Actively Recruiting

Phase Not Applicable
Age: 18Years - 42Years
FEMALE
NCT06221332

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

Age: 18Years - 42Years
FEMALE

Eligibility Criteria

Eligible

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
Not Eligible

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

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Konya City Hospital

Konya, Turkey (Türkiye), 42020

Actively Recruiting

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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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