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evaluation of the effect of Novafen and Gelofen in post canal treatment pain decrement

Prophylactic effect of Novafen and Gelofen on post endodontic treatments pain decrement

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014041316973N2
Enrollment
60
Registered
2014-10-04
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

Pharmacokinetics. Other and unspecified diseases of pulp and periapical tissues

Interventions

Intervention 1: In control group : Prescribed 2 capsules orally 1 hour before treatment as placebo. Intervention 2: Novafen group: Prescribed 2 200 mg capsules orally 1 hour befor treatment. Intervent
Treatment - Drugs
In control group : Prescribed 2 capsules orally 1 hour before treatment as placebo
Novafen group: Prescribed 2 200 mg capsules orally 1 hour befor treatment
Gelofen group: Prescribed 2 200 mg capsules orally 1 hour befor treatment

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1.The patient should be able to read , understand and complete the consent form; 2.Patient's consent form has been completed; 3.Teeth with a live pulp that do not have a peri-apical lesion should have been evaluated. Exclusion criteria : 1.Pregnancy; 2.Hypersensitivity to NSAIDs and Sulfonamides; 3.History of asthma associated with nasal polyps; 4.History of chronic use of analgesics or sedatives; 5.Alcohol abuse; 6.Patients with uncontrolled hypertension; 7.Diabetes mellitus; 8.Renal disease, CNS disease, heart disease and liver dysfunction; 9.Cancer or major anomalies confirmed by clinical examinations or laboratory findings; 10.Aged less than 18 and more than 65; 11.Pregnancy or breastfeeding; 12.Analgesic use less than 12 hours to the beginning of the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: One hour before treatment. Method of measurement: 4,8,12,24,48.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Mohammad Kashefi Nejad

Babol Univesity Of Medical Sciences

m.kashefi@mubabol.ac.ir+98 11 1229 1408

Outcome results

None listed

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