Abdominoplasty Under Spinal Anesthesia

Ain Shams University

Status: Completed

Conditions: Spinal Anesthesia Suitability for Abdominoplasty

Treatments: Drug: Propofol 10 Mg/mL Intravenous Emulsion

Study type: Interventional

Funder types: Other

Identifiers

NCT03810547

ASUH1011/17

Details and patient eligibility

About

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

Full description

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.

Enrollment: 200 patients

Sex: All

Ages: 18 to 55 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• All patients between 18-55 years
• ASA I and II

Exclusion criteria

• BMI more than 35 years
• Contraindications for regional anesthesia

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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200 participants in 2 patient groups

Spinal anesthesia

Active Comparator group

Description:

Patients undergoing abdominoplasty under spinal anesthesia may need to drug administration like propofol or ketamine or change anesthesia to general anesthesia.

Treatment:

Drug: Propofol 10 Mg/mL Intravenous Emulsion

General anesthesia

No Intervention group

Description:

General anesthesia for abdominoplasty