Adjunctive Kinesiotaping in Surgical Treatment of Impacted Mandibular Third Molars

NCT ID: NCT07333963

Last Updated: 2026-01-12

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 70 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-05-14
• Study Completion Date: 2025-12-08

Brief Summary

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.

Conditions

Impacted Third Molar Tooth

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: NONE

Study Groups

Research group

Group undergoing Kinesiotaping after the surgical procedure

Group Type: EXPERIMENTAL

Kinesiotaping

Intervention Type: OTHER

basic lymphatic KT application

extraction of impacted third lower molar

Intervention Type: PROCEDURE

basic surgical extraction

Control Group

no kinesiotaping

Group Type: OTHER

extraction of impacted third lower molar

Intervention Type: PROCEDURE

basic surgical extraction

Interventions

Kinesiotaping

basic lymphatic KT application

Intervention Type: OTHER

extraction of impacted third lower molar

basic surgical extraction

Intervention Type: PROCEDURE

Eligibility Criteria

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

• Minimum Eligible Age: 16 Years
• Maximum Eligible Age: 64 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Medical University of Silesia

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Uniwersyteckie centrum stomatologii

Bytom, Silesian Voivodeship, Poland

Countries

Poland

Other Identifiers

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

Identifier Type: -

Identifier Source: org_study_id