CTRI/2022/01/039343Not yet recruiting未知
Prophylactic Phenylephrine and Norepinephrine infusions during Caesarean Delivery for non-reassuring fetal heart rate: A randomised non-inferiority trial to assess neonatal outcome
POSTGRADUATE INSTITUTE OF MEDICAL EDUCATION AND RESEARCH CHANDIGARH0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- 未知
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1. ASA physical status II.
- •2. Women with category I fetal heart trace at the
- •beginning of labor and later on showed a change
- •to category II trace with/without improvement
- •following intrauterine fetal resuscitation
- •3. Fetal growth restriction (FGR) requiring
- •emergency CD was included if the subject was
- •near-term pregnancy with fetal biophysical
- •profile more than 6 before induction of labor
- •and later on showed category II trace with
- •normal fetal doppler flows.
- •4. Women with Category II FHR tracings
Exclusion Criteria
- •1. Refusal to give informed consent.
- •2. Age <18yrs.
- •3. Allergy to phenylephrine and norepinephrine.
- •4. Contraindication for SA.
- •5. Known fetal abnormality.
- •6. Cardiovascular or cerebrovascular diseases.
- •7. Any autoimmune disorder.
- •8. Hypertensive disorder of pregnancy.
- •9. Diabetes mellitus.
- •10. Multiple gestation.
- •11. Growth restricted fetus having chronic
- •asphyxia (previous abnormal nonstress test
- •and biophysical profile less than 6).
- •12. Ruptured membranes with meconium-stained
- •liquor, or evidence of intrauterine infection.
Investigators
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