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Comparison of the analgesic effect of three analgesics before surgery in pain after mandibular wisdom tooth surgery

Comparing the analgesic effect of single-dose preoperative administration of noblegin, celecoxib and advalgin ER on demand for next dose of analgesic in mandibular third molar surgery

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20221207056746N1
Enrollment
120
Registered
2023-05-31
Start date
2022-11-02
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

postoperative pain. Pain, not elsewhere classified

Interventions

Intervention 1: Intervention group 1: pre-operative consumption of one Nobelgin tablet manufactured by Pars Daru Pharmaceuticals, each tablet contains acetaminophen 300 mg, caffeine 15 mg and codeine

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 29 Years

Inclusion criteria

Inclusion criteria: Healthy patients (ASA class I) Candidates of prophylactic removal of mandibular third molar,full or partial bony impaction confirmed by panoramic X-ray Requiring soft tissue flap, bone manipulation and bone removal No medication consumption in the past 21 days The presence of the first and second molars Good oral hygiene Absence of pericoronitis or inflammation signs Absence of local or systemic infection

Exclusion criteria

Exclusion criteria: Smokers Pregnant or breastfeeding women or women of child bearing potential not using adequate contraception Allergy or hypersensitivity to study treatments, rescue medication (rm) or any other nsaids, opioids and acetyl salicylic acid History of NSAID-sensitive asthma History of or the suspicion of drug or alcohol abuse Apical radiolucent image in target tooth Consmuption of central nervous system depressants Pre-existing pain and acute inflammation Inability to understand or perform the study procedure Psychosis Consumption of caffeine-containing beverages, chocolate, or alcohol within 4 hours prior to surgery Oral contraception use Being in the menstrual period Any contraindication of cox-2 inhibitors use

Design outcomes

Primary

MeasureTime frame
Postoperative pain intensity. Timepoint: 4hours & 7 hours postsurgery,the first day and the third day after surgery. Method of measurement: Visual Analogue Scale.;The time of first analgesic intake. Timepoint: one week after surgery. Method of measurement: Referring to document.;The number of patients who needed analgesics (vas=4). Timepoint: One week after surgery. Method of measurement: Referring to patients' documents.;The total number of analgesics used. Timepoint: One week after surgery. Method of measurement: Referring to patients' documents.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmirhossein Moaddabi

Mazandaran University of Medical Sciences

A.moaddabi2@gmail.com+98 11 3335 6194

Outcome results

None listed

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