The effectiveness of gabapentin compared to acetaminophen for pain control in postpartum patients following vaginal delivery in Phramongkutklao hospital

Phase 4

Completed

• Conditions: Vaginal delivery; vaginal delivery patients; Postpartum depression; Acetaminophen; Pain in post- Gabapentin; pain control; Postpartum

• Registration Number: TCTR20200323001
• Lead Sponsor: one

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2020-03-15
• Study Start: 2020-03-23
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 220

Inclusion Criteria

Patients who underwent normal vaginal delivery in Phramongkutklao hospital.
Patents who were more than 18 years old.

Exclusion Criteria

Patients who has allergy to acetaminohen or gabapentin.
Patients who received epidural anesthesia.
Patients who had intravenous sedation 2 hours prior to delivery.
Patients with preexisting depression, epilepsy.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postpartum pain after vaginal delivery 30 minutes, 2 hours, 6 hours,12 hours after intervention Visual analogue scale

Secondary Outcome Measures

Name	Time	Method
Side effects of gabapentin and acetaminophen 12 hours after intervention Description