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Clinical Trials/CTRI/2022/08/044631
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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional

Investigators

Sponsor
College of Medicine and Sagore Dutta Hospital Kamarhati Kolkata

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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