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The effect of acetaminophen and pethidine on reducing the pain of the first stage of labor and its complications in primipara women

Comparison of the effectiveness of acetaminophen and pethidine in the first stage of labor on reducing the pain and maternal complications of primigravid women

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190202042595N1
Enrollment
100
Registered
2019-02-13
Start date
2018-12-24
Completion date
Unknown
Last updated
2019-02-25

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: First Intervention group: Acetaminophen receptor, 100 mg of acetaminophen in 100 cc serum ringer lactate within 15 minutes. Intervention 2: Second Intervention group: Pethidine, 50 mg

Sponsors

Rafsanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Single with cephalic presentation Pregnant women requesting a reduction in labor pain

Exclusion criteria

Exclusion criteria: Underlying disease(cardiac, hepatic, renal, pulmonary) Preeclampsia Diabetes Drug abuse Sensitization to acetaminophen and opioids G6PD deficiency Cesarean section history

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before drug administration, 30 minutes, 1, 2, 3 and 4 hours after drug administration. Method of measurement: Visual analog scale(VAS) by graded ruler (0 to 10), which zero is painless and 10 most severe pain states.;Maternal complications. Timepoint: From the time of drug injection to 4 hours after delivery. Method of measurement: Nausea, vomiting, drowsiness, respiratory depression.;Duration of the first stage of labor. Timepoint: Distilation time of 4 cm to complete dilatation. Method of measurement: minute.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoume Khammar

Rafsanjan University of Medical Sciences

masoume.khammar@rums.ac.ir+98 34 3425 5900

Outcome results

None listed

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