Evaluation of the effect of paracetamol with Entonox in comparison with pethidine with Entonox on labor pai
Phase 3
Recruiting
- Conditions
- Pain during labor.
- Registration Number
- IRCT20220116053734N1
- Lead Sponsor
- Qazvin University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
Patients should be between 18 and 45 years old.
The fetal presentation should be cephalic.
Fetuses are single.
Dilatation of the uterus should be 4 cm.
Exclusion Criteria
Having a fetal growth disorder
Having a history of chronic pain
Having an addiction to drugs, alcohol and smoking
Having indications for cesarean section
Havind a history of severe psychological disorders, cardiovascular, renal, respiratory, asthma, diabetes, hypertension, coagulation disorders and epilepsy in mother
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method abor pain score. Timepoint: before drug injection and 15, 30, 45, 60 and 120 minutes after drug injection. Method of measurement: pain NRS numerical rating scale.
- Secondary Outcome Measures
Name Time Method The time between drug injection and delivery. Timepoint: Drug injection time and fetus delivery time. Method of measurement: time.;Placenta delivery time. Timepoint: delivery time and placenta delivery time. Method of measurement: time.;Newborn Apgar score. Timepoint: 1 and 5 minutes after labor. Method of measurement: Apgar score.;Mother hemoglobin level. Timepoint: Before delivery and 6 hours after delivery. Method of measurement: Hemoglobin.;Drug side effects in the mother including headache/dizziness/blurred vision/dry mouth/nausea/vomiting/dyspnea. Timepoint: During the time of drug injection until delivery. Method of measurement: Ask the patient.