Efficacy of paracetamol for pain reduction

Efficacy of prophylactic paracetamol injection for pain reduction after cesarean

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20181001041196N1

Enrollment

Registered

2019-03-25

Start date

2018-11-22

Completion date

Unknown

Last updated

2019-04-23

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

Conditions

Pain localized to other parts of lower abdomen. Pain localized to other parts of lower abdomen

Interventions

Intervention 1: Intervention group: this group includes thirty 38 weeks pregnant women. 1 gr (100 cc) intravenous prophylactic paracetamol (manufactured by Abidi) at one time, 30 minutes before spin

Eligibility

Sex/Gender

Female

Age

20 Years to 35 Years

Inclusion criteria

Inclusion criteria: Elective cesarean Spinal anesthesia Single tone pregnancy More than 38weeks pregnancy

Exclusion criteria

Exclusion criteria: Addiction to drug Cardiac ,hepatic,pulmonary diseases Allergy to paracetamol

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: 1 hour after ceassarean,12hour after cesarean ,18hour after cesarean and 24hour after cesarean. Method of measurement: Vas score.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSahar yahyapour

Shahid Beheshti University of Medical Sciences

Sahar_yahyapour@yahoo.com+98 21 2243 2525

Outcome results

None listed

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