Evaluation of intrathecal dexamethasone and sufentanil in natural vaginal delivery
Phase 3
Recruiting
- Conditions
- abour pain.Encounter for full-term uncomplicated delivery
- Registration Number
- IRCT20220419054587N1
- Lead Sponsor
- Karaj University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
Age between 20-35 year
Exclusion Criteria
Multiples
Underlying disease
Drug history
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of analgesia. Timepoint: From intervention to the end of labor. Method of measurement: The first request for repeated analgesia by the mother.;Labour phase. Timepoint: From intervention to the end of labour. Method of measurement: Serial examination to check the course of labour.
- Secondary Outcome Measures
Name Time Method