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Efficacy of prophylactic use Teltonal in comparison with Ibuprofen on post-operative endodontic pain

Efficacy of prophylactic use Teltonal in comparison with Ibuprofen on post-operative endodontic pain

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201404012847N3
Enrollment
57
Registered
2014-05-03
Start date
2014-04-05
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- operative endodontic pain.

Interventions

Intervention 1: One capsule containing starch one hour before the treatment. Intervention 2: One capsule containing 400mg Ibuprofen(Aria, Tehran, Iran) one hour before the treatment. Intervention 3:
Placebo
Treatment - Drugs
One capsule containing starch one hour before the treatment
One capsule containing 400mg Ibuprofen(Aria, Tehran, Iran) one hour before the treatment
One capsule containing 480mg Teltonal (Hexal, Holzkirchen, Germany) one hour before the treatment

Sponsors

Rafsanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: single- root anterior teeth; vital; with severe decay; and spontaneous pain at range of 30-100 in VAS; patients with no noticeable medical history; responses to pulpal tests(cold, heat, and pulp tester). Exclusion criteria: Presence of periapical lesion(in radiography); swelling; fistula; contraindication to study drug consumption; and receiving analgesics in the 12 hours before the treatment.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Post- operative pain. Timepoint: 6,12,24,48 and 72 hours after treatment. Method of measurement: Visual analog scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mohammad Mahdi Yaghooti Khorasani

Dental School, Rafsanjan University of Medical Sciences

m.yaghooti@yahoo.com+98 39 1822 0031

Outcome results

None listed

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