Birth

8

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

Condition / disease
Location
Status: Recruiting

Trial of Underwater Birth

Evaluate maternal perinatal outcomes in adult low-risk laboring people randomized to waterbirth compared to those randomized to birth on land.

Participants needed: 230
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: University of New MexicoUpdated: Apr 23, 2026Locations: 1
Eligibility criteria

≥18 years of age [+7]

Active infections such as HIV, Hepatitis B, Hepatitis C, HSV outbreak (on prophy... [+6]

Status: Not yet recruiting

Binaural Beat Music, Virtual Reality, and Hormones in Childbirth

This study aims to investigate the effects of Binaural Beats-supported music and virtual reality experience on the levels of oxytocin, prolactin, catecholamine, endorphin, prostaglandin E and cortisol, which are hormones that play an active role in birth, using the Elisa method. Additionally, the study will examine the effects of virtual reality experience and Binaural Beats-supported music during labor on labor pain and some birth outcomes (such as the presence of an episiotomy, the onset of labor, the duration of labor, and the newborn Apgar score).The randomized controlled study will consist of three groups: a virtual reality group, a Binaural Beats-supported music group, and a control group. The research will be completed with a total of 90 people, with 30 people in each group. The research will be conducted at the Maternity Ward of Istanbul Gaziosmanpaşa Training and Research Hospital. Ethics committee approval has been received for the research. Data collection has not yet begun. An application has been made to the hospital administration for institutional permission. The research will begin once the permissions are received.

Participants needed: 90
Trial details
Age: 20-35Biological sex: FemaleType: InterventionalSponsor: Medipol UniversityUpdated: Apr 8, 2026Locations: 1
Eligibility criteria

Able to speak Turkish and communicate verbally [+6]

Diagnosed with risky pregnancy [+5]

Status: Not yet recruiting

The Impact of Virtual Doula Services on Birth Outcomes in Rural Communities

This study will assess the impact of virtual doula care on birth and postnatal outcomes among rural mothers. The goal of virtual doula services is to improve access to care in underserved communities and decrease urban-rural differences in key maternal health outcomes including mode of birth (cesarean vs vaginal) and birth satisfaction. By implementing a digital randomized controlled trial, the study team will efficiently recruit a national sample of rural pregnant women to provide evidence of the effectiveness of virtual doula care, the appropriateness of virtual visits for different care and support needs, and the role of virtual care in improving maternal health.

Participants needed: 614
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: RANDUpdated: Dec 22, 2025Locations: 1
Eligibility criteria

18-45 years of age [+2]

non-singleton pregnancy [+3]

Status: Recruiting

Combined Intravenous Tramadol and Paracetamol Versus Intramuscular Pethidine for Pain Relief During the First Stage of Labor. Compare the Efficacy and Adverse Effects

The goal of this intervention study is to compare the efficacy and adverse effects of pain relief during the first stage of labor using 75 mg IM pethidine versus the combination of IV 100 mg tramadol and 1000 mg paracetamol. The investigator assume that the combination of IV tramadol and paracetamol will be more effective with less adverse effects than IM pethidine in pain relief at the first stage of labor. The investigator primary outcome is The effect on pain relief according to numeric rating scale (NTS) in the study groups Before the administration of the drugs, fetal heart rate patterns and contractions will be recorded with cardiotocography monitor for at least 20 min. The investigator will evaluate vigilance at 30 minutes following drug administration. NRS pain score (0-10) will be collected before administration and one hour after drug administration

Participants needed: 140
Trial details
Biological sex: FemaleType: InterventionalSponsor: Zohar NachumUpdated: Dec 15, 2025Locations: 1
Eligibility criteria

Previous cesarean delivery [+12]

Status: Not yet recruiting

The Effect of Wireless Electronic Fetal Monitoring on Labor Pain and Birth Experiences

This study is using Electronic Fetal Monitoring (EFM) to assess fetal health in pregnant women in labor. This will be compared with continuous wired EFM and continuous wireless EFM. The effects of wireless and continuous wireless EFM on labor pain levels and labor experiences will be measured.

Participants needed: 112
Trial details
Age: 19-35Biological sex: FemaleType: InterventionalSponsor: Tokat Gaziosmanpasa UniversityUpdated: Nov 18, 2025Locations: 1
Eligibility criteria

The study included healthy primiparous or multiparous pregnant women who agreed...

Pregnant women who were diagnosed with a risky pregnancy, who were illiterate, w...

Status: Recruiting

Childbirth Education Classes, Spousal Support, Birth Memory, Choice of the Birth Method, and Birth Satisfaction

The research questions of this study are listed below. 1. Is the mean spouse support score of pregnant women who attend childbirth preparation education with their spouses higher than that of women in the group with unique participation in childbirth preparation education and the control group who were left to usual care? 2. Is the mean birth satisfaction scale score of pregnant women who attend childbirth preparation education with their spouses higher than that of women in the group with unique participation in childbirth preparation education and the control group who were left to usual care? 3. Is the mean birth memory and recall scale score of pregnant women who attend childbirth preparation education with their spouses higher than that of women in the group with unique participation in childbirth preparation education and the control group who were left to usual care? 4. Are the birth preferences of pregnant women who attend childbirth preparation education with their spouses significantly different from those of women in the group with unique participation in childbirth prep

Participants needed: 93
Trial details
Age: 18-35Biological sex: FemaleType: InterventionalSponsor: Aydin Adnan Menderes UniversityUpdated: Jul 18, 2025Locations: 1
Eligibility criteria

Being able to speak and write Turkish [+3]

Having communication and psychological problems [+5]

Status: Recruiting

Birth & Breastfeeding Support Study

The goal of this observational study is to learn about the effects of birth practices such as cesarean section and vacuum assisted birth and diseases such as gestational diabetes and preeclampsia on exclusive breastfeeding. The main question it aims to answer is: • Does cesarean section, vacuum assisted birth, gestational diabetes and preeclampsia affect exclusive breastfeeding three months after birth? Participants answer eight online survey questions. One survey is distributed before birth and the remaining seven surveys are distributed after birth at three, seven and four-teen days, as well as one, three, six and twelve months after birth.

Participants needed: 1,628
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Herlev HospitalUpdated: May 28, 2025Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Effect of Snoezelen Room on Birth Process

Aromatherapy, visual and auditory stimuli are used together in the Snoezelen room. Aromatherapy increases the production of endorphins, reduces the intensity of pain and distracts the attention from the pain. Music also blocks the transmission of nerve impulses to the spinal cord.Considering these effects, the study emerges as a new technology for the midwifery field in our country. Although the use of snoezelen rooms in the delivery environment is becoming increasingly widespread abroad, it has not been used in delivery services in any hospital in our country. The primary purpose of this study is to convert a room in the delivery room of the hospital into a Snoezelen room and have women complete their delivery process in this room, and the secondary purpose is to determine the effect of the Snoezelen room on the delivery process. The primiparous pregnant women selected for the intervention and control groups will be informed about the purpose of the study and the applications by the research midwife or gynecologist following the birth and will be administered the "Pregnant Information Form", "Visual Analog Scale (VAS)", "Fear of Childbirth Scale", "Birth Comfort Scale", and after birth, the "Birth Information Form", "Birth Satisfaction Scale". The Beta Endorphin Level Recording Form will be filled out.

Participants needed: 104
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Sakarya UniversityUpdated: May 22, 2025Locations: 1
Eligibility criteria

Pregnant women who are planned to give birth vaginally in their 37th-42nd weeks... [+4]

Women with multiple pregnancies, [+7]