Status:

COMPLETED

Intravenous Remifentanil for Labor Analgesia

Lead Sponsor:

Nanjing Medical University

Collaborating Sponsors:

HRSA/Maternal and Child Health Bureau

Conditions:

Labor Pain

Eligibility:

FEMALE

18-45 years

Phase:

PHASE4

Brief Summary

Labor analgesia is an essential health caring procedure for women. However, epidural analgesia cannot be performed on all subjects for different contraindications, such as lower platelet counter, back...

Eligibility Criteria

Inclusion

  • Nulliparous women
  • \> 18 years and \< 45 years
  • Spontaneous labor
  • Analgesia request
  • Epidural puncture contraindications
  • Tendency of bleeding

Exclusion

  • Allergy to opioids, a history of the use of centrally-acting drugs of any sort, chronic pain and psychiatric diseases records
  • Participants younger than 18 years or older than 45 years
  • Those who were not willing to or could not finish the whole study at any time
  • Using or used in the past 14 days of the monoamine oxidase inhibitors
  • Alcohol addictive or narcotic dependent patients were excluded for their influence on the analgesic efficacy of the epidural analgesics
  • Subjects with a nonvertex presentation or scheduled induction of labor
  • Cervical dilation was 5.0cm or greater before performing epidural puncture and catheterization
  • Diagnosed diabetes mellitus and pregnancy-induced hypertension
  • Twin gestation and breech presentation

Key Trial Info

Start Date :

July 1 2008

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

September 1 2009

Estimated Enrollment :

1000 Patients enrolled

Trial Details

Trial ID

NCT00710086

Start Date

July 1 2008

End Date

September 1 2009

Last Update

September 18 2009

Active Locations (1)

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Nanjing Maternal and Child Health Care Hospital

Nanjing, Jiangsu, China, 210004