard Care
- Where
- 8 sites in France, Switzerland
- Volunteers
- 84 people
- Sponsor
- Centre Hospitalier Universitaire de Nīmes
Cesarean Delivery, Cesarean Section
Suzetrigine for Opioid-Free Recovery After Cesarean Delivery
The goal of this clinical trial is to determine whether suzetrigine increases the proportion of patients who remain completely opioid-free from completion of surgery through 72 hours after cesarean delivery.
- Conditions
- Cesarean Delivery, Cesarean Section, Pain, Postoperative, Opioid Consumption, Postoperative
- Trial name
- SPARE (NCT07534709)
- Testing
- Suzetrigine
- Where
- United States
- Volunteers
- 90 people
- Sponsor
- University of Texas at Austin
Recovery of Function
Postpartum Pelvic Floor Rehabilitation and Information Provided by the Health Care Providers
The aim of this work is to evaluate the experience of Postpartum Pelvic Floor Rehabilitation (PPFR) according to the information given by the health care providers.
- Trial name
- PPFR (NCT04882722)
- Testing
- Questionnaire
- Where
- France
- Volunteers
- 50 people
- Sponsor
- Centre Hospitalier Departemental Vendee
Pelvic Floor Disorders
Platelet Rich Plasma in Levator Ani Muscle Trauma
Levator trauma (ballooning) often occurs after vaginal delivery. Platelet rich plasma injection after delivery showed reduced hiatal area and maintain levator muscle strength.
- Trial name
- NCT03021954
- Testing
- Platelet Rich Plasma
- Where
- Indonesia
- Volunteers
- 116 people, healthy volunteers welcome
- Sponsor
- Dr Cipto Mangunkusumo General Hospital
Digital Intervention, Bibliotherapy
Digital Support Intervention for Pregnant People with Opioid Use Disorders
The goal of this pilot randomized feasibility study is to explore the benefits of providing parenting and recovery support for pregnant people with Opioid Use Disorders through digital technology (e.g. smartphones).
- Trial name
- PARENTSS (NCT06652880)
- Testing
- Digital technology, Bibliotherapy
- Where
- United States
- Volunteers
- 32 people
- Sponsor
- University of South Carolina
Postpartum Hemorrhage, Postpartum Period
Effects of an Interaction-Based Multi-Care Program on Postpartum Hemorrhage Recovery
This study explored the impact of an interaction standard theory-based multi-care program on postpartum recovery, coping styles, psychological distress, and quality of life in women experiencing postpartum hemorrhage (PPH).
- Conditions
- Postpartum Hemorrhage, Postpartum Period, Psychological Distress, Quality of Life
- Trial name
- NCT07058142
- Testing
- Interaction Standard Theory-Based Multi-Care Program, Conventional Nursing Intervention
- Where
- China
- Volunteers
- 110 people
- Sponsor
- Xingxing Lv
Postpartum Women
Postpartum Quality of Recovery & Maternal Satisfaction After C/S
Measuring patient-oriented outcomes and satisfaction is important to guide meaningful changes in obstetric anesthesia care. Quality of Recovery (QoR) scores are patient rated measures, which provide a global measure of recovery…
- Trial name
- QuReS (NCT05077891)
- Where
- Canada
- Volunteers
- 300 people
- Sponsor
- University of British Columbia
Opioid-Related Disorders, NAS
MOms in REcovery (MORE) Study: Defining Optimal Care
Northern New England has among the highest rates of opioid dependence in the U.S. This region also has among the highest rates of opioid-related deaths in the U.S., with a disproportionate high rate among pregnant women with…
- Conditions
- Opioid-Related Disorders, NAS, Substance Use Disorders, Mental Health
- Trial name
- MORE (NCT04251208)
- Testing
- Observational Study
- Where
- 10 sites in United States
- Volunteers
- 2,510 people
- Sponsor
- Trustees of Dartmouth College
Cesarean Section Complications, Postpartum Care
Using Empowered Relief and Education To Help Postpartum Women Recover After Cesarean Delivery
The purpose of this study is to study the effect of a pain relief skills session (Empowered Relief) and educational content on global postpartum recovery at 12 weeks post cesarean delivery.
- Trial name
- NCT07192718
- Testing
- Empowered Relief, Education
- Where
- United States
- Volunteers
- 80 people
- Sponsor
- Stanford University
Obesity, Maternal, Gestational Diabetes
Nutrition Optimization and Community Upliftment for Postpartum Recovery
The goal of this clinical trial is to better understand how different strategies, timing, and enhancements to medically tailored food delivery will address structural inequities in the food environment, empower communities to…
- Trial name
- NOURISH-GDM (NCT06445530)
- Testing
- MFeast ENHANCED, MFeast Usual Care
- Where
- United States
- Volunteers
- 40 people
- Sponsor
- Johns Hopkins University
Severe Preeclampsia
Role of Postpartum Furosemide in Recovery of Patients With Severe Preeclampsia
This randomized controlled trial will compare oral furosemide with placebo for improving blood pressure control in women with severe preeclampsia after delivery.
- Trial name
- NCT07861685
- Testing
- Furosemide and Potassium
- Where
- Pakistan
- Volunteers
- 434 people
- Sponsor
- Lady Reading Hospital, Pakistan
Quality of Life, Physical Activity
The Effectiveness of an Online Exercise Program on Well-being of Postpartum Women
The aim of this quasi-experimental study was to assess the effectiveness of a 6-week online exercise program on self-assessed quality of life (QoL), physical activity (PA), and dysfunctions of pelvic floor muscles of postpartum…
- Conditions
- Quality of Life, Physical Activity, Urinary Incontinence, Pelvic Organ Prolapse
- Trial name
- NCT06268782
- Testing
- Rehabilitate your core
- Where
- Finland
- Volunteers
- 308 people, healthy volunteers welcome
- Sponsor
- University of Turku
Diastasis Recti, Diastasis Recti Abdominis (DRA)
Effects of Visceral Manipulation Combined with Kinesio Taping on Diastasis Recti, Pain Intensity, Stress Incontinence, Pelvic Floor Strength, and Overall Wellness in Postpartum Women
This clinical trial aims to evaluate the effectiveness of different therapies for treating Diastasis Recti Abdominis (DRA) in postpartum women.
- Trial name
- NCT06723353
- Testing
- Visceral Manipulation Therapy, Abdominal Kinesio Taping, Combined Visceral Manipulation and Kinesio Taping
- Where
- Pakistan
- Volunteers
- 72 people
- Sponsor
- Health and Research-Insights
Laxity of Ligament, Pregnancy
Prenatal Pilates and Postpartum Ligamentous Laxity
Pregnancy induces hormonal and biomechanical adaptations that increase ligamentous laxity, which may persist into the postpartum period and contribute to joint instability, pain, and functional limitations.
- Conditions
- Laxity of Ligament, Pregnancy, Pilates Exercise
- Trial name
- NCT07344857
- Where
- Turkey (Türkiye)
- Volunteers
- 42 people
- Sponsor
- Ankara Medipol University
Cesarean Section
Longitudinal Study Evaluating Recovery After Scheduled Cesarean Delivery
The purpose of this research is to describe how patients recover after scheduled C-section for the first 3 months.
- Trial name
- NCT04462107
- Testing
- Surveys
- Where
- United States
- Volunteers
- 66 people, healthy volunteers welcome
- Sponsor
- Mayo Clinic
Hypertension, Pregnancy-Induced
Furosemide for Accelerated Recovery of Blood Pressure Postpartum
A randomized, double-blind, placebo-controlled single center investigation of furosemide's effect on postpartum blood pressure control in pregnancies affected by hypertensive disorders of pregnancy
- Trial name
- ForBP (NCT03556761)
- Testing
- Oral furosemide
- Where
- United States
- Volunteers
- 384 people
- Sponsor
- University of Pennsylvania