Clinical trials: Postnatal Complication
Hypertension, Pregnancy-Induced, Hypertension
Wearables to Define Postpartum Blood Pressure Trajectories and Facilitate Evidence-based Monitoring Guidelines
To better understand postpartum blood pressure changes, the investigators are proposing a study to monitor blood pressure after delivery in 100 patients who the investigators expect to have normal blood pressure (i.e.
- Conditions
- Hypertension, Pregnancy-Induced, Hypertension, Postpartum Preeclampsia, Postpartum Complication
- Trial name
- NCT06576544
- Testing
- BP Watch
- Where
- United States
- Volunteers
- 300 people
- Sponsor
- University of California, San Diego
Health Knowledge, Attitudes, Practice, Post Partum Depression
mHealth India Postnatal Health Intervention Effectiveness
The goal of this study is to assess the effectiveness of a culturally-tailored mobile interactive education and support group intervention to supplement standard postpartum care activities in comparison to standard care alone on…
- Conditions
- Health Knowledge, Attitudes, Practice, Post Partum Depression, Breastfeeding, Nutrition, Healthy
- Trial name
- Kushal Maa (NCT05268588)
- Testing
- MESSSSAGE intervention
- Where
- 3 sites in India
- Volunteers
- 2,100 people
- Sponsor
- University of California, San Francisco
Postnatal Depression
Impact of Giving Birth During the Covid 19 Pandemia on Postnatal Women's Depression
Postnatal depression is an important problematic in French population with approximatively 10 -20% of women who suffer from postnatal depression. This pathology may have strong negative impact on both women and neonate's health.
- Trial name
- DEPRECOVID (NCT04368208)
- Testing
- Assessment of postnatal depression using the the Edinburgh questionnaire between 4 and 6 weeks after delivery
- Where
- France
- Volunteers
- 501 people
- Sponsor
- Poitiers University Hospital
Postoperative Complications
After Cesarean Time Interval for Exercise (ACTIVE) Trial
The purpose of this study is to test whether or not activity restrictions after a cesarean section are warranted and if exercise can improve postpartum wellness.
- Trial name
- ACTIVE (NCT04345757)
- Testing
- Structured exercise
- Where
- United States
- Volunteers
- 200 people
- Sponsor
- Weill Medical College of Cornell University
Postpartum Complication
Effects of Manual Lymphatic Drainage and Therapeutic Ultrasound on Breast Engorgement
To find the combined effects of the manual lymphatic drainage with therapeutic ultrasound on breast engorgement, pain and self-efficacy in post - partum women.
- Trial name
- NCT06303232
- Testing
- MANUAL LYMPHATIC DRAINAGE, THERAPEUTIC ULTRASOUND
- Where
- Pakistan
- Volunteers
- 42 people
- Sponsor
- Riphah International University
Growth Failure, Preterm Birth
Impact of Colostrum Oropharyngeal Immunotherapy on Postnatal Growth in Preterm Infants
The goal of this clinical trial is to ascertain whether oropharyngeal administration of colostrum contributes to postnatal growth in very preterm infants (those born before 32 weeks of gestation).
- Conditions
- Growth Failure, Preterm Birth, Microbiota
- Trial name
- IOCOIOPGIPI (NCT07082881)
- Testing
- Colostrum, Normal Saline
- Volunteers
- 220 people
- Sponsor
- Suqian First Hospital
Urinary Incontinence, Urinary Tract Disorders
Comparison of Pelvic Floor Therapy and Yoga on Stres Urinary Incontinence Incontinence
The aim of this study is to compare the effectiveness of pelvic floor physical therapy (PFT) and therapeutic yoga training (TYT) for women who have postnatal stress urinary incontinence (SUI).
- Trial name
- NCT05253898
- Testing
- Pelvic floor Physical Therapy, Therapeutic Yoga Training
- Where
- Turkey (Türkiye)
- Volunteers
- 32 people
- Sponsor
- Hasan Kalyoncu University
Prenatal Anxiety, Prenatal Depression
Effectiveness of an Online Biopsychosocial Intervention to Improve Well-being and Mental Health During Pregnancy
This study aims to develop and implement a preventive intervention through a mobile application to help pregnant women feel better emotionally and cope with the changes of pregnancy in a more positive way.
- Conditions
- Prenatal Anxiety, Prenatal Depression, Wellbeing, Obstetrical Complications
- Trial name
- BienGestar (NCT06871397)
- Testing
- Biopsychosocial Cognitive Behavioral Intervention
- Where
- Spain
- Volunteers
- 228 people, healthy volunteers welcome
- Sponsor
- University Rovira i Virgili
Hypertensive Disorders of Pregnancy, Pre-eclampsia
Ophthalmic Artery Doppler in the Puerperium After Hypertensive Disorders of Pregnancy (OPHELIA-PP)
Hypertensive disorders of pregnancy frequently fail to resolve at delivery. A substantial proportion of women remain hypertensive at the six-week postnatal review, postpartum eclampsia occurs days to weeks after birth, and a…
- Conditions
- Hypertensive Disorders of Pregnancy, Pre-eclampsia, Postpartum Hypertension, Puerperal Disorders
- Trial name
- OPHELIA-PP (NCT07841795)
- Where
- Italy
- Volunteers
- 366 people, healthy volunteers welcome
- Sponsor
- University of Roma La Sapienza
Postpartum Complication, Strength
Combined Effects Of Stability Oriented Breathing Exercises and Kegel's Exercises in Postpartum Women
The postpartum period often presents challenges such as increased inter-recti distance (diastasis recti), lumbopelvic pain, and reduced core strength.
- Trial name
- NCT07521085
- Testing
- Stability Oriented Breathing Training, kegels exercises
- Where
- 2 sites in Pakistan
- Volunteers
- 60 people
- Sponsor
- Riphah International University
Postpartum Depression, Postnatal Depression
Phase 2 Clinical Trial of GH001 in Postpartum Depression
This study is a multicenter, open-label, single-arm Phase 2 clinical trial. Approximately 15 female participants with clinically diagnosed postpartum depression (PPD) will be included in this study.
- Trial name
- NCT05804708
- Testing
- GH001
- Where
- 4 sites in Netherlands, United Kingdom
- Volunteers
- 10 people
- Sponsor
- GH Research Ireland Limited
Postnatal Depression
Community Singing Interventions for Postnatal Depression: a Hybrid Type II Effectiveness-implementation Trial
Postnatal depression (PND) affects over 13% of new mothers but there is still not an ideal treatment for all cases. Pharmaceutical and psychotherapy have offered solutions but there are challenges in treatment uptake and…
- Trial name
- SHAPER-PND (NCT04834622)
- Testing
- Melodies for Mums, Control Community Sessions
- Where
- United Kingdom
- Volunteers
- 400 people
- Sponsor
- King's College London
Postnatal Depression, Postpartum Depression (PPD)
Qualitative Study on the Experiences of Mothers 6 to 12 Months After Their Participation in the Mother-baby Groups of the HUGS Study
The HUGS-QUALI study is a qualitative investigation that explores the experiences of mothers who participated in HUGS mother-baby therapy groups.
- Trial name
- HUGSquali (NCT07017621)
- Where
- 4 sites in France
- Volunteers
- 12 people
- Sponsor
- University Hospital, Toulouse
Premature Birth of Newborn
The Norwegian Family Centered Care Study
This study evaluates possible effects of two different NICU designs; by comparing traditional and Family Centered Care in terms of infant nutrition, health and growth, and coping by family.
- Trial name
- NCT02452580
- Testing
- Family Centered Care
- Where
- Norway
- Volunteers
- 77 people
- Sponsor
- Vestre Viken Hospital Trust
Postnatal Growth Disorder
Impact of Electrolyte Intake (Sodium, Phosphorus) on the Growth of Premature Newborns
Extrauterine growth restriction (EUGR) is a common complication in the medical management of premature newborns. The long-term consequences of EUGR are weight and height restriction, metabolic disorders, and neurodevelopmental…
- Trial name
- ELECTROGRO (NCT06506981)
- Where
- France
- Volunteers
- 684 people
- Sponsor
- Central Hospital, Nancy, France
Appendicitis Acute, Cesarean Wound Disruption With Postnatal Complication
Are Cesarean Section and Appendectomy in Pregnancy and Puerperium Interrelated?
It is not known whether appendectomy for acute appendicitis (AA) increases the Cesarean section (CS) rate and whether CS increases the likelihood of AA and appendectomy in the early puerperium.
- Trial name
- APPENDECTOMY (NCT04876547)
- Testing
- appendectomy
- Where
- Turkey (Türkiye)
- Volunteers
- 32 people, healthy volunteers welcome
- Sponsor
- Amasya University
Postpartum Complication, Maternal Hypertension
Safest Choice of Antihypertensive Regimen for Postpartum Hypertension
The purpose of this investigator-initiated randomized control trial is to determine whether oral Nifedipine versus oral Labetalol is superior in controlling high blood pressures in the postpartum period.
- Conditions
- Postpartum Complication, Maternal Hypertension, High Blood Pressure
- Trial name
- SCARPH (NCT05551104)
- Testing
- Oral Nifedipine, Oral Labetalol
- Where
- United States
- Volunteers
- 500 people
- Sponsor
- Loma Linda University
Postnatal Depression
Culturally Adapted CBT Based Guided Self-Help in Patients With Postnatal Depression
This is a randomized controlled assessor-blind clinical trial comparing CaCBT based guided self-help (using a manual titled Khushi Aur Khatoon) against treatment as usual (TAU)
- Trial name
- NCT04347499
- Testing
- CaCBT based guided self help using Khushi aur Khatoon Manual
- Where
- Pakistan
- Volunteers
- 140 people
- Sponsor
- Peshawar Medical College
Depression, Postpartum, Depression, Post-Partum
A Study to Assess the Safety and Efficacy of Oral LPCN 1154A in Women With Severe PPD
The purpose of this research study is to test the study drug, LPCN 1154A, as a possible treatment for postpartum depression (PPD).
- Conditions
- Depression, Postpartum, Depression, Post-Partum, Postpartum Depression (PPD), Post-Natal Depression
- Trial name
- NCT06979544
- Testing
- LPCN 1154A
- Where
- 18 sites in United States
- Volunteers
- 90 people
- Sponsor
- Lipocine Inc.
Premature Birth, Breastmilk Collection
Targeted Nutrition for Moderate to Late Preterm Infants
This study will be comparing the postnatal growth of moderate to late preterm infants in the Neonatal Intensive Care Unit (NICU) born between gestational ages of 30 weeks 0 days to 35 weeks and 6 days who are receiving enteral…
- Conditions
- Premature Birth, Breastmilk Collection, Postnatal Growth Restriction
- Trial name
- NCT05515614
- Testing
- Targeted Fortification, Enfamil Liquid Human Milk Fortifier
- Where
- United States
- Volunteers
- 34 people, healthy volunteers welcome
- Sponsor
- Loma Linda University