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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.
Investigators
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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