CTRI/2022/08/044631
Not yet recruiting
未知
A Randomized Controlled study to compare the dose requirement of Oxytocin for management of uterine atony in patients receiving prophylactic Phenylephrine during Cesarean Delivery
College of Medicine and Sagore Dutta Hospital Kamarhati Kolkata0 sites0 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: O746- Other complications of spinal andepidural anesthesia during labor and delivery
- Sponsor
- College of Medicine and Sagore Dutta Hospital Kamarhati Kolkata
- Status
- Not yet recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •a. single pregnancy at full\-term (gestational age ââ?°Â¥37 weeks)
- •b. American Society of Anesthesiologists Physical Status I and II
- •c. aged between 20 and 35 years old undergoing caesarean section
Exclusion Criteria
- •a. obesity (body mass index, BMI \>35 kg/m2\),
- •b. height ( \<150 or \>170 cm),
- •c. active labor/ early labor
- •d. diabetes mellitus or gestational diabetes
- •e. hypertension or pre\-eclampsia
- •f. intrauterine growth restriction or fetal macrosomia
- •g. placenta previa, placenta conglutination, placenta implantation
- •h. significant co\-existing maternal disease
- •i. any absolute contraindications to spinal anesthesia such as local infection or bleeding disorders, and cases with a sensory plane block that did not reach T6 or higher.
Outcomes
Primary Outcomes
Not specified
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