Management of Postoperative Complications After Mandibular Third Molar Extraction Using Submucosal Triamcinolone Injection, Kinesiology Taping, and Standard Care

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-40
SponsorAllama Iqbal Medical College

About this trial

The surgical removal of impacted lower wisdom teeth (mandibular third molars) frequently leads to uncomfortable postoperative symptoms, including pain, facial swelling (edema), and restricted jaw movement (trismus). This study aims to evaluate and compare the effectiveness of two different treatment strategies alongside standard care to reduce these complications.

A total of 60 patients undergoing surgical extraction will be randomly assigned to one of three groups: Group A will receive a local submucosal injection of 10mg Triamcinolone (a corticosteroid), Group B will have Kinesiology Tape applied to the face to enhance fluid drainage, and Group C will receive standard postoperative care alone. Patient recovery outcomes, including pain levels, facial swelling, and jaw mobility, will be monitored and measured at 24 hours, 3 days, and 7 days after the surgery. The study's primary objective is to determine if adding either a pharmacological injection or a mechanical tape significantly improves patient recovery compared to standard postoperative care alone.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients aged 18-40 years

Surgical patients requiring extraction of Impacted mandibular third molars

Disqualifiers

Known allergy to corticosteroids/adhesive

Systemic diseases

Active infection

Pregnancy and lactation

Trial design

Design model

Parallel

Treatments tested in this trial

  • Triamcinolone Acetonide 10mg

    Drug

    Single local submucosal injection of 10mg Triamcinolone Acetonide administered immediately after third molar surgical extraction.

  • Kinesiology Taping

    Device

    Elastic kinesiology tape applied over the masseteric region immediately after surgery to assist in tissue decompression and lymphatic flow.

  • Standard Postoperative Care

    Other intervention

    Standard pharmacological regimen (routine oral analgesics/antibiotics) and post-operative home-care instructions.

Treatment groups

60 Participants
are divided into 3 treatment groups
Group A: Group A (Triamcinolone + Standard Care)Experimental treatment 2 interventions
Group B: Group B (Kinesiology Taping + Standard Care)Experimental treatment 2 interventions
Group C: Group C (Standard Care Alone)Other 1 intervention

Trial outcomes

Primary outcomes

1

Postoperative Pain Severity

Postoperative pain severity will be assessed using a 10-point Visual Analog Scale (VAS), where 0 indicates "no pain" and 10 indicates "the worst pain imaginable

Time frame
Preoperatively (baseline), and at 24 hours, 3 days, and 7 days postoperatively

Secondary outcomes

1

Postoperative Facial Swelling (Edema)

Postoperative facial swelling will be assessed using quantitative facial measurements in millimeters (using standard landmark reference points like tragus to corner of the mouth, tragus to soft tissue pogonion, and lateral canthus to gonion)

Time frame
Preoperatively (baseline), and at 24 hours, 3 days, and 7 days postoperatively
2

Postoperative Trismus

Postoperative trismus (limited mouth opening) will be quantified in millimeters by measuring the maximum interincisal distance at maximum active mouth opening using a digital vernier caliper

Time frame
Preoperatively (baseline), and at 24 hours, 3 days, and 7 days postoperatively.

Other outcomes

Sponsors and contacts

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