Skip to content

Effect of CYP2C9*3 Polymorphism on Ibuprofen in Pakistani Population

Effect of CYP2C9*3 rs 1057910 Polymorphism on the Efficacy and Tolerability of Ibuprofen After Molar Tooth Extraction in Pakistani Population

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05983042
Enrollment
200
Registered
2023-08-09
Start date
2022-11-01
Completion date
2023-07-31
Last updated
2026-06-02

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

Conditions

Healthy Volunteers

Brief summary

The goal of the study was to identify the effect of CYP2C9 gene polymorphism in the Pakistani population. The main question it aims to answer were: * to evaluate the effect of this genetic polymorphism on the clinical efficacy of Ibuprofen * to evaluate the effect of this genetic polymorphism on the clinical tolerability of Ibuprofen Participants were prescribed Ibuprofen after molar tooth extraction.

Detailed description

The goal of this study was to identify the effect of CYP2C9\*3 gene polymorphism in the Pakistani population, due to the high prevalence of this variant in the Pakistani Population The main question it aims to answer were: * to evaluate the effect of this genetic polymorphism on the clinical efficacy of Ibuprofen * to evaluate the effect of this genetic polymorphism on the clinical tolerability of Ibuprofen Participants were prescribed Ibuprofen after molar tooth extraction. The blood samples of the participants were taken and further genotyping was performed using conventional tetraARMS PCR. The results were visualized by gel electrophoresis.

Interventions

DRUGIbuprofen 400 mg

Ibuprofen 400 mg TDS

DRUGPlacebo

Placebo tablet

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Pakistani individuals * Absence of systemic diseases * Extractions required based on orthodontic, periodontal, and endodontic indications

Exclusion criteria

* history of bleeding or gastrointestinal ulcers * allergic to ibuprofen or other NSAIDs. * Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Visual Analogue Scalethree daysA Visual Analogue Scale (VAS) is one of the self-administered pain rating scales, to measure pain intensity. The pain was interpreted as no pain (0-4 mm), mild pain(5-44 mm), moderate pain (45-74 mm), and severe pain (75-100 mm).

Secondary

MeasureTime frameDescription
General Assessment of Side Effects scalethree daysThe self-rating scale General Assessment of Side Effects (GASE), is about the most frequent side effects in clinical trials of different drugs. Every symptom (dyspepsia, nausea, diarrhea) had to be answered twice: first, participants had to rate the intensity of this symptom during the last 3 days, and second, if this symptom was present, participants had to rate whether they attribute it to current drug intake.

Countries

Pakistan

Contacts

PRINCIPAL_INVESTIGATORAmmarah Amjad, BDS

Riphah International University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 3, 2026