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Clinical Trials/EUCTR2008-006235-12-IT
EUCTR2008-006235-12-ITActive, not recruitingNot Applicable

INTRATHECAL LEVOBUPIVACAINE USE IN CESAREAN SECTION : DETERMINATION OF ?MINIMUM LOCAL ANESTHETIC DOSE (MLAD)? - ND

AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI0 sitesStarted: July 22, 2009Last updated:
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Conditions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Sponsor
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional clinical trial of medicinal product

Eligibility Criteria

Sex
Female

Inclusion Criteria

  • •Gathering of informed consent; ASA 1-2; Age between 18 and 44 years Maternal height between 150 and 190 cm, Maternal weight between 50 and 120 kg, Women who underwent elective or scheduled cesarean section.
  • •Are the trial subjects under 18? no
  • •Number of subjects for this age range:
  • •F.1.2 Adults (18-64 years) yes
  • •F.1.2.1 Number of subjects for this age range
  • •F.1.3 Elderly (>=65 years) no
  • •F.1.3.1 Number of subjects for this age range

Exclusion Criteria

  • •Obstetrical complications associated with a higher hemorrhagic risk (e.g. central placenta praevia), Twin or multiple pregnancies, Inherited or acquired coagulation disorders, Skin infections or previous/actual spinal disorders, ASA >2, Urgent cesarean section, Severe clinical conditions that do not allow the enrollment of the patient, Use of experimental drugs within months before the inclusion in the study

Investigators

Sponsor
AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI

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