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Clinical Trials/IRCT2012100811020N2
IRCT2012100811020N2Completed未知

Comparison of Incremental Bolus and Infusion Administration of Remifentanil on Labor Pain and Length of Delivery Time in Women During Labor.

Zahedan University of Medical Sciences, Deputy of Research0 sites82 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
82

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 years to 35 years (—)
Sex
Female

Inclusion Criteria

  • primigravid healthy parturient with 37-42 weeks of pregnancy; in active stage of labor (uterine contraction 3 per 10 minutes, lasting for 30 to 40 seconds and cervical dilation >=3 cm); with vertex presentation. Exclusion criteria: parturient with positive history of preeclampsia; using psychiatric drugs; using opioid and alcohol; antenatal hemorrhage; fetal distress; BMI>30 or <20; multi tone and requesting for epidural analgesia.

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Zahedan University of Medical Sciences, Deputy of Research

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