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Comparison of the prophylactic analgesic effects of acetaminophen and celecoxib in patients undergoing rhinoplasty operation

Comparison of the prophylactic analgesic effects of acetaminophen and celecoxib in patients undergoing rhinoplasty operation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012102111191N1
Enrollment
70
Registered
2013-01-19
Start date
2012-03-20
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

post surgical pain. Follow-up care involving plastic surgery of head and neck

Interventions

Intervention 1: Intervention: Tab Celecoxib 200 mg, 30min before operation, every 12 hour in first 24 hours. Intervention 2: Control group: Tab Acetaminophen 500 mg, 30 min before operation, every 6 h
Treatment - Drugs
Intervention: Tab Celecoxib 200 mg, 30min before operation, every 12 hour in first 24 hours
Control group: Tab Acetaminophen 500 mg, 30 min before operation, every 6 hour in first 24 hours

Sponsors

Vice Chancellor for Research of Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: functional class I; completed informed consent form Exclusion criteria: history of allergy to acetaminophen or sulfonamides; unwillingness to participate in the study; complications of rhinoplastic surgery; severe drugs side effects; current sever illnesses such as: cardiovascular disease, diabetes mellitus type1, obstructive pulmonary disease and asthma, sever HTN, epilepsy, renal or liver dysfunction, analgesic consumption 12 hours before the surgery, alcohol or drug addiction.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain severity. Timepoint: before operation, 2hours after rhinoplasty, every 6 hour till 24 hours. Method of measurement: Visual Analogue Scale(VAS).;Requested analgesic dose. Timepoint: first 24 hours. Method of measurement: mg.

Secondary

MeasureTime frame
Surgical site bleeding. Timepoint: first 24 hours. Method of measurement: Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAtena Esmaeli

Pharmacy School of Shahid Beheshti University of Medical Sciences

a.esmaeli@arakmu.ac.ir+98 21 8866 2340

Outcome results

None listed

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