Oral Versus Intravenous Acetaminophen for Postoperative Pain Control

• Status: Suspended
• Trial end date: 2022-12-31
• Target enrollment: 0
• Participant gender: Female

Summary

The investigators are going to study the difference in postoperative pain control after administration of oral versus intravenous formulation of acetaminophen

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

Details

• Lead Sponsor: Northwell Health
• Treatments: Acetaminophen

Criteria

Inclusion Criteria:

1. Provision of signed and dated informed consent form

2. Stated willingness to comply with all study procedures and availability for the duration of the study

3. Female, aged 18-45

4. Ability to take oral medication and be willing to adhere to the study intervention regimen

Exclusion Criteria:

1. Known clinically significant liver disfunction

2. Known allergic reactions to components of acetaminophen such as angioedema, anaphylaxis or other

3. Known current substance use disorder

4. Chronic pain syndrome

5. Weight less than 50 kg