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Clinical Trials/RBR-4hsyy4
RBR-4hsyy4
Completed
Phase 3

abor Analgesia: Comparison between low doses of Pethidine and Sodium Dipyrone

IFOR - Universidade de Fortaleza0 sitesJanuary 4, 2018

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Pain, Maternal Suffering during labor, women
Sponsor
IFOR - Universidade de Fortaleza
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 4, 2018
End Date
TBD
Last Updated
2 years ago
Study Type
Intervention
Sex
Female

Investigators

Sponsor
IFOR - Universidade de Fortaleza

Eligibility Criteria

Inclusion Criteria

  • Presence of at least 3 uterine contractions lasting 40 seconds or more every 10 minutes; Patients presenting a dilation of the uterine cervix equal to or greater than 5 cm; Measurement of pain through the use of visual analogue scale equal to or greater than 8; Gestational age of 37 up to 40 weeks and 6 days; Fetuses in cephalic presentation

Exclusion Criteria

  • Parturients with any of the following events: poorly controlled arterial hypertension, diabetes, restricted intrauterine growth and placental abruption; Use of oxitocyn by pregnant women in the period from the begining of labor until 2 hours after administration of the analgesic; Hypothyroidism diagnosed previously and without therapy; Patients taking monoamine oxidase inhibitors; Occurrence of labor less than 1 hour after analgesia; Parturients with body mass greater than 100 kg; Indication of cesarean delivery during admission; Addison's disease previously diagnosed; BCF's \< 110 bpm, during admission; BCF's \> 160 bpm, during admission; Patients allergic to sodium dipyrone; Patients allergic to pethidine; Users of chlorpromazine; Phenobarbital users; Phenytoin users; Fetus without vilality; Twin pregnancy; Drug addiction

Outcomes

Primary Outcomes

Not specified

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