A Clinical Trial to Determine the Effects of Upright Position on Labour Outcomes.
Not Applicable
Completed
- Conditions
- Health Condition 1: O94- Sequelae of complication of pregnancy, childbirth, and the puerperium
- Registration Number
- CTRI/2022/04/041740
- Lead Sponsor
- il
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
Pregnant women in their 1st stage of labour.
Pregnant women who are in a natural process.
Pregnant women with single live fetus in cephalic presentation.
Exclusion Criteria
Women with complicated pregnancy .
Women who are contraindicated for NVD.
Any abnormal condition of fetus.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of labourTimepoint: Active Stage of Labour when Mother are at Full Term.
- Secondary Outcome Measures
Name Time Method General Health of Mother. <br/ ><br>General Health of the Baby. <br/ ><br>Perineal Laceration/Trauma.Timepoint: Active Stage of Labour when Mother are at Full Term.
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms explain upright positioning's impact on labor outcomes in O94 complications?
How does upright labor positioning compare to standard-of-care for maternal and fetal outcomes in puerperium complications?
Are there biomarkers that predict response to upright positioning in selected labor outcomes among pregnant women?
What are the potential adverse events associated with upright positioning during labor and how are they managed?
What combination approaches or alternative therapies are being explored alongside upright positioning for improving labor outcomes in O94 conditions?