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Painless vaginal delivery

Intravenous paracetamol versus intramuscular pethidine in relief of labor pain in primigravid women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201207215506N5
Enrollment
80
Registered
2012-09-24
Start date
2012-02-20
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

vaginal delivery with vertex presentation. Spontaneous vertex delivery

Interventions

Intervention 1: Since beginning of active phase of delivery (50 mm of cervical dilatation and 100 % effacement), patients in group control received 50mg intramuscular pethedine injection. Interventio
Treatment - Drugs
Since beginning of active phase of delivery (50 mm of cervical dilatation and 100 % effacement), patients in group control received 50mg intramuscular pethedine injection.
Intervention group: Since beginning of active phase of delivery (50 mm of cervical dilatation and 100 % effacement), patients in this group received an intravenous solution infusion containing 1000mg

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: inclusion criteria: primigravid singleton women with fullterm pregnancy (gestational age more than 37 weeks based on ultrasound findings) candidated for normal vaginal delivery exclusion criteria:were history of cardiac, liver and renal disease, anti-convulsive medication consumption, malpresentation of fetus, abnormal fetal monitoring during labor and multiple gestations

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Labor pain. Timepoint: Immediately after child birth. Method of measurement: Visual analogue scale.

Secondary

MeasureTime frame
Neonatal Apgar score. Timepoint: Immediately and 5 minutes after child birth. Method of measurement: Apgar score table.;Medical complication. Timepoint: 24 hours after delivery. Method of measurement: Study questionarie.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mohammad Hassan Abdollahi

Yazd University of Medical Sciences

mhabdollahi@yahoo.co.uk; mhabdollahi@ssu.ac.ir+98 35 1826 0277

Outcome results

None listed

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