Overview
Dexmedetomidine for Intermittent Epidural Boluses Versus Continuous Epidural Infusion for Labour Epidural Analgesia
Status:
Not yet recruiting
Not yet recruiting
Trial end date:
2025-10-01
2025-10-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
The aim of this study is to compare two modes of labour epidural analgesia: programmed intermittent epidural boluses (PIEB) versus continuous epidural infusion (CEI), with patient controlled epidural analgesia (PCEA), using dexmedetomidine in addition to low-dose bupivacaine and through measuring the total volume of local anesthetic received through patient controlled epidural analgesia per hourPhase:
Phase 2/Phase 3Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Assiut UniversityTreatments:
Bupivacaine
Dexmedetomidine
Criteria
Inclusion Criteria:- Age 18 - 45 years
- Scheduled for normal vaginal delivery
- ASA physical status ӀI-IӀӀ.
- Singleton non-complicated pregnancy.
- At least 36 weak of gestation.
- Vertex presentation.
Exclusion Criteria:
- Patient refusal to epidural analgesia.
- History of cardiac, liver, or kidney diseases.
- History of allergy to amide local anesthetics or study medications.
- Any neurological problem.
- History of chronic opioid analgesic use.
- Any contraindication of regional anesthesia.
- Evidence of intrauterine growth restriction or fetal compromise.
- Failed or unsatisfactory analgesic block.
- Body mass index ≥40 kg/m2