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The Improvement of Neuro-sensory Disturbance in Patients Underwent Orthognathic surgery Following physiotherapy

The Improvement of Neuro-sensory Disturbance in Patients Underwent Orthognathic surgery Following TENS (Electrical Nerve Stimulation) physiotherapy

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210224050492N1
Enrollment
54
Registered
2023-01-17
Start date
2022-12-22
Completion date
Unknown
Last updated
2023-02-07

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

Conditions

the improvement of sensory-neural changes in orthognathic surgery patients. Dentofacial anomalies [including malocclusion]

Interventions

Intervention 1: Intervention group: Patients with class 3 skeletal deformity and in need of bimaxillary orthognathic surgery were selected and TENS (Electrical Nerve Stimulation) physiotherapy was per

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients undergoing orthosurgery treatments who have written consent to participate in the research.

Exclusion criteria

Exclusion criteria: Patients with a history of facial trauma Patients who have had a history of surgery in these areas. Patients who had a history of pathological lesions in the mandible or maxilla and underwent surgery. Patients who need re-surgery after orthosurgery. Patients who suffer from Bad Split during surgery. Patients who, due to the treatment plan during surgery, the mandible osteotomy method is not the same on both sides. Patients with a history of brain or neurological problems. Patients with a history of taking drugs due to mental problems

Design outcomes

Primary

MeasureTime frame
Therapeutic modalities. Timepoint: 6 months after surgery. Method of measurement: view.;VAS (Visual Pain Scale). Timepoint: 6 months after surgery. Method of measurement: According to patients' self-reported estimates.;Brush Stroke Test. Timepoint: 6 months after surgery. Method of measurement: Patients' feeling.;Two-point discrimination test. Timepoint: 6 months after surgery. Method of measurement: The patient's feeling of colon diagnosis.

Secondary

MeasureTime frame
Two-point discrimination test. Timepoint: 6 months after surgery. Method of measurement: The Patients' feeling of colon diagnosis.;Brush Stroke Test. Timepoint: 6 months after surgery. Method of measurement: patients' feeling.;VAS (Visual Pain Scale). Timepoint: 6 months after surgery. Method of measurement: According to patients' self-reported estimates.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMeysam Mohammadi khah

Shahid Beheshti University of Medical Sciences

shahreyar333@gmail.com+98 21 2240 3075

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026