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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
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03433976
Acronym
Césarcaïne
Enrollment
50
Registered
2018-02-15
Start date
2018-05-07
Completion date
2020-08-30
Last updated
2018-12-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cesarean

Keywords

Caesarean section, spinal anesthesia, Prilocaïne, motor block

Brief 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.

Interventions

DRUGspinal anesthesia

spinal anesthesia for planned cesarean sections

Sponsors

Hopital Saint Roch
CollaboratorOTHER
University Hospital, Montpellier
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Normal pregnancy * Scheduled caesarean section * Non-multiple pregnancy * Age of patient: 18 years and over * Height of patient: between 155 and 175 cm * Affiliated patients or beneficiaries of a Social Security System * Signature of the patient's consent

Exclusion criteria

* Patient \<18 years * Pathological pregnancy * Multiple pregnancy * Emergency caesarean * Patients who cannot give informed consent (not French speaking) * Refusal of the patient * Contraindications to spinal anesthesia * Contraindications to Prilocaine * Contraindications to Bupivacaine

Design outcomes

Primary

MeasureTime frameDescription
duration of motor blockup to 6 hoursTo compare the duration of motor block after spinal anesthesia with hyperbaric Prilocaïne versus hyperbaric Bupivacaine This evaluation is done every 15 min from the entrance to the recovery room (PACU); the motor block stops being evaluated when the modified bromination score reaches 4

Secondary

MeasureTime frameDescription
Hypotensive episodes1 dayHypotensive episodes
The time between injection and incision1 dayThe time between injection and incision
The duration of the intervention1 dayThe duration of the intervention
The time to return to the standard maternity ward1 dayThe time to return to the standard maternity ward
APGAR score of newborns at birth1 dayAPGAR score of newborns at birth. L'APGAR Apgar score is a method to quickly summarize the health of newborn children. The Apgar scale is determined by evaluating the newborn baby on five simple criteria on a scale from zero to two, then summing up the five values thus obtained. The resulting Apgar score ranges from zero to 10. The five criteria are summarized using words chosen to form a backronym (Appearance, Pulse, Grimace, Activity, Respiration). The test is generally done at one and five minutes after birth, and may be repeated later if the score is and remains low. Scores 7 and above are generally normal, 4 to 6 fairly low, and 3 and below are generally regarded as critically low.
The delay between spinal anesthesia and the first emergency analgesic injection1 dayThe delay between spinal anesthesia and the first emergency analgesic injection
The upper sensory level15 minutes after the LA injectionThe upper sensory level obtained 15 minutes after the LA injection
The delay between spinal anesthesia and the first injection of second-line analgesia1 dayThe delay between spinal anesthesia and the first injection of second-line analgesia : delay between spinal anesthesia ans the need of rescue analgesia
The presence of neuro-sensory disorders within 24 hours postoperatively1 dayThe presence of neuro-sensory disorders within 24 hours postoperatively
The presence of post lumbar puncture syndrome1 dayThe presence of post lumbar puncture syndrome
score de satisfaction1 dayPatient satisfaction score at 24 hours will be assessed by VAS (Visual Analogue Scale); Patients rate satisfaction on VAS from 0-10, 0 being no satisfaction and 10 being total satisfaction
Statifaction of the Surgeon1 dayThe surgeon assessed his satisfaction while the cesarien section. The surgeon satisfaction score at 24 hours will be assessed by VAS (Visual Analogue Scale); Surgeon rate satisfaction on VAS from 0-10, 0 being no satisfaction and 10 being total satisfaction.
Assessment of pain (VAS)1 dayPain on arrival and departure of PACU and at 24 hours. Pain will be assessedby VAS (Visual Analogue Scale); Patients rate pain on VAS from 0-10, 0 being no pain and 10 being the worst pain imaginable..

Countries

France

Contacts

Primary Contactchristophe DADURE, MD, PhD
c-dadure@chu-montpellier.fr467338256

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026