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A Comparative Analysis of Facial Elastic Bandage in Reducing Swelling and Pain After Medium and High-Difficulty Impacted Mandibular Third Molar Extraction

A Comparative Analysis of Facial Elastic Bandage in Reducing Swelling and Pain After Medium and High-Difficulty Impacted Mandibular Third Molar Extraction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127026
Enrollment
Unknown
Registered
2026-06-23
Start date
2023-09-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

None

Interventions

Control group:Routine post-operative care instructions are provided after tooth extraction, with no additional intervention factors.
Experimental group:In addition to informing the patient of the routine post-operative care measures after tooth extraction, a compression headgear should be worn continuously within 48 hours after the

Sponsors

Affiliated Stomatological Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
17 Years to 40 Years

Inclusion criteria

Inclusion criteria: Patients who visited the Department of Oral and Maxillofacial Surgery of the Yuexiu Branch of Guangzhou Medical University Affiliated Hospital and requested the extraction of impacted wisdom teeth in the mandible were selected; Inclusion criteria: 1. No gender restrictions; 2. Age ranging from 17 to 40 years old; 3. Radiological examination falls within the Pell & Gregory classification of types II to III, middle and low-position mandibular impacted wisdom teeth; 4. Clinical examination indicates that the extraction surgery requires incision and flap opening, bone removal to expose the wisdom teeth.

Exclusion criteria

Exclusion criteria: The following patients should be excluded: 1. Those with hypertension, cardiovascular diseases, or diabetes; 2. Those currently using central nervous system depressants or analgesics; 3. Those with a history of smoking; 4. Those allergic to anesthetics or prescription drugs; 5. Those who are pregnant or breastfeeding; 6. Those with any conditions that may affect the prognosis of healing; 6. Patients with a surgical duration of more than 45 minutes should also be excluded.

Design outcomes

Primary

MeasureTime frame
Swelling measurement;

Secondary

MeasureTime frame
Trismus measures;Pain measurements;Postoperative Symptom Severity Scale (PoSSe Scale);Healing Index;Oral Health Impact Scale;

Countries

China

Contacts

Public ContactLibin Zhou

Affiliated Stomatological Hospital of Guangzhou Medical University

fmmumario@126.com+86 20 8197 8293

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 3, 2026