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Incision Pain and Uterine Contraction Pain After Cesarean Section

NCT02595333 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2015-11-03

No results posted yet for this study

Summary

This study aims to compare the pain degree between primary cesarean section and repeated cesarean section, and investigate the role of flurbiprofen axetil in postoperative analgesia, so as to provide reference for clinical practice.

Conditions

  • C.Delivery; Surgery (Previous), Gynecological

Interventions

DRUG

Group SF1

primary cesarean section+postoperative analgesia with sufentanil plus flurbiprofen axetil group

DRUG

Group S1

sufentanil was administered for analgesia in primary cesarean section

DRUG

Group SF2

sufentanil and flurbiprofen was administered for analgesia in repeated cesarean section

DRUG

Group S2

sufentanil was administered for analgesia in repeated cesarean section

Sponsors & Collaborators

  • Fudan University

    lead OTHER

Principal Investigators

  • Shaoqiang Huang · Department of Anesthesiology, Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-11-30
Primary Completion
2017-08-31
Completion
2017-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02595333 on ClinicalTrials.gov