Status:

COMPLETED

Determination of Sufentanil in Breast Milk of Puerpera

Lead Sponsor:

Fujian Medical University Union Hospital

Conditions:

Cesarean Section

Eligibility:

FEMALE

20-38 years

Phase:

PHASE4

Brief Summary

To determination of sufentanil in human breast milk during the administration of the sufentanil via the analgesic infusion pump and after the administration, to determine whether the breastfeeding aft...

Detailed Description

The concentration of sufentanil in milk was determined by LC-MS /MS method( liquid chromatography mass spectrometry).The separation was carried on Agilent ZORBAX Eclipse Plus C18 column(2.1×50 mm, 3.5...

Eligibility Criteria

Inclusion

  • Aged 20yr to 38yr
  • Height 155\~170 cm
  • Weight 65\~85 Kg
  • American Society of Anesthesiologists statuses I or II
  • Normal cardiac and pulmonary function
  • Undergoing elective Cesarean section
  • Willing to provide breast milk

Exclusion

  • pregnancy induced hypertension
  • gestational diabetes
  • gestational heart disease

Key Trial Info

Start Date :

August 1 2015

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 1 2017

Estimated Enrollment :

100 Patients enrolled

Trial Details

Trial ID

NCT03764202

Start Date

August 1 2015

End Date

December 1 2017

Last Update

December 5 2018

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