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Effect of intramuscular administration of Dexamethasone on the induction of labor and duration of labor and its complications

Effect of intramuscular administration of Dexamethasone on the induction of labor and duration of labor and its complications

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201401221760N29
Enrollment
120
Registered
2014-03-13
Start date
2014-03-09
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

Condition 1: induction of labor. Condition 2: duration of labor. Preterm labour and delivery Preterm labour and delivery

Interventions

Intervention 1: Intervention groups: dexamethasone sodium phosphate (2cc) (from Caspian) is injected. After 6 h induction begins.If you do not enter an active phase (3 contractions in 10 minutes with
Treatment - Drugs
Intervention groups: dexamethasone sodium phosphate (2cc) (from Caspian) is injected. After 6 h induction begins.If you do not enter an active phase (3 contractions in 10 minutes with regular dilata
Control group: Sterile water injections (2cc)

Sponsors

Vice Chancellor for Research and Technology, Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
16 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Pregnant women with a gestational age of 38 weeks or more; Bishop score greater than or equal to 7; Singleton pregnancy, cephalic; Normal embryo sac. Exclusion criteria: Abnormal vaginal bleeding (risk of placenta previa or placental abruption); History of any systemic diseases (HTN, DM, etc); Receiving any medical treatment except for routine supplementation in pregnancy; Suspected macrosomia (ultrasound or clinical assessment by a skilled person); Excessive uterine distension (polyhydroamnious evidence); presentation non-cephalic; Active phase of labor (cervical dilatation 2-3 cm4-3 with a strong contraction in width, 10); PROM; IUGR10; Fetal distress, bad hips; Any uterine abnormalities or any uterine surgery, including Cesarean delivery on admission;

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Reducing the time between the onset of the active phase of labor induction. Timepoint: 6 hours after injection of dexamethasone and induction. Method of measurement: Clinical.;Reduce the duration of the active phase of labor. Timepoint: 38 weeks to 42 weeks of gestation. Method of measurement: Clinical.;Reduction stage II of labor. Timepoint: Dilatation and expulsion of fetus. Method of measurement: Clinical.

Secondary

MeasureTime frame
Apgar scores after birth. Timepoint: In the first minutes after birth. Method of measurement: Clinical.;Baby Weight. Timepoint: Birth. Method of measurement: Kg.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Zeinab Pahlavan

Fatemehzahra Fertility & reproductive Health Research Center

a.uosefnezhad@gmail.com+98 11 1227 4881

Outcome results

None listed

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