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
| Type | Name | Description |
|---|---|---|
| DRUG | spinal anesthesia | spinal 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.