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Comparison of the Administration of Nobelgin and Novafen in Pain Control After Implant

Comparison of the Administration of Nobelgin and Novafen in Pain Control After Dental Implants Surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240927063186N1
Enrollment
50
Registered
2024-10-23
Start date
2024-08-22
Completion date
Unknown
Last updated
2025-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental implant surgery.

Interventions

Intervention 1: Intervention group: receiving Novafen, (CombinationTablet Includes: 325 mg Acetaminophen, 200 mg Ibuprofen and 40 mg Caffeine) (Iran Daroo, Tehran, Iran), one capsule every 6 hours for

Sponsors

Oroumia University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age range above 18 years to 40 years Sufficient alveolar bone thickness of at least 6.5 mm in the area to be implanted Clients with ASA 1 or 2 No need for bone graft(GBR)

Exclusion criteria

Exclusion criteria: History of allergy to NSAIDs Referral of the patient to the office with active bleeding Tooth decay in the vicinity of the surgery site History of housing consumption in the last 24 hours Mental disorders and severe pain reactions Elderly and people with osteodegenerative diseases such as uncontrolled diabetes and rheumatoid arthritis People who consume bisphosphonates People who drink alcohol

Design outcomes

Primary

MeasureTime frame
Pain intensity using the Verbal Rating Scale (VRS). Timepoint: at 1, 12, 24, 48 and 72 hours after surgery. Method of measurement: Verbal Rating Scale (VRS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Mirzaei

Oroumia University of Medical Sciences

Z.mirzaei.8310@gmail.com+98 44 3224 2564

Outcome results

None listed

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