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Clinical Trials/NCT02710877
NCT02710877
Terminated
Not Applicable

Pain Management During Labor: Use of Intermittent Drug Delivery Devices for Obstetric and Neonatal Outcome Improvement and Health-care Burden Reduction

University of Modena and Reggio Emilia3 sites in 1 country671 target enrollmentDecember 23, 2014

Overview

Phase
Not Applicable
Intervention
Programmed Intermittent bolus
Conditions
Labor Pain
Sponsor
University of Modena and Reggio Emilia
Enrollment
671
Locations
3
Primary Endpoint
Rate of instrumental delivery
Status
Terminated
Last Updated
8 years ago

Overview

Brief Summary

The study aims to determine whether the use of automated intermittent devices for labor analgesia could prevent the increase of instrumental deliveries, with same analgesia.

Moreover it will evaluate if automated devices can allow a reduction of health-care burden.

Detailed Description

Epidural analgesia is recognized as the most effective technique to control labor pain, although its possible adverse events. Continuous epidural administration of local anesthetics can stabilize the analgesic block and reduce the anesthesiologists' workload but is associated with an increase in operative vaginal delivery. Epidural intermittent boluses performed by anesthetist are associated to reduction of dosages, but they could provide insufficient analgesia and they involve the constant anesthetist's presence in the operating room. This is a multicenter randomized controlled trial with two arms, funded by grant of Regione Emilia Romagna, in which we will compare two different epidural analgesia protocols: anesthesiologist's supervised versus intermittent boluses with PCEA.

Registry
clinicaltrials.gov
Start Date
December 23, 2014
End Date
February 28, 2018
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
University of Modena and Reggio Emilia
Responsible Party
Principal Investigator
Principal Investigator

Laura Rinaldi

Medical Doctor

University of Modena and Reggio Emilia

Eligibility Criteria

Inclusion Criteria

  • Nulliparous women at full-term pregnancy single fetus and vertex presentation, hospitalized for harbingers of labor and cervical dilation less than 5 cm
  • Numeric Rate Scale \> 5

Exclusion Criteria

  • patients aged under 18 years
  • patients with ongoing administration of oxytocin
  • patients with no indications to epidural analgesia
  • patients with inability to place the epidural catheter for technical difficulty
  • patients with parenteral administration of opioids
  • multiparous women
  • patients unable to understand the objectives and procedures of the study

Arms & Interventions

Programmed Intermittent bolus (PIEB)

Intervention: epidural analgesia through administration of a mixture of levobupivacaine 0,0625% and sufentanil 4 mcg. Intermittent bolus of 10 ml mixture every 75 minutes. Patient controlled bolus of 5 ml same mixture, lock-out 15 minutes.

Intervention: Programmed Intermittent bolus

Programmed Intermittent bolus (PIEB)

Intervention: epidural analgesia through administration of a mixture of levobupivacaine 0,0625% and sufentanil 4 mcg. Intermittent bolus of 10 ml mixture every 75 minutes. Patient controlled bolus of 5 ml same mixture, lock-out 15 minutes.

Intervention: Levobupivacaine

Programmed Intermittent bolus (PIEB)

Intervention: epidural analgesia through administration of a mixture of levobupivacaine 0,0625% and sufentanil 4 mcg. Intermittent bolus of 10 ml mixture every 75 minutes. Patient controlled bolus of 5 ml same mixture, lock-out 15 minutes.

Intervention: Sufentanil 4 mcg

Manuale epidural bolus (TOP-UP)

Intervention: manual epidural bolus of 15 ml levobupivacaine 0,0625% and sufentanil 5 mcg on maternal request.

Intervention: Manual epidural bolus

Manuale epidural bolus (TOP-UP)

Intervention: manual epidural bolus of 15 ml levobupivacaine 0,0625% and sufentanil 5 mcg on maternal request.

Intervention: Levobupivacaine

Manuale epidural bolus (TOP-UP)

Intervention: manual epidural bolus of 15 ml levobupivacaine 0,0625% and sufentanil 5 mcg on maternal request.

Intervention: Sufentanil 5 mcg

Outcomes

Primary Outcomes

Rate of instrumental delivery

Time Frame: Through labor completion

Vaginal delivery obtained through vacuum device intervention decided independently by the obstetrician on duty, according to defined local protocols and according to the conditions of the mother and fetus.

Secondary Outcomes

  • Adequate analgesia(Labor length since peridural catheter insertion until delivery)
  • Time-related amount of local anesthetic(Labor length since peridural catheter insertion until delivery)
  • Motor block episodes(Labor length since peridural catheter insertion until delivery)
  • Health economic assessment(Labor length since peridural catheter insertion until delivery)
  • Anesthesiologist working time(Labor length since peridural catheter insertion until delivery)
  • Total amount of local anesthetic(Labor length since peridural catheter insertion until delivery)

Study Sites (3)

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