Skip to content

Hilotherapy vs. Kinesio Taping in Orthognathic Surgery Recovery

Comparison of the Effects of Hilotherapy and Kinesio Taping on Edema, Pain, and Trismus After Orthognathic Surgery

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07006610
Enrollment
36
Registered
2025-06-05
Start date
2024-09-15
Completion date
2025-07-15
Last updated
2025-06-05

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

Conditions

Orthognathic Surgery, Postoperative Edema, Postoperative Pain, Trismus

Keywords

Hilotherapy, Kinesio Taping, Orthognathic Surgery, Postoperative Complications, Postoperative Recovery

Brief summary

This prospective randomized controlled trial aims to compare the effects of kinesio taping and hilotherapy on postoperative edema, pain, and trismus in patients undergoing bimaxillary orthognathic surgery.

Detailed description

Orthognathic surgery frequently causes postoperative edema, pain, and trismus. The study compares two adjunctive therapies: kinesio taping and hilotherapy. Forty-four patients without systemic disease, undergoing Le Fort I + BSSRO, will be randomly assigned to two groups. Group 1 will receive kinesio taping for 5 days. Group 2 will undergo hilotherapy for 48 hours. Pain (VAS), trismus (mouth opening), and edema (measured by both tape and 3D scanner) will be assessed at multiple postoperative time points. The goal is to determine the more effective intervention for postoperative recovery.

Interventions

DEVICEKinesio Tex® Gold Taping

Elastic kinesio tape applied postoperatively to the facial region and left in place for 5 days.

DEVICEHilotherm® Facial Cooling System

A polyurethane facial mask delivering continuous +17°C water cooling for 48 hours post-surgery.

Sponsors

Medipol University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Patients scheduled to undergo bimaxillary orthognathic surgery (Le Fort I + BSSRO) * Age between 18 and 50 years * No systemic disease * Voluntary participation with signed informed consent

Exclusion criteria

* Presence of systemic disease or immunosuppressive medication * Known allergy to kinesio tape * Inability to attend follow-up appointments * Facial anatomical deformities preventing measurement

Design outcomes

Primary

MeasureTime frameDescription
Change in Facial EdemaBaseline (Post-op 1.hour) and Post-op Days 1, 2, 5, 10, and 30Facial edema will be measured using both linear tape-based anthropometric measurements and 3D facial scanning at specified time points. Measurements will include tragus-to-ala, tragus-to-pogonion, and other standard facial distances.

Secondary

MeasureTime frameDescription
Change in Pain Score (VAS)Baseline(Post-op 1.hour) and Post-op Days 1, 2, 5, 10, and 30 |Pain will be assessed using a 10-point Visual Analog Scale (VAS), with 0 indicating no pain and 10 indicating the worst imaginable pain.
Change in Trismus (Maximum Mouth Opening)Baseline(Post-op 1.hour) and Post-op Days 1, 2, 5, 10, and 30Trismus will be assessed by measuring maximum interincisal distance using a millimeter ruler.

Countries

Turkey (Türkiye)

Contacts

Primary ContactOzge Sen, PhD Student
ozge.sen@std.medipol.edu.tr+905392179460

Outcome results

None listed

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