Abdominoplasty Under Spinal Anesthesia

Ain Shams University200 enrolled

Overview

100 patients undergoing abdominoplasty under spinal anesthesia. 100 patients undergoing abdominoplasty under general anesthesia

200 patients, American Society of Anesthesiologists (ASA) physical status classes I and II, were enrolled in this feasible study. All patients were subjected to abdominoplasty operation under spinal anesthesia or general anesthesia. Any intraoperative complications like hypotension, bradycardia, pain, nausea and vomiting related to spinal anesthesia were managed and recorded. Postoperative visual analogue scale (VAS) was used to assess pain severity and the need for analgesia to be administered.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

DOUBLE

Enrollment

200

Conditions

Spinal Anesthesia Suitability for Abdominoplasty

Interventions

Propofol 10 Mg/mL Intravenous EmulsionDRUG

when spinal anesthesia is not satisfactory intervention drugs are used

Eligibility

Sex: ALLMin age: 18 YearsMax age: 55 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * All patients between 18-55 years * ASA I and II Exclusion Criteria: * BMI more than 35 years * Contraindications for regional anesthesia

Locations (1)

Ain Shams University

Cairo, Egypt

Outcomes

Primary Outcomes

Change in Pain sensation: Visual analogue scale

Visual analogue scale for Pain assessment from 1 with least pain to 10 with maximum pain felt

Time frame: pain assessment during the operation and every 4 hours for 12 hours

Patients satisfaction: Satisfaction score changes

Satisfaction score with maximum score is fully satisfied and least is completely disagree

Time frame: Intraoperative assessment every 30 minutes till end of surgery.

Data from ClinicalTrials.gov

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