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Effectiveness of Alveogyl and Cutanplast Dressing on Postoperative Pain Following Tooth Extraction: A Clinical Trial

Effectiveness of Alveogyl and Cutanplast Dressing on Postoperative Pain Following Tooth Extraction: A Clinical Trial

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04779476
Enrollment
50
Registered
2021-03-03
Start date
2021-03-04
Completion date
2021-12-31
Last updated
2021-10-12

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

Conditions

Facial Pain, Pain, Orofacial, Pain, Postoperative

Keywords

Alveogyl, Eugenol, Dental extraction, Post extraction pain

Brief summary

This study aims to assess the post-dental extraction pain following the application of two different dressing materials. Alvogyl® and Absorbable gelatin sponges

Detailed description

Effective postoperative pain relief improves the quality of recovery and the resumption of normal activities. Many options are available for postoperative pain relief following tooth extraction including systemic analgesic, intra-alveolar socket dressing medicaments, and follow the postoperative instructions; the choice of the medication determined by drug availability, chance of side effect of some drugs and financial considerations. The use of intra-alveolar dressing materials is widely suggested in the literature such as Alvogyl® that used as palliative treatment which includes eugenol (analgesic, anti-inflammatory), iodoform (antimicrobial), and butamen (anesthetic). Absorbable gelatin sponges contain haemostatic material and may be used for local application in surgical procedures where traditional haemostasis is difficult. In addition to its haemostatic effect, an absorbable gelatin sponge can be used as a drug reservoir to provide sustained release of drugs The aim of this study is to measure the pain intensity after using socket dressing materials following tooth extraction.

Interventions

OTHERSocket Dressing

Following dental extraction immediately, the socket will be dressed with one of the materials tested

Sponsors

Riyadh Elm University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
13 Years to 22 Years

Inclusion criteria

* Single tooth extraction * Upper and lower teeth

Exclusion criteria

* Surgical extraction * Medically compromised patients * Presence of active infection * Presence of pathology

Design outcomes

Primary

MeasureTime frameDescription
3 hrs post extraction painthree hours after the extractionVisual analogue scale score for pain
6 hrs post extraction painsix hours after the extractionVisual analogue scale score for pain
12 hrs post extraction paintwelve hours after the extractionVisual analogue scale score for pain
24 hrs post extraction paintwenty-four hours after the extractionVisual analogue scale score for pain

Countries

Saudi Arabia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026