Bolus Administration of Intravenous Lidocaine at the Time of Abdominal Hysterectomy

• Status: Completed
• Trial end date: 2020-08-01
• Target enrollment: 0
• Participant gender: Female

Summary

The objective of the study to evaluate whether a bolus administration of intravenous lidocaine decreases postoperative pain and represents an opioid-minimizing strategy after abdominal hysterectomy compared with placebo.

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Aswan University Hospital
• Treatments: Anesthetics; Lidocaine

Criteria

Inclusion Criteria:

• Women ranging age between 35-60 years a who undergoing elective total abdominal hysterectomy

Exclusion Criteria:

• Participants had known sensitivity to lidocaine

• Participants had difficulty in intubation

• Participants were on chronic pain medication or already on long-term opioids

• Participants smokers

• Participants with disabilities who were unable to communicate pain levels

• refuse to consent