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Comparison of the Effects of celecoxib, celecoxib – caffeine and Ibuprofen on pain control after Surgery

Comparison of the Effects of celecoxib, celecoxib – caffeine and Ibuprofen on pain control after crown lengthening.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201305253813N2
Enrollment
45
Registered
2013-07-24
Start date
2013-09-23
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

Pain after Surgery. Other specified disorders of teeth and supporting structures

Interventions

Intervention 1: Intervention group: Composition celecoxib 150 mg/ caffeine 30 mg, 0.5 hours before surgery and nest doses 1 and 8, 16 and 24 hours after surgery. Intervention 2: Control group: Celecox
Treatment - Drugs
Intervention group: Composition celecoxib 150 mg/ caffeine 30 mg, 0.5 hours before surgery and nest doses 1 and 8, 16 and 24 hours after surgery.
Control group: Celecoxib 150 mg, 0.5 hours before surgery and next doses 1 and 8, 16 and 24 hours after surgery.
Control group: Ibuprofen 400 mg, 0.5 hours before surgery and next doses 1 and 8, 16 and 24 hours after surgery.

Sponsors

Vice chancellor for research and technology, Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: (Inclusion criteria:The patient has no history of systemic disease;The patient has no history of sensitivity to nonsteroidal anti-inflammatory drugs;Age of the patients ranged in age from 20 to 60 years;At least 48 hours prior eaten to study drug is not received analgesic drug;The patient was able to read, understand and complete the questionnaire;Excluded Criteria:Pregnant or lactating patients;Patients with gastrointestinal diseases such as peptic ulcer;Patients with any periodontal surgery within the last 6 months;Patients with severe anxiety and fear when visiting the dentist.)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain after Surgery. Timepoint: Hour 1, 2, 4, 8, 16, 24 and 48 after surgery. Method of measurement: VAS.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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