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Comparison of The prophylactic effect of Zintoma and Ibuprofen in Post-Endodontic pain

Comparison of The prophylactic effect of Zintoma and Ibuprofen in Post-Endodontic pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138903174116N1
Enrollment
90
Registered
2010-10-10
Start date
2010-03-20
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

Diseases of pulp and periapical tissues.

Interventions

Intervention 1: Placebo group: 1.5 hour before treatment, 2 placebo capsules are used and 1 hour later, ie 0.5 hour before treatment another 2 placebo capsules are used. Intervention 2: Ibuprofen grou
Placebo
Treatment - Drugs
Placebo group: 1.5 hour before treatment, 2 placebo capsules are used and 1 hour later, ie 0.5 hour before treatment another 2 placebo capsules are used
Ibuprofen group: 0.5 hour before treatment, 1 capsule containing 400 mg ibuprofen is used
Zintoma group: 1.5 hour before treatment two 500 mg zintoma capsules are used and 1 hour later, ie 0.5 hour before treatment another two 500 mg zintoma are used

Sponsors

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

Eligibility

Sex/Gender
All
Age
19 Years to 64 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1: Age between 18 and 65 2: No history of the following diseases: mitral valve prolapse, myocardial rheumatism, artificial valve or joint, myocardial infarction, brain stroke, uncontrolled hypertension, hepatitis, seizure, bleeding disorders, peptic ulcer, liver or kidney diseases 3: No history of allergy to NSAIDs or Zingiber Officinale 4: No pregnancy, no breast feeding 5: No other drug consumption at least four hours before study commense 6: Severity of spontaneous pain must be at least five 7: Patients ability to read, comprehend and complete the questionaire and VAS 8; completion of informed consent

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: before intervention and 4, 8, 12, 24, 48 and 72 hours after intervention. Method of measurement: using VAS registration questionaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohsen Ramazani

Babol Medical University- Faculty of Dentistry

m.ramzani@mubabol.ac.ir+98 11 1222 4032

Outcome results

None listed

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