The effect of analgesics on post operative pain following root canal treatment of primary teeth

The effect of Iboprofen premedication on postoprative pain following primary teeth pulpotomy with calcium enriched material:a randomized clinical trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2016102930553N1

Enrollment

Registered

2017-01-20

Start date

2016-11-21

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

Reversible pulpitis. Pulpal and periodontal tissue diseases

Interventions

Intervention 1: Intervention: Ibuprofen, 45 min before treatment, 0.8 mg/kg. Intervention 2: Control: placebo, 45 min before treatment.

Treatment - Drugs

Intervention: Ibuprofen, 45 min before treatment, 0.8 mg/kg

Control: placebo, 45 min before treatment

Eligibility

Sex/Gender

All

Age

6 Years to 10 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria: patients aged 6-10 years old who had bilateral primary molar teeth with carious lesion; teeth were suitable for restoration; no tenderness to percussion; no pain except after eating; no clinical and/or radiographic signs of pulp degeneration; less than two-thirds of the root length affected with physiological resorption; no systemic diseases that contra-indicatedconservative pulp therapy (such as leukemia and some types of malignancies)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: immediately, 1 day, 2 days and 3 days after intervention. Method of measurement: VAS scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Sara Esmaili

Dental Faculty of Kerman University of Medical Sciences

saraesmaili65@yahoo.com+98 34 3211 9028

Outcome results

None listed

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