The effectiveness of acetaminophen/tramadol rectal suppository for the relieve of perineal pain after normal vaginal delivery: randomized controlled trial.
Phase 2
Recruiting
- Conditions
- pain score after normal vaginal deliveryside effects of acetaminophen/tramadol rectal suppositoryacetaminophen/tramadolrectal suppositoryvaginal deliverypain
- Registration Number
- TCTR20170105003
- Lead Sponsor
- Thammasat University Research Funding
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 200
Inclusion Criteria
term paturients undergoing normal vaginal delivery with episiotomy wound grade 2 or more
Exclusion Criteria
history of acetaminophen/tramadol allergy
operative vaginal delivery
abnormal fetal presentation
indicated for cesarean section delivery
multigestation
reject to participate
complication of episiotomy
painless labor
known major underlying disease
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain score 0, 6, 12, 24 hours Visual analog scale
- Secondary Outcome Measures
Name Time Method Side effects of acetaminophen/tramadol rectal suppository in 24 hours Questionaire