Sacral Erector Spinae Plane Block in Normal Birth

ConditionAnalgesia
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-42
SponsorKonya City Hospital

About this trial

Pregnant women feel severe pain during normal birth and in the postpartum period. Preventing pain during and after birth is very important for both the mother and the baby. Rapid recovery in the postoperative period in pregnant women is very important for both mother and baby. To evaluate this recovery, the quality of recovery-10 scores developed by Shalev et al. are used in pregnant women. Our study will be the first in the literature to use sacral erectör spinae plane block (S-ESPB) in normal birth. Our primary aim in this study is to evaluate the effects of S-ESPB on the quality of recovery and recovery at the 24th hour in pregnant women who will undergo vaginal birth with epidural analgesia, using the Quality of Recovery-10T scores.

Eligibility criteria

Qualifiers

36-42. Pregnant women who are their gestational age and request epidural anesthesia

Pregnant women aged 18-42 with ASA II

Pregnant women who will stay in the hospital for at least 24 hours

Primiparous pregnant women who will have a planned normal birth

Disqualifiers

Pregnant women who do not want to give consent

Regional anesthesia is contraindicated

Pregnant women who use anticoagulants and have an abnormal bleeding profile

Pregnant women with infection in the area to be treated

Trial design

Treatments tested in this trial

  • % 0.25 bupivakain 20cc
  • 20 cc saline

Treatment groups

40 Participants
are divided into 2 treatment groups

Sponsors and collaborators