The effect of acetaminophen drip on pain after cesarean section

Comparison of intravenous acetaminophen effect with 24-hour and routine drip on control of pain in patients undergoing cesarean section

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180708040381N3

Enrollment

Registered

2022-02-17

Start date

2017-10-23

Completion date

Unknown

Last updated

2022-03-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

post operative pain.

Interventions

Intervention 1: After the patient was fully conscious and in recovery in the 24-hour drip group, 2 mg / kg morphine and 4000 mg of acetaminophen were poured into the PCA pump and injected into the pat

Eligibility

Sex/Gender

Female

Age

16 Years to 40 Years

Inclusion criteria

Inclusion criteria: Women aged 16 to 40 years Candidate for cesarean section No smoke and opioids consumption ASA class 1 or 2

Exclusion criteria

Exclusion criteria: Allergy to any of the drugs used in study Liver disease History of seizure

Design outcomes

Primary

Measure	Time frame
Pain Score. Timepoint: First 24 hr After Surgery Every 6 hr. Method of measurement: VAS Score.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mehdi Izadi Zaman Abadi

Esfahan University of Medical Sciences

mimi_izadi2@yahoo.com0098312724538

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026