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The effect of progesterpne supp.200mg on prevention of preterm labor after inhibition of uterine contraction in patients of Shariaty Hospital of Banddar Abbas 2014-2015

The effect of progesterpne supp.200mg on prevention of preterm labor after inhibition of uterine contraction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016082229485N1
Enrollment
200
Registered
2016-09-17
Start date
2016-04-28
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

Preterm labour. Preterm labour without delivery

Interventions

Intervention 1: Intervention group 1: The treatment group received a weekly intramuscular injection of vaginal progesterone suppositories 200 mg . They were advised to continue it until their 36th we
Treatment - Drugs
Intervention group 1: The treatment group received a weekly intramuscular injection of vaginal progesterone suppositories 200 mg . They were advised to continue it until their 36th week of pregnancy
control group: The control group would receive no such injection.

Sponsors

Vice Chancellor for research of Hormozgan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: Between 26-34 weeks pregnancy age; There premature uterine contractions. Exclusion criteria: the pregnancy age above 34 weeks (since in this group there would be no reason for preventing uterine contractions due to the fetal lung maturation); preterm rupture of membranes; corioamnionite, blood loss prior to the labor due to placental abruption or previa;multiple pregnancies; concomitant systemic diseases (preeclampsia, gestational diabetes (GDM); cardiovascular diseases; kidney diseases; asthma; hyperthyroid; …).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The prevention of preterm birth after inhibition of uterine contractions. Timepoint: 48 hours after the intervention. Method of measurement: Check up and examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoumeh Darijani

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mdri18@yahoo.com+98 76 3333 2424

Outcome results

None listed

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