IRCT20170417033491N2CompletedPhase 3
Comparison of the effect of Bupivacaine 0.5% , Lidocaine 5% , Pethidine , Lidocaine 5% & intratecal on the incidence of decrease blood pressure , nausea and vometing for elective caesarean section
Gerash University of Medical Sciences0 sites75 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 3
- Status
- Completed
- Sponsor
- Enrollment
- 75
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 years to 45 years (—)
- Sex
- Female
Inclusion Criteria
- •Age 45 - 18 years
- •Term pregnancy (42-37 weeks)
- •Willingness to participate in the study
- •NPO (Nil Per Os)
- •Elective caesarean section
Exclusion Criteria
- •Operation duration more than 80 minutes
- •Using ritodrine or other beta tocolytic
- •Fetal abnormalities or pregnancy complications
- •Failure in performing spinal
- •Low level of blocks (block level lower than T8)
- •Stomachache; metabolic diseases; hypertension; nausea and vomiting before surgery
- •Any underlying diseases
- •Complications during surgery
- •Arterial or venous disease in lower extremities
- •Defects in the immune system and gestational diabetes
- •Alcoholism and opium addiction
- •Malnutrition
Investigators
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