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Comparison of pain killer patch and Pain killer tablets in management of pain after bilateral teeth extractions

Comparative Evaluation of Transdermal Diclofenac and Oral Diclofenac in Management of Post Operative Pain in Bilateral Extractions - An Invivo study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/01/011482
Enrollment
17
Registered
2018-01-23
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- post extraction pain management with transdermal diclofenac diethyleamine and oral diclofenac sodium.

Interventions

Intervention1: Diclofenac Diethylamine 100mg: Proprietary name - Nupatch 100, Manufacturer - Zydus Cadila Healthcare Ltd , Formulation - transdermal patch, Dosage - 100mg, Frequency and duration - onc

Sponsors

Swaminathan
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient in the age group of 18-55 years will be selected irrespective of sex, caste, religion and socio-economic status. 2. Bilaterally extraction of same teeth in adjacent quadrants of the jaw. 3. Patients who agreed to follow the study protocol.

Exclusion criteria

Exclusion criteria: 1. Uncontrolled systemic diseases. 2. Patient with anti-coagulant therapy. 3. Patient allergic to diclofenac or any NSAIDS 4. Patient under medication of NSAIDS or corticosteroids for any other illness. 5. Patient with history of peptic ulcer. 6. Tender teeth and third molars and periodontally compromised teeth. 7. Uncooperative patients not willing to commit to an appropriate post procedure follow-up.

Design outcomes

Primary

MeasureTime frame
post operative pain score evaluation in Visual analog scale (0-10) Verbal rating scale (0-3) Pain relief scale (0-3) Pain intensity scale (0-3) Timepoint: post operative pain score is evaluated in post operative 2 hours, 6 hours, 12 hours for three consecutive days.Scoring is stopped when the first emergency medication for pain tablet paracetamol 500mg is consumed by patient.There after number of tablet paracetamol 500mg consumed is calculated.

Secondary

MeasureTime frame
when patient start consuming emergency pain tablets paracetamol500mg, number of tablet paracetamol 500mg consumed is calculated. Timepoint: Number of paracetamol 500mg tablet consumed in a day is noted for three consecutive days.

Countries

India

Contacts

Public ContactDr C Swaminathan

Sree Mookambika Institute of Dental Science

dhineksh@gmail.com

Outcome results

None listed

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