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
This trial does not accept healthy volunteersQualifiers
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
Design model
Crossover
Treatments tested in this trial
% 0.25 bupivakain 20cc
Other interventionPregnant women in group S will be given 0.25% bupivacaine, 10 cc on each side.
20 cc saline
Other interventionPregnant women in Group K will be given 10 cc of saline on both sides.
Treatment groups
40 Participants
are divided into 2 treatment groupsGroup A: SACRAL EREKTÖR SPİNAE PLANE BLOKActive comparator 1 intervention
Group B: control groupActive comparator 1 intervention
Trial outcomes
Primary outcomes
1
Quality of recovery (10T) scores
The primary evaluation criterion will be the recording of Quality of Recovery-10T scores, which indicate the quality of recovery of pregnant women at the 24th hour after birth. Quality of Recovery-10T ( Minumum: 0 = Very bad, Maximum: 100= Perfect).
Time frame
One daySponsors and contacts
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Source ClinicalTrials.gov