Analgesic effect of paracetamol in pain managment after cesarean section

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20150519022320N17

Enrollment

240

Registered

2019-01-18

Start date

2017-09-23

Completion date

Unknown

Last updated

2019-01-29

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

Conditions

After cesarean pain.

Interventions

Intervention 1: Intervention group: A group of pregnant women who will receive one gram of intravenous Paracetamol half an hour before the onset of cesarean section. Intervention 2: Control group: A g

Eligibility

Sex/Gender

Female

Age

18 Years to 40 Years

Inclusion criteria

Inclusion criteria: term pregnancy elective cesarean section

Exclusion criteria

Exclusion criteria: History of cardiovascular disease Hypertension Diabetes Hepatic failure Renal failure Drug abuse Taking psychiatric medications Pain before cesarean

Design outcomes

Primary

Measure	Time frame
Pain score in visual analog scale. Timepoint: measurement of pain by VAS in 0, 1,2,4,6,12 and 24 hour after cesarean section. Method of measurement: pain measured by VAS.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSakineh Mirzaei Khalilabadi

Rafsanjan University of Medical Sciences

mirzaie_sk@yahoo.com+98 34 3428 9118

Outcome results

None listed

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