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comparison of delivery outcomes between 2 methods of physiologic and traditional delivery

Title of proposal: comparison of delivery outcomes between 2 methods of physiologic and traditional delivery in women referred to norani shahid hospital in talesh in 2011-12

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201110153027N15
Enrollment
Unknown
Registered
2011-10-27
Start date
2011-10-23
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Delivery. Single spontaneous delivery

Interventions

Intervention 1: Physiological childbirth: according to the Country Guideline, it’s a method of natural childbirth, and Treatment approaches to alleviate include Non-medical Pain relievers: Aromath
she can use birth ball and there is no limitation during labor as well as she can freely choose any position
serum and oxytocin is not injected her in routine way
oxytocin injection is based on partograph. cardiac monitoring is not continuously
Episiotomy can be performed immediately if needed(according to method in proposal).it is notable that if it is necessary , I will be trained by an expert instructor who helps me getting my Birth certi
Physiological childbirth: according to the Country Guideline, it’s a method of natural childbirth, and Treatment approaches to alleviate include Non-medical Pain relievers: Aromatherapy is a way
Traditional childbirth: During the study, traditional childbirth is defined as : birth mother's hospitalization based on Obstetric Indications, continuous fetal heart rate monitoring(FHR), amniotomy i

Sponsors

Tabriz University of Medical Sciences, Department Scholarships
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria 1- Women aged between 18-35 years 2- Gestational age 37-42 weeks based on the first day of the last menstrual period or based on ultrasound in Gestational age prior to12 weeks. 3- singleton pregnancy with cephalic presentation 4- Having low-risk pregnancy (absence of chronic illness like heart disease, hypertension, lung disease, diabetes, anemia, urinary tract infection (UTI), thyroid disease, Epilepsy, no spontaneous abortion, Bleeding or any abnormal cases . 5- No specific or Unauthorized drug is used during pregnancy 6- primiparous pregnancy 7- normal fetus-baby weigh less than 4000 grams by using Johnson's formula [W=( -N 155], Fundal height (cm) above the pubic symphysis minus 12 if Vertex above Ischial Spine or minus 11 if below Ischial Spines. 8- no history of infertility 9- normal pelvis diameters (based on vaginal examination),height should not be under 145cm 10- absence of mental illness or any other disorder that makes her unable to communicate(deafness – blindness) 11- Interesting to participate in research study Exclusion criteria 1- maternal-fetal emergency intervention is required (Bleeding, like placental abruption, emergency cesarean for any reason) during labor 2- withdraw from the partnership

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Neonatal outcomes: Apgar scor. Timepoint: After intervention. Method of measurement: Cheklist/ examination/ observation.;Neonatal outcomes:ABG. Timepoint: After intervention. Method of measurement: Cheklist/ examination/ observation.;Neonatal outcomes: NICU. Timepoint: After intrevention. Method of measurement: Cheklist/ examination/ observation.;Maternal outcomes: Post partum infection. Timepoint: After intervention. Method of measurement: Cheklist/ examination/ observation.;Average lenghth of the second Stage of labor. Timepoint: Lenghth of intervention. Method of measurement: Partograph.;Average lenghth of the third stage of labor. Timepoint: Lenghth of intervention. Method of measurement: Partograph.;Maternal outcomes: Type of delivery. Timepoint: One month after intervention. Method of measurement: Cheklist/ examination/ observation.;Average lenghth of the first stage of labor. Timepoint: Lenghth of intervention. Method of measurement: Partograph.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026