Adjunctive Kinesiotaping in Surgical Treatment of Impacted Mandibular Third Molars

Medical University of Silesia

Status: Completed

Conditions: Impacted Third Molar Tooth

Treatments: Other: Kinesiotaping; Procedure: extraction of impacted third lower molar

Study type: Interventional

Funder types: Other

Identifiers

NCT07333963

BNW/NWN/0052/KB1/57/I/23

Details and patient eligibility

About

PATIENT INFORMATION SHEET Participants are invited to take part in a clinical study involving surgical removal of an impacted lower wisdom tooth. Participation in this study is entirely voluntary.

The purpose of this study is to observe the healing process after wisdom tooth removal and to assess whether the use of elastic therapeutic tape placed on the skin (kinesiotaping) may support recovery.

SURGICAL PROCEDURE The procedure will be performed under local anesthesia and will include: - Administration of local anesthesia

• Incision of the gum
• Exposure of the impacted tooth and surrounding bone
• Removal of the tooth
• Cleaning of the surgical site - Placement of sutures After the surgery, standard post■operative instructions will be provided. STUDY PROCEDURE

After the surgical procedure, patients will be randomly assigned to one of two groups:

1. Standard post■operative care
2. Post■operative care combined with application of elastic therapeutic tape on the skin of the face and neck area If the participants are assigned to the tape group, the tape will be applied immediately after surgery by qualified medical personnel and will remain in place for several days.

FOLLOW■UP VISITS Participant will be asked to attend follow■up visits on specific days after the procedure to allow the medical team to assess healing. PAIN MANAGEMENT Participant will be allowed to take pain medication if necessary, following medical advice.

VOLUNTARY PARTICIPATION Participation in this study is voluntary. Participant may withdraw from the study at any time without giving a reason and without affecting participants medical care.

CONFIDENTIALITY All medical information collected during the study will be handled confidentially and used solely for research purposes.

Enrollment: 70 patients

Sex: All

Ages: 16 to 64 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• No systemic diseases (generally healthy patient)

Indication for surgical extraction of impacted lower third molars for:

orthodontic reasons

surgical reasons

prophylactic reasons

Age between 16 and 64 years

Written informed consent to participate in the study

Exclusion criteria

• Presence of chronic systemic diseases, including:

diabetes mellitus

hypertension

autoimmune diseases

Pharmacological treatment in the period preceding the surgery

Pregnancy

Substance abuse or dependence

Head and neck malignancies

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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70 participants in 2 patient groups

Research group

Experimental group

Description:

Group undergoing Kinesiotaping after the surgical procedure

Treatment:

Procedure: extraction of impacted third lower molar

Other: Kinesiotaping

Control Group

Other group

Description:

no kinesiotaping

Treatment:

Procedure: extraction of impacted third lower molar