FETO-MATERNAL OUTCOME IN INSTRUMENTAL VAGINAL DELIVERY-A CROSS SECTIONAL STUDY
Not Applicable
- Conditions
- Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
- Registration Number
- CTRI/2021/09/036639
- Lead Sponsor
- Melmaruvathur adhiparashakthi institute of medical sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)Age at delivery 18 to 35 years
2)Singleton term pregnancy
3)Cephalic presentation
4)Absent membranes
5) Clinically adequate pelvis
6)Average size baby (2-3.5 kg)
Exclusion Criteria
1)Intrauterine fetal death
2)Multiple gestation
3)Gross congenital anomalous fetus
4) Contracted pelvis /cephalopelvic disproportion
5)High station above +3
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method MATERNAL OUTCOME:1)episiotomy extensions <br/ ><br>2)maternal injuries-vaginal/cervical lacerations <br/ ><br>-third and fourth degree perineal tear <br/ ><br>-parauretheral tear <br/ ><br>-vulvo vaginal haematoma <br/ ><br>FETAL OUTCOME :Resuscitation if any:1)Tactile stimulation <br/ ><br> 2)Ambu bag <br/ ><br> 3)Intubation <br/ ><br>Complications if any:1)Respiratory distress <br/ ><br> <br/ ><br>2)scalp and facial marks and bruises <br/ ><br>3)facial palsy <br/ ><br>4)Cephalhaematoma <br/ ><br> <br/ ><br>Timepoint: Primary outcome - during at the time of delivery
- Secondary Outcome Measures
Name Time Method Post delivery-Baby mother side /NICU admissionTimepoint: Secondary outcome- monitoring 24 hours post delivery