The Effect of Paracetamol versus Ketorolac on Postoperative Pain of Cesarean Section

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180425039418N3

Enrollment

140

Registered

2018-12-29

Start date

2018-02-20

Completion date

Unknown

Last updated

2019-01-14

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

Conditions

post-Cesarean pain. Encounter for cesarean delivery without indication

Interventions

Intervention 1: Intervention group 1: Group A paracetamol is injected at a time of zero 1000 mg. Each ampoule of 7.6 mg paracetamol (appendix) contains 1000 mg of acetaminophen, which dissolves each a

Eligibility

Sex/Gender

Female

Age

20 Years to 45 Years

Inclusion criteria

Inclusion criteria: All women who are at the term gestational age with the first pregnancy who are candidates for termination of pregnancy by elective cesarean section

Exclusion criteria

Exclusion criteria: The mothers who have the chronic disorders such as Lupus erythematosus

Design outcomes

Primary

Measure	Time frame
Post-cesarean pain. Timepoint: the first time of pain sensation after surgery, 6 hours after the surgery, 12 hours after surgery, 24 hours after surgery. Method of measurement: VAS visual acuity scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Maryam Razavi

Zahedan University of Medical Sciences

Dr.razavi351@gmail.com+98 543329571522

Outcome results

None listed

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