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Clinical Trials/NCT03333902
NCT03333902
Completed
Not Applicable

The Comparison Of Different Nerve Blocks For Postoperative Analgesia In Cesarean Delivery: A Randomized Controlled Trial

Feng Xia1 site in 1 country102 target enrollmentDecember 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anesthesia, Obstetrical
Sponsor
Feng Xia
Enrollment
102
Locations
1
Primary Endpoint
the change trend of Visual Analogue Scale (VAS) at rest and movement
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The purpose of this study is to investigate the effect of different kinds of popular peripheral nerve blocks for postoperative analgesia after cesarean delivery is completed, compared with traditional epidual analgesia.

Detailed Description

Visual Analogue Scale (VAS) and morphine consumption was adopted to evaluate the pain relief.

Registry
clinicaltrials.gov
Start Date
December 1, 2017
End Date
August 30, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Feng Xia
Responsible Party
Sponsor Investigator
Principal Investigator

Feng Xia

Professor

First Affiliated Hospital, Sun Yat-Sen University

Eligibility Criteria

Inclusion Criteria

  • American Society of Anesthesiologists (ASA) physical status I or II
  • weight from 50 to 70 kilogrammes
  • a normal singleton pregnancy
  • ≥37 weeks gestation

Exclusion Criteria

  • congenital coagulopathy
  • anatomic abnormalities
  • localized skin infection
  • allergy to any of the drugs used

Outcomes

Primary Outcomes

the change trend of Visual Analogue Scale (VAS) at rest and movement

Time Frame: 0-48 hours postoperatively

The purpose is to view the change of the level of pain assessed by subjects at adjacent time points. We would set 0, 4, 6, 12, 24, 48 hours postoperatively as observational time points.

Secondary Outcomes

  • total morphine consumption(0-48 hours postoperatively)
  • complications(0-48 hours postoperatively)

Study Sites (1)

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