Clinical Trials Directory

Trials / Unknown

UnknownNCT03433976

Prilocaine or Bupivacaine for Spinal Anesthesiain Pregnant

Comparison of the Duration of Motor Block After Spinal Anesthesia for Planned Cesarean Sections: Hyperbaric Prilocaïne Versus Hyperbaric Bupivacaine

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
University Hospital, Montpellier · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The planned cesarean section is an intervention with a standard operating time of less than 40 minutes in trained teams. Hyperbaric Bupivacaine is the local anesthetic (LA) reference for these operations. But the duration of its motor block is generally greater than 3 hours. The purpose of this study is to show a reduction in motor block time with hyperbaric Prilocaine by at least 30 minutes, which would allow mothers and their children to return to the maternity ward earlier and thus improve the circulation of patients within the maternity's PACU.

Detailed description

Prospective study, randomized into two parallel groups (Hyperbaric Prilocaïne versus hyperbaric Bupivacaine), double-blind, monocentric (Clinique Saint Roch in Montpellier). The number of subjects required is 50 patients, 25 per group.

Conditions

Interventions

TypeNameDescription
DRUGspinal anesthesiaspinal anesthesia for planned cesarean sections

Timeline

Start date
2018-05-07
Primary completion
2020-05-07
Completion
2020-08-30
First posted
2018-02-15
Last updated
2018-12-11

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT03433976. Inclusion in this directory is not an endorsement.