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Spinal Analgesia Versus No Analgesia: Study for External Cephalic Version

NCT00119184 · Status: TERMINATED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 140

Last updated 2017-11-28

No results posted yet for this study

Summary

The purpose of this study is to examine whether spinal anesthesia affects the chances of successful external cephalic version (ECV) of a breech presenting fetus.

Two study groups will be included; one will receive spinal anesthesia, the other will not. The non-spinal group will be permitted to cross over if ECV procedure is painful.

The main outcome is success of ECV.

Conditions

  • Breech Presentation

Interventions

PROCEDURE

External cephalic version

7.5 mg bupivacaine intrathecally

DRUG

spinal anesthesia

spinal anesthesia

Sponsors & Collaborators

  • Hadassah Medical Organization

    lead OTHER

Principal Investigators

  • Carolyn F Weiniger, MB ChB · Dept Anesthesiology, Hadassah Hebrew University Medical School

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2002-10-31
Primary Completion
2006-03-31
Completion
2008-05-31

Countries

  • Israel

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 NCT00119184 on ClinicalTrials.gov