Delivery Complication

6

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

Condition / disease
Location
Status: Recruiting

Advanced Wireless Sensors for Neonatal Care in the Delivery Room

The goals of this observational study is to assess whether a new advanced wireless skin sensor vital sign monitoring system can effectively monitor the vital signs of healthy newborn infants (≥ 35 weeks gestational age). The main aims of this Study are to: 1. Assess feasibility 2. Evaluate safety 3. Determine accuracy of the wireless monitoring system, compared to the standard of care wired vital sign monitoring system, immediately after delivery and for the first 2h of age in the obstetrical center under unsupervised parents' care. The newborn infants participating in the Study will have both vital sign monitoring systems placed on their chest and limb. Their vital signs will be monitored for 2h consecutively.

Participants needed: 600
Trial details
Age: 35-42Biological sex: AllType: InterventionalSponsor: Guilherme Sant'Anna, MDUpdated: May 8, 2026Locations: 5
Eligibility criteria

Newborns ≥35 weeks (gestational age) [+2]

Newborns ≤ 35 weeks (gestational age) [+2]

Status: Recruiting

Training for Urinary Leakage Improvement After Pregnancy

This is a multi-center, randomized single-blind nonsurgical trial conducted in approximately 216 primiparous postpartum women at high risk for prolonged/sustained pelvic floor disorders with symptomatic, bothersome urinary incontinence (UI) amenable to nonsurgical treatment. TULIP is a 3-Arm trial with two active interventions (Arms 1 and 2) and a Patient Education control arm (Arm 3). Arm 1 consists of pelvic floor muscle training (PFMT). Arm 2 uses a home biofeedback device (leva®). The primary outcome will be assessed at 6 months postpartum by blinded outcomes assessors, and follow-up will continue until 12 months postpartum.

Participants needed: 216
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: NICHD Pelvic Floor Disorders NetworkUpdated: Dec 31, 2025Locations: 7
Eligibility criteria

≥18yo primiparous patient s/p singleton vaginal delivery (>32 weeks), approximat... [+5]

Inability to complete study assessments or procedures, per clinician judgment, o... [+6]

Status: Recruiting

Trends in the Administration of Tranexamic Acid for Postpartum Hemorrhage

Postpartum hemorrhage (PPH) is the global leading cause of maternal death, with 20-30% of maternal deaths in Thailand linked to hemorrhage. The WOMAN Trial (2017) provided strong evidence that administering tranexamic acid (TXA)within three hours of bleeding onset lowered PPH-related mortality by 31%. Consequently, the World Health Organization (WHO) updated its guidelines, recommending TXA as part of the standard treatment package for all PPH cases. Following this, the use of TXA has been widely adopted globally and increased in Thailand. A recent study at a major Thai university hospital observed a significant increase in TXA administration after 2017. The current study aims to further analyze the recent growth rate of TXA use and its impact on obstetric and perinatal outcomes during cesarean deliveries with PPH.

Participants needed: 648
Trial details
Biological sex: FemaleType: ObservationalSponsor: Mahidol UniversityUpdated: Dec 22, 2025Locations: 1
Eligibility criteria

1. Patients underwent cesarean delivery with primary postpartum hemorrhage

Gestational age at less than 24 weeks [+3]

Status: Recruiting

Effect of Oral Carbohydrate Intake > 44kCal Per Hour During Labour on the Rate of Instrumental Vaginal Delivery

Carbohydrate intake during physical exercise improves muscle performance and decreases fatigue. We hypothesized that carbohydrate intake during labor which is a period of significant physical activity can decrease the instrumental vaginal delivery rate. In a previous study we reported a trend toward a decrease in instrumental vaginal delivery and the mount of carbohydrate intake during labour. However due to some limitations no clear conclusion could be drawn. The present study is designed to examine the relationship between a high calory oral intake (\>44 kCal/hour during labour) and the rate of instrumental delivery.

Participants needed: 600
Trial details
Age: 18-60Biological sex: FemaleType: InterventionalSponsor: University Hospital, CaenUpdated: Jul 25, 2025Locations: 1
Eligibility criteria

nulliparous women [+4]

scheduled caesarean section [+6]

Status: Recruiting

Delivery Outcomes by AIDA (Artificial Intelligence Dystocia Algorithm) Analysis

Aims: Primary aim is to investigate outcomes of eutocic labor, evaluating intrapartum ultrasound parameters by AIDA method: Angle of progression (AoP), Asynclitism degree (AD), fetal head-symphysis distance (HSD), and midline angle (MLA). Secondary aim is to investigate outcomes of dystocic labor, evaluating intrapartum ultrasound parameters by AIDA method: Angle of progression (AoP), Asynclitism degree (AD), fetal head-symphysis distance (HSD), and midline angle (MLA). Tertiary aim is to investigate of neonatal outcomes of eutocic labor: Apgar scores at 1 min, Apgar scores at 5 min. Quaternary aim is to investigate of neonatal outcomes of dystocic labor: Apgar scores at 1 min, Apgar scores at 5 min.

Participants needed: 1,000
Trial details
Age: 20-45Biological sex: FemaleType: ObservationalSponsor: Centro di Ricerca Clinica SalentinoUpdated: Dec 3, 2024Locations: 2Duration: 12 Months
Eligibility criteria

pregnants in labor, at first pregnancy [+1]

Patients who are candidates for cesarean section. [+4]

Status: Recruiting

Time of Oxytocin Initiation at 2nd Stage of Labor and Adverse Outcomes

Early oxytocin administration at the 2nd stage of labor is associated with a higher rate of vaginal delivery, shorter second stage duration, and fewer adverse maternal and neonatal outcomes.

Participants needed: 120
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Rambam Health Care CampusUpdated: Dec 26, 2023Locations: 1
Eligibility criteria

Singleton pregnancy [+2]

Maternal age < 18 years' old [+3]