Actively Recruiting
Sacral Erector Spinae Plane Block in Normal Birth
Led by Konya City Hospital · Updated on 2024-10-08
40
Participants Needed
1
Research Sites
94 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Sacral Erector Spinae Plane Block in Normal Birth
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pregnant women aged 18 to 42 years with ASA II
- Gestational age between 36 and 42 weeks requesting epidural anesthesia
- Planned normal vaginal birth for first-time mothers
- Singleton pregnancy with head-down baby position
- Willing to stay in the hospital for at least 24 hours
You will not qualify if you...
- Pregnant women who do not consent to participate
- Contraindications to regional anesthesia
- Use of anticoagulants or abnormal bleeding profile
- Infection at the treatment site
- Emergency births or births using instruments like forceps or vacuum
AI-Screening
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Trial Site Locations
Total: 1 location
1
Konya City Hospital
Konya, Turkey (Türkiye), 42020
Actively Recruiting
Research Team
M
MUHAMMED H SATICI, M.D
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
OTHER
Number of Arms
2
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