CompletedNot Applicable

Propacetamol to Reduce Post Cesarean Section Uterine Contraction Pain

Taiwan100 participantsStarted 2019-08-12

Plain-language summary

To evaluate that perioperative regular usage of propacetamol to reduce post cesarean section uterine contraction pain and opioid consumption

Who can participate

Age range20 Years – 60 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Pregnancy more than 36 weeks which is expected to receive Caesarean section * Post Caesarean section woman, age greater than or equal to 20 years old * ASA physical status class 1 or 2 Exclusion Criteria: * ASA physical status class 3 or above * Less than 20 years old * Past caesarean section for longitudinal wounds * Undergone major abdominal surgery * Chronic pain * Allergic to morphine or Propacetamol * Liver dysfunction * Treatment with anticoagulant * Emergency operation

What they're measuring

Change of pain assessed by NRS

Timeframe: Every 8 hours from post-anesthesia care unit to 2 days after the cesarean section

Incidence of treatment-relate adverse events

Timeframe: Two days after the cesarean section

Opioid consumption

Timeframe: Two days after the cesarean section

Trial details

NCT IDNCT03878082

SponsorMackay Memorial Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-12-30

View on ClinicalTrials.gov More Uterine Pain trials