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Comparison of effect of Novafen, Iboprofen and Acetaminophen on pain relief after implant surgeries in posterior region of the upper jaw

Comparison of effect of Novafen, Iboprofen and Acetaminophen on pain relief after implant surgeries in posterior region of maxilla

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016071614440N2
Enrollment
36
Registered
2016-08-10
Start date
2016-07-17
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

implant surgery. ?

Interventions

Intervention 1: Intervention group 1:Ibuprofen 400 milligram tablet, immediately after the surgery and every 8 hours for 2 days. Intervention 2: Intervention group2: Novafen capsule (containing acetam
Treatment - Drugs
Intervention group 1:Ibuprofen 400 milligram tablet, immediately after the surgery and every 8 hours for 2 days
Intervention group2: Novafen capsule (containing acetaminophen 325 mg, ibuprofen 200 mg and caffeine 40 mg) immediately after the surgery and every 8 hours for 2 days
Control group: Acetaminofen 500 miligram tablet, immediately after the surgery and every 8 hours for 2 days

Sponsors

Vice Chancellor for Research of Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria of the study: Informed consent for being included in the study; Candidate patients of implant surgery aged 18?40 years; The hard and soft tissue region should be favorable for implant; Implant replacement without any adjunctive surgery Exclusion criteria of the study: Suffering from a systemic disease; Addictions to alcohol or smoking or every psychotropic substance; Diagnosed sensitivity to NSAIDs, Caffeine or Acetaminophen; Consuming drugs interfering with Ibuprofen, Novafen or Acetaminophen; Receiving any type of analgesics at least four hours before implant surgery

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain Relief after implant surgery. Timepoint: 3h,12h, 24h and 48h after implant surgery. Method of measurement: VAS( Visual Analgesic Scale) 3h after implant surgery; VRS( Verbal Rating Scale) 12h,24h and 48h after implant surgery.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Zarandi

Department of Periodontics of Dental Faculty of Tabriz University of Medical Sciences

dr.alizarandi@gmail.com+98 41 1329 4312

Outcome results

None listed

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