Epidural Analgesia in Different Cervix Diameter and the Rate of Cesarean Delivery

NCT00677274 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 780

Last updated 2009-02-12

No results posted yet for this study

Summary

Epidural analgesia in the early stage of labor at cervix \< 4.0cm was considered as a risk period for increasing the rate of cesarean delivery. The more recent studies and the investigators' previous data indicated epidural analgesia can be performed as early as the cervical dilation approximately 2.0cm. The investigators hypothesized that different cervix diameter had different rate of cesarean delivery. This trial would investigate the correlation amongst different cervical dilation and the risk of cesarean section in nulliparous women at term.

Conditions

  • Labor Pain

Interventions

PROCEDURE

Epidural labor analgesia

Epidural analgesia initiated at the onset of regular uterine contraction

PROCEDURE

Epidural labor analgesia

Epidural analgesia initiated at the cervix diameter 0.5cm

PROCEDURE

Epidural labor analgesia

Epidural analgesia initiated at the cervix diameter 1.0cm

PROCEDURE

Epidural labor analgesia

Epidural analgesia initiated at the cervix diameter 1.5cm

PROCEDURE

Epidural labor analgesia

Epidural analgesia initiated at the cervix diameter 2.0cm

PROCEDURE

Epidural labor analgesia

Epidural analgesia initiated at the cervix diameter 3.0cm

PROCEDURE

Epidural labor analgesia

Epidural analgesia initiated at the cervix diameter 4.0cm

PROCEDURE

Epidural labor analgesia

Epidural analgesia initiated at the cervix diameter 5.0cm

Sponsors & Collaborators

  • HRSA/Maternal and Child Health Bureau

    collaborator FED
  • Nanjing Medical University

    lead OTHER

Principal Investigators

  • XiaoFeng Shen, MD · Nanjing Medical University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-05-31
Primary Completion
2008-08-31
Completion
2008-08-31

Countries

  • China

Study Locations

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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 NCT00677274 on ClinicalTrials.gov