NCT04747171
Unknown
Not Applicable
A Comparative Study of Postoperative Analgesia of Different Intrathecal Additives for Spinal Anaesthesia in Elective Caesarean Sections
ConditionsPain, Postoperative
Overview
- Phase
- Not Applicable
- Intervention
- intrathecal Magnesium
- Conditions
- Pain, Postoperative
- Sponsor
- Benha University
- Enrollment
- 105
- Primary Endpoint
- analgesic effect
- Last Updated
- 5 years ago
Overview
Brief Summary
we designed this randomized, single -blind, prospective clinical study to test postoperative analgesia of three intrathecal additives in elective caesarean sections which are magnesium, dexamethasone and dexmedetomidine.
Investigators
Baher Said Elshahat Mohamed Abdelhady
Principal Investigator
Benha University
Eligibility Criteria
Inclusion Criteria
- •American Society of Anesthesiologists classII-III adult female patient (age :18 -40 years old )
- •Elective cesarean section under spinal anaesthesia
- •Gestational age \> 37 weeks
- •BMI less than 30 kg/m2
Exclusion Criteria
- •Patient refusal
- •unable to give consent
- •age \< 18 or \> 40
- •BMI more than 30 kg/m2
- •known allergy to the study medication
- •coagulopathies or on anticoagulant medications
- •diabetic neuropathy
- •patients with psychiatric disorders
Arms & Interventions
magnesium intrathecal
Intervention: intrathecal Magnesium
dexamethasone intrathecal
Intervention: intrathecal dexamthasone
dexmedetomidine intrathecal
Intervention: intrathecal dexmedetomidine
Outcomes
Primary Outcomes
analgesic effect
Time Frame: Up to 24 hours after surgery
duration of sensory block
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