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Decreasing Edema with Platysma Exercises Following Third Molar Extraction Surgery

Decreasing Edema with Platysma Exercises Following Third Molar Extraction Surgery: a Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06761664
Enrollment
31
Registered
2025-01-07
Start date
2024-07-17
Completion date
2024-11-04
Last updated
2025-01-08

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

Conditions

Third Molar Extraction

Keywords

Third molar extraction, Platysma muscle, Exercise, Edema

Brief summary

This study will investigate the effects of a platysma muscle exercise on edema following third molar extraction surgery.

Detailed description

The investigators hypothesized that, during the muscle contraction of the platysma, the vascular structures will be subjected to a pump effect, leading to an increase in venous circulation. Additionally, due to its connection to the fascia, the investigators propose that platysma contractions may mobilize the fascia and stimulate the lymph nodes, thereby improving interstitial fluid flow. This could lead to an effective treatment option for decreasing edema after third molar tooth extraction. Therefore, this study aims to investigate the effects of platysma exercises applied after third molar tooth extraction on edema while observing the differences on pain and trismus.

Interventions

OTHERPlatysma Exercise Group

The participants in this group will perform a platysma exercise for 7 days following third molar extraction surgery.

OTHERControl (Standard treatment)

Participants in this group will receive routine treatment following third molar extraction.

Sponsors

Gazi University
CollaboratorOTHER
Ankara University
CollaboratorOTHER
Melek Volkan Yazici
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Patients aged 18-40, * Those requiring impacted third molar extraction * Those with no systemic health conditions, were included in the study * Those who accepted to participate in the study

Exclusion criteria

* Those who had systemic diseases * Those who were taking medications that could interfere with inflammation, or healing, * Those who were pregnant or breastfeeding, * Those who had infections or pathologies involving teeth 38 and 48, * Those who were unable to comply with postoperative recommendations or required therapeutic interventions outside the study protocol

Design outcomes

Primary

MeasureTime frameDescription
Facial EdemaChange of facial edema from baseline to 7 daysEdema will be measured by taking five distinct facial measurements using a standard plastic tape measure (accuracy ±0.5 mm), ensuring the tape makes contact with the skin. The following measurements will be recorded: (a) the distance between the most posterior point of the tragus and the most lateral point of the lip commissure; (b) from the tragus to the chin mid point; (c) from the tragus to the lateral canthus of the eye; (d) from the lateral canthus to the lowest point of the mandibular angle; and (e) from the mandibular angle to the middle of the nasal bone.

Secondary

MeasureTime frameDescription
Pain following third molar extractionChange in pain scores from baseline to 7 daysPain will be assessed using a 100 mm visual analog scale. Patients will be asked to mark the point on the scale that best represented their level of pain. The scale ranges from 0, indicating no pain, to 10, representing the worst pain imaginable pain.
TrismusChange of trismus from baseline to 7 daysTrismus will be assessed by measuring the maximum inter-incisal distance using callipers to record the widest mouth opening.

Countries

Turkey (Türkiye)

Outcome results

None listed

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