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Clinical Trials/PACTR201710002424167
PACTR201710002424167
Completed
未知

Maternal and fetal outcomes in three regimens for intrathecal analgesia in multipara women undergoing normal vaginal delivery

Faculty of Medicine0 sites100 target enrollmentJuly 13, 2017
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ConditionsPregnancy and Childbirthpan free normal vaginal delivery

Overview

Phase
未知
Intervention
Not specified
Conditions
Pregnancy and Childbirth
Sponsor
Faculty of Medicine
Enrollment
100
Status
Completed
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 13, 2017
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Faculty of Medicine

Eligibility Criteria

Inclusion Criteria

  • •Multipara woman, ASA physical status I or II,
  • •in active labor with engaged fetal head, term pregnancy of singleton fetus not in distress (Normal cardiotocography \[baseline fetal heart rate between 110 and 160 beats/minute, baseline variability \>5 beats/minute, presence of accelerations, and absence of decelerations],
  • •minimal cervical dilatation of at least 3 cm with intact membranes,
  • •those requiring oxytocin augmentation, cephalic presentation, and uncomplicated pregnancies.

Exclusion Criteria

  • •Patients who refuse to participate, preexisting or pregnancy\-induced hypertension,
  • •endocrine diseases,
  • •diagnosed fetal abnormalities,
  • •contra\-indications to neuraxial anesthesia, occurrence of wet tap during epidural placement,
  • •fade of spinal analgesia \& hence need for epidural activation,
  • •previous systemic opioid administrations, allergy to study agents,
  • •unconscious parturients,
  • •patients who are unable to communicate.

Outcomes

Primary Outcomes

Not specified

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