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Comparison the effect of lavender and Nitrous oxide on labor pai

Phase 3
Conditions
Pain.
Pain, not elsewhere classified
Registration Number
IRCT20180610040032N1
Lead Sponsor
Bojnourd University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
72
Inclusion Criteria

Gestational age Between 37 and 42 weeks
At least Diploma Literacy
Singleton pregnancy
4 cm dilatation
Low risk pregnancy (no rupture over 6 hours of water sac)
Conscious consent of the individual to enter the study

Exclusion Criteria

Preterm delivery
Third-trimester hemorrhage and intrauterine growth retardation
Preeclampsia
24History of acute and chronic pain such as migraine
Performing professional exercise (due to changes in the threshold of pain and delivery phase)
Drug Addiction, Alcohol and Smoking
Receive analgesic within 3 hours before the onset of intervention
History of allergy to herbal
Diseases of internal and surgical diseases in mother and fetus
Existence of fetal distress symptoms
Clear stenosis in the pelvic floor
Known mental disease
Stay in active phase of labor
Diabetes
Seizure

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in pain. Timepoint: Before the beginning of the study, at dilates 6-4, 8-6, 10-8 cm and immediately after intervention. Method of measurement: VAS.
Secondary Outcome Measures
NameTimeMethod
Satisfaction Survey. Timepoint: End of research. Method of measurement: questionnaire.
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