Large Volume Bupivacaine 0.5% Versus Small Volume in Elective Caesarean Section

Cairo University30 enrolled

Overview

To test the safety of high dose spinal in elective CS after prolonged sitting position.

This is a prospective double-blind randomized study, designed to include cases in two groups (using epical program for sample size calculation), one study groups and one control group (parallel). Each group should have at least 30 female patients scheduled for elective caesarean section with a total of 60 cases.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

Conditions

Spinal Anesthesia

Interventions

intrathecal 15 mg bupivacaineDRUG

spinal anesthesia with a large dose of bupivacaine 0.5% in elective caesarean section

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 45 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Full term pregnant female indicated for the elective section under spinal anesthesia with no history of medical importance Exclusion Criteria: * Urgent cases, emergency cases, adverse medical history, anticoagulant treatment, associated pregnancy complication, failed spinal, surgical complication or refusal

Locations (1)

Cairo University

Cairo, Giza Governorate, Egypt

RECRUITING

Outcomes

Primary Outcomes

vital signs

blood pressure, heart rate

Time frame: 45 minutes

Secondary Outcomes

complications

nausea, vomiting and total spinal

Time frame: 45 minutes

Central Contacts

Hassan Ali, lecturer

CONTACT

1001733687 hassan364@hotmail.com

Data from ClinicalTrials.gov

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