Evaluation of the effects of Entonox and local anesthesia in painless delivery
Phase 3
- Conditions
- Painless delivery.
- Registration Number
- IRCT20201219049769N1
- Lead Sponsor
- Islamic Azad University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
Single term pregnancy
Cephalic presentation
No problem in decending of fetus
Exclusion Criteria
Asthma
Hypertension
Diabetes Melitus
Fetal distres and death
Massive vaginal bleeding
Placenta previa
Infection in sight of injection
Coagulopathy
Severe headache
Dyspnea
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Analgesic rate based on Visual Analogue Scale. Timepoint: Group A once before inhalation of Entonox and once after 4 inhalations and group B before anesthesia and 5 minutes after anesthesia. Method of measurement: Visual Analogue Scale will be used to measure pain.
- Secondary Outcome Measures
Name Time Method