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Analgesic effect of paracetamol and meperidine after cesarean section.

Clinical trial of comparison between the effect of paracetamol (Apotel) and meperidine ( pethidine) on the pain in the first 24 hours after cesarean section.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201405262624N17
Enrollment
100
Registered
2015-04-25
Start date
2014-08-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Cesarean delivery. Single delivery by caesarean section

Interventions

Intervention 1: Intervention group: After finishing cesarean section and in the recovery room , pain of the patient has been determined using VAS . Then diclofenac suppository 100 milligram plus para
Treatment - Drugs
Intervention group: After finishing cesarean section and in the recovery room , pain of the patient has been determined using VAS . Then diclofenac suppository 100 milligram plus paracetamol ( Apotel
Control ( mepiridine) group: After finishing cesarean section and in the recovery room , pain of the patient has been determined using VAS . Then diclofenac suppository 100 milligram plus mepiridine (

Sponsors

Vice chancellor for research ,Iran University of Medical Sciences.
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: all patients after cesarean section with normal body mass index( between 18.5 and 25). Exclusion criteria: Drug abuse; history of allergy to paracetamol or mepiridine; history of hepatitis; renal failure; heart failure; respiratory disease;CNS disorders; coagulopathy; sedative use; psychiatric disorders and complication of cesarean section.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain . Timepoint: 0-1-2-4 and 6 hours after drug administration. Method of measurement: VAS.

Secondary

MeasureTime frame
Need to more analgesic. Timepoint: 0-1-2-4 and 6 hours after drug administration. Method of measurement: questionair.;Paracetamol adverse effects. Timepoint: 0-1-2-4 and 6 hours after drug administration. Method of measurement: VAS.;Side effects of meperidine. Timepoint: 0-1-2-4 and 6 hours after drug administration. Method of measurement: VAS.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Kashanian

Iran University of Medical Sciences

maryamkashanian@yahoo.com+98 21 5563 3244

Outcome results

None listed

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