A Randomized Comparison Between Erector Spinae Plane Block and Intrathecal Morphine for Analgesia after Cesarean Delivery
- Conditions
- Postoperative pain control after cesarean sections
- Registration Number
- TCTR20200228003
- Lead Sponsor
- Thammasat University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending (Not yet recruiting)
- Sex
- Female
- Target Recruitment
- 140
â–ªOnly women able to provide informed consent will be recruited for study participation
â–ªPatients between 18 and 45 years
â–ªPatients undergoing elective lower segment (transverse incision) cesarean sections under spinal anesthesia
â–ªASA patients greater than or equal to 3.
â–ªAllergies to local anesthetics
â–ªContraindication of neuraxial analgesia.
â–ªPatients with hemodynamic instability
â–ªPatients with systemic diseases: Coagulopathies, chronic use of analgesics, hypertensive disorders.
â–ªPatients with chronic pain
â–ªPatients with inability to comprehend or use the Numeric Rating Scale pain scoring system and difficulty to evaluate pain
â–ªPatients unable to communicate in English or French (in Thai for Thammasat University center)
â–ªIllness associated with pregnancy or high obstetric risk (gestational diabetes, pre-eclampsia, oligo and polyhydramnios, multiple pregnancy, anatomic malformations, etc.)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Dynamic pain 3 6 12 18 and 24 hours after the end of the cesarean delivery Visual Analog Scale
- Secondary Outcome Measures
Name Time Method Pain at rest 3 6 12 18 and 24 hours after the end of the cesarean delivery Visual Analog Scale,Quality of recovery after cesarean delivery 24 hours after the end of the cesarean delivery ObsQoR11 Questionaire,Chronic pain 3 months after the cesarean a modification of the brief pain inventory