Clinical trials: Duration of Labor
Labor Pain
Efficacy of Peanut Ball Usage on Labor Pain, Support and Control, Anxiety, and Labor Duration
*Primary: To compare the control group, women in the experimental group will have lower level of labor pain after the intervention of peanut ball usage.
- Trial name
- NCT04204395
- Testing
- Peanut Ball
- Where
- Taiwan
- Volunteers
- 80 people, healthy volunteers welcome
- Sponsor
- Taipei Medical University
Labor Pain
Programmed Intermittent Epidural Bolus for Labor Analgesia During First Stage of Labor 2
Brief Summary: Until recently, at Mount Sinai Hospital, epidural analgesia for labor pain was delivered with a pump that could only provide continuous infusion of the freezing medication in combination of pushes of medication…
- Trial name
- NCT02758405
- Testing
- Bupivacaine, Fentanyl, Infusion pump
- Where
- Canada
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- Samuel Lunenfeld Research Institute, Mount Sinai Hospital
Health Knowledge, Attitudes, Practice
Act in Time -Implementation of Health Promotive Work-way in Primary Care Setting (AcTi)
The study will support implementation of a health promotive work-way in primary care setting by using external and internal facilitators, with the aim to identify effective implementation strategies and to evaluate intervention…
- Trial name
- AcTi (NCT04799860)
- Testing
- health promotive work-way
- Where
- Sweden
- Volunteers
- 12,000 people, healthy volunteers welcome
- Sponsor
- Region Örebro County
Labor
Bladder Drainage During Labor: A Randomized Controlled Study of Obstetric Foley Therapy
The goal of this study is to compare two clinically-relevant bladder drainage techniques. This is a randomized controlled trial with a single primary outcome of time to delivery.
- Trial name
- SOFT (NCT00959920)
- Testing
- Indwelling catheter, Intermittent straight catheterization
- Where
- United States
- Volunteers
- 139 people
- Sponsor
- Loyola University
Pulmonary Disease, Chronic Obstructive
Effect on Exercise Endurance and Lung Hyperinflation of Tiotropium + Olodaterol in COPD Patients.
The primary objective of this trial is to investigate the effect of 6 weeks treatment with tiotropium + olodaterol fixed dose combination inhalation solution on lung hyperinflation and exercise tolerance in patients with COPD.
- Trial name
- NCT01533935
- Testing
- Tiotropium + Olodaterol, Tiotropium, Olodaterol
- Where
- 33 sites in United States, Argentina and 6 more
- Volunteers
- 291 people
- Sponsor
- Boehringer Ingelheim
Alzheimer Disease and Related Dementias, Cognition
Home-Based Brain Stimulation for Motoric Cognitive Risk Syndrome
The objective of this study is to determine the effects of a 6-month, home-based personalized transcranial direct current stimulation (tDCS) intervention targeting the left dorsolateral prefrontal cortex on cognitive function…
- Conditions
- Alzheimer Disease and Related Dementias, Cognition, Mobility Disability
- Trial name
- TDCS4MCR (NCT06821568)
- Testing
- Personalized Transcranial Direct Current Stimulation (tDCS)
- Where
- 2 sites in United States, Israel
- Volunteers
- 128 people
- Sponsor
- Hebrew SeniorLife
ADHD
Metacognitive ADHD Telehealth Intervention for Work-performance Enhancement (Work-MATE)
Adults with Attention-deficit hyperactivity disorder (ADHD) experience poor occupational performance at work compare to adults without ADHD, manifested at tendencies toward unemployment, job instability, work accidents, and…
- Trial name
- NCT05270226
- Testing
- The Metacognitive ADHD Telehealth intervention for Work-performance Enhancement (Work-MATE)
- Where
- Israel
- Volunteers
- 46 people
- Sponsor
- Sara Rosenblum
Labor, Second Stage
Urinary Catheterization and Second Stage of Labor
Labor is divided into three stages: the first stage is from labor onset until full dilation, second stage is from full dilation until delivery of the baby, and the third stage from the delivery of the baby until the delivery of…
- Trial name
- cath2stage (NCT02198157)
- Testing
- urinary catheterization
- Where
- Israel
- Volunteers
- 184 people, healthy volunteers welcome
- Sponsor
- Raed Salim
Obese Adults
Adherence and Quality of Life Across Three Different Intermittent Fasting Protocols in Obese Working Women
In these recent years, Intermittent Fasting (IF) has become popular among the public and health fraternities not only because it produced evidence-based results as an alternative dietary approach in weight loss strategy, but also…
- Trial name
- IF (NCT07804329)
- Testing
- Adherence to the IF Protocol, Quality of Life
- Where
- Malaysia
- Volunteers
- 32 people
- Sponsor
- Suriana Md Akir
Decrease Labor Pain
Effect of Fentanyl on Pain Severity and Duration of Labor
Background: There are two methods of pharmacologic and non- pharmacologic for reducing pain of delivery. It is necessary to be known effect of these drugs on the mother and fetus during labor adverse.
- Trial name
- NCT01648595
- Testing
- Fentanyl
- Volunteers
- 70 people
- Sponsor
- Mashhad University of Medical Sciences
Cervical Ripening, Outpatient
Outpatient Cervical Preparation to Reduce Induction Duration in NTSV Women
This study is to compare 2 groups in nulliparous women undergoing cervical ripening for induction of labor. The study hypothesis is that outpatient cervical preparation with a foley catheter can reduce the induction of labor…
- Conditions
- Cervical Ripening, Outpatient, Patient Satisfaction, Nulliparous
- Trial name
- OCPRID (NCT03934918)
- Testing
- Treatment
- Where
- United States
- Volunteers
- healthy volunteers welcome
- Sponsor
- University of California, Davis
Preterm, Nutrition Disorder, Infant
The Effect Of Oral Motor Stimulation And Nonnutritive Sucking To The Time Of Transition To Oral Nutrition In Preterm
Oral feeding difficulty is one of the problems that preterm infants frequently experience due to poorly developed oral musculature.
- Conditions
- Preterm, Nutrition Disorder, Infant, Feeding; Difficult, Newborn
- Trial name
- NCT05310851
- Testing
- PIOMI and non-nutritive sucking
- Where
- Turkey (Türkiye)
- Volunteers
- 39 people
- Sponsor
- Eskisehir Osmangazi University
Shift Work, Eating Behaviors
The Feasibility of Overnight Time Restricted Eating and Impact on Glucose Levels in Shift Workers
The aim of this clinical trial is to assess whether it is feasible for shift workers to follow a time-restricted eating diet. The trial will investigate the impact of time-restricted eating on blood glucose levels during day and…
- Trial name
- TREsh (NCT06686667)
- Testing
- Time Restricted Eating
- Where
- Australia
- Volunteers
- 31 people, healthy volunteers welcome
- Sponsor
- Woolcock Institute of Medical Research
Labor Pain
Programmed Intermittent Epidural Bolus for Labor Analgesia During First Stage of Labor: A Sequential Allocation Trial to Determine the Optimum Interval Time Between Boluses of a Fixed Volume of 2.5ml of Bupivacaine 0.25% Plus Fentanyl 8 mcg/ml
Programmed intermittent epidural bolus (PIEB) is a technique of epidural analgesia in which boluses of local anesthetic solutions are injected into the epidural space at a fixed time interval.
- Trial name
- NCT03735771
- Testing
- Bupivacaine
- Where
- Canada
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- Samuel Lunenfeld Research Institute, Mount Sinai Hospital
Impotence
To Determine How Different Doses of Tadalafil Work on Getting and Keeping an Erection 26 or 36 Hours After Taking
Study to see how effective different doses of tadalafil are for getting and keeping an erection when sex is attempted after a certain number of hours.
- Trial name
- NCT00547508
- Testing
- tadalafil
- Where
- United States
- Volunteers
- 485 people
- Sponsor
- Eli Lilly and Company
Pulmonary Disease, Chronic Obstructive
Effect of Treatment BI 1744 CL (5 and 10 mcg) Versus Placebo on Exercise Endurance Time During Constant Work Rate Cycle Ergometry II
To compare the effects of BI 1744 CL versus placebo on exercise tolerance after 6 weeks of treatment in patients with Chronic Obstructive Pulmonary Disease.
- Trial name
- NCT01040793
- Testing
- Olodaterol (BI 1744), Olodaterol (BI1744)
- Where
- 19 sites in Austria, Belgium and 3 more
- Volunteers
- 157 people
- Sponsor
- Boehringer Ingelheim
Time Usage of ED Physicians
Physicians Work Distribution in a Danish Emergency Department
physicians in the Emergency Department spend their time on interviewing and examining patients, file documentation, communication with colleagues about the patients.
- Trial name
- NCT01722721
- Volunteers
- 9 people
- Sponsor
- University of Southern Denmark
Rheumatoid Arthritis
Time to DMARD (Disease-Modifying Anti-Rheumatic Drug) Treatment and Actual Work Limitation of Patients With Rheumatoid Arthritis in Turkey
The objective is to measure time delay from onset of symptoms to diagnosis and time to disease-modifying anti-rheumatic drug treatments in Turkish patients with rheumatoid arthritis.
- Trial name
- NCT01144598
- Where
- 21 sites in Turkey (Türkiye)
- Volunteers
- 356 people
- Sponsor
- Abbott
Labor Pain, Labor Duration
Effects of the Rebozo Technique During Active Labor on Labor Pain and Labor Duration in Primiparous Women
Study Description Childbirth is a physiological process often accompanied by severe pain and prolonged labor, which may negatively affect maternal well-being and increase the likelihood of obstetric interventions.
- Conditions
- Labor Pain, Labor Duration, Childbirth, Management of Delivery
- Trial name
- Rebozo Techniq (NCT07759479)
- Testing
- Rebozo technique, Routine Intrapartum care
- Where
- Turkey (Türkiye)
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Istanbul University
Labor Pain
Programmed Intermittent Epidural Bolus for Labor Analgesia During First Stage of Labor
Until recently, at Mount Sinai Hospital, epidural analgesia for labor pain was delivered with a pump that could only provide continuous infusion of the freezing medication in combination of pushes of medication activated by the…
- Trial name
- NCT02550262
- Testing
- Bupivacaine, Fentanyl, Infusion pump
- Where
- Canada
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- Samuel Lunenfeld Research Institute, Mount Sinai Hospital