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Orthognathic SurgeryNCT07477873

Evaluation of Emotional Responses Using the I-Motions System and Self-assessment Questionnaires, and Assessment of Postoperative Anatomical and Structural Units (TMJ and Masticatory Muscles) in Orthognathic Surgery Patients

A study testing Observational Assessment in people with Orthognathic Surgery and Malocclusions, run by Lithuanian University of Health Sciences at 1 site in Lithuania.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

Orthognathic surgery is a surgical procedure involving one or both jaws to correct skeletal discrepancies, restore proper occlusion, and improve facial aesthetics. Individuals with dentofacial abnormalities often experience difficulties with chewing, biting, and social interaction, which may negatively impact… Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Observational Assessment
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
1 siteLithuania
Study dates
3 Mar 2026to 1 Sep 2028
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients treated at the Lithuanian University of Health Sciences (LSMU) Kaunas Clinics Department of Maxillofacial Surgery.
  • Diagnosed according to the internal registry of Kaunas Clinics with one of the following ICD-10 codes:
  • K07.0 - Major abnormalities of jaw size K07.1 - Abnormalities of jaw-cranial base relationship K07.2 - Abnormalities of dental arch relationship K07.4 - Malocclusion, unspecified K07.5 - Functional disorders of teeth and face K07.8 - Other dentofacial anomalies K07.9 - Dentofacial anomaly, unspecified
  • Scheduled to undergo planned orthognathic surgery.
  • Classified as American Society of Anesthesiologists (ASA) physical status I or II.
  • Age ≥ 18 years.
  • Able and willing to provide written informed consent.

Who cannot join

  • Refusal or inability to provide informed consent.
  • Planned orthognathic surgery combined with additional elective surgical procedures (e.g., rhinoplasty, blepharoplasty, or other cosmetic procedures).
  • Age under 18 years.
  • Reinterventions or revision orthognathic surgery.
  • Emergency surgical procedures.
  • Known allergy to local anesthetics, anti-inflammatory drugs, or opioids.
Show all 9Show fewer
  • Diagnosed anxiety and/or depression requiring pharmacological treatment.
  • Presence of psychiatric disorders classified under ICD-10 Chapter F (Mental and Behavioral Disorders).
  • Pregnancy.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Lithuania1 site
  • Lithuanian University of Health Sciences, Departments of maxillofacial surgery, Kaunas Clinics

    Kaunas, Kauno, 50161

Other trials in Lithuania

About this study

Orthognathic surgery is a surgical procedure involving one or both jaws to correct skeletal discrepancies, restore proper occlusion, and improve facial aesthetics. Individuals with dentofacial abnormalities often experience difficulties with chewing, biting, and social interaction, which may negatively impact psychological well-being and overall quality of life.

Orthognathic surgery must be combined with orthodontic treatment before and after the operation to ensure optimal functional and aesthetic outcomes. The conventional "orthodontics-first" approach involves prolonged preoperative orthodontic treatment (typically 12-24 months, sometimes up to 48 months) to decompensate dental alignment and reveal the true skeletal discrepancy prior to surgery. Although effective for achieving stable occlusion, this method is time-consuming and may temporarily worsen facial aesthetics and function during the preoperative phase.

Read more

The "surgery-first" approach eliminates or significantly reduces preoperative orthodontics, performing surgery first followed by postoperative orthodontic treatment. This method shortens overall treatment time, provides immediate aesthetic improvement, facilitates favorable orthodontic tooth movement, and may lead to earlier improvement in conditions such as obstructive sleep apnea. It is generally recommended for patients with mild anterior crowding, minimal transverse discrepancies, a flat or mild curve of Spee, and normally inclined incisors. Common surgical techniques include genioplasty, bilateral sagittal split osteotomy (BSSO), oblique ramus osteotomy, and Le Fort I osteotomy. Whenever possible, procedures are performed intraorally to avoid visible scarring.

Orthognathic surgery induces not only anatomical and functional changes but also psychological adaptations. Soft tissues, masticatory muscles, and the temporomandibular joint (TMJ) adapt to new skeletal relationships, contributing to improved facial balance and patient self-perception. However, there is currently no unified diagnostic algorithm to comprehensively evaluate postoperative anatomical, physiological, and socio-emotional changes. Emotional satisfaction, TMJ structural changes, muscle strength variations, sleep quality, and pain outcomes remain insufficiently studied.

The study proposes two hypotheses: the null hypothesis (H0) assumes no postoperative changes in TMJ anatomy, masticatory muscle strength, emotional response, facial pain, sleep quality, or depressive characteristics; the alternative hypothesis (H1) assumes that such changes do occur.

The objectives are to evaluate masticatory muscle strength and structure, TMJ anatomical changes, emotional state, depression and anxiety predisposition, sleep quality, facial pain, and aesthetic perception before and after surgery.

The study will include up to 100 patients undergoing bimaxillary orthognathic surgery (with or without genioplasty) at the Lithuanian University of Health Sciences Kaunas Clinics. Assessments will be conducted preoperatively, immediately postoperatively, and 3-6 months after surgery. Methods include CBCT imaging for TMJ evaluation, electromyography for masseter muscle strength, emotional analysis using the iMotions platform (facial expression analysis and electrodermal activity), and validated questionnaires (PHQ-15, HADS, VAS). Strict ethical standards will be followed in accordance with international guidelines, with informed consent obtained from all participants. No additional financial costs or conflicts of interest are declared.

The expected outcome is to determine correlations between anatomical, functional, psychological, and aesthetic changes following orthognathic surgery, providing a more comprehensive understanding of patient satisfaction and overall quality-of-life improvement.

Read the detailed description

Orthognathic surgery is the surgical treatment of one or both jaws by osteotomy of the bones in order to correct the malalignment/abnormal shape of the jaws, to restore their relationship to the central occlusion, thus restoring a correct bite and restoring the correct facial shape.

Individuals with dentofacial abnormalities struggle with biting and chewing, social interactions, and peer pressure to alter their look. Due to these difficulties, these people may suffer from psychological issues and see a marked decline in their quality of life.

Orthognathic surgery is a specialized procedure that must be carried out with orthodontic treatment. This means that before and after the surgical intervention, orthodontic care is essential to align the teeth and jaws, ensuring optimal results properly. The combination of these treatments helps correct misalignments, improve bite function, and enhance facial aesthetics. Without orthodontic preparation and follow-up, the surgical correction alone would not be as effective in achieving a stable and harmonious outcome.

Conventional approach

The term "orthodontic first approach" refers to the conventional method used in treatment, where orthodontic procedures are initiated before any surgical intervention. To achieve a stable surgical occlusion and overcome postoperative occlusal instability, preoperative orthodontic therapy is carried out before orthognathic surgery to realign the maxilla and mandible and to disclose the true skeletal disparity before surgery. The attractive profile of the face and the function of the teeth gradually deteriorate throughout the preoperative phase due to dental decompensation. Preoperative orthodontic therapy has the major disadvantage of being time-consuming. It typically takes 12 to 24 months, but depending on the complexity of the patient's initial oral condition, it may take up to 48 months.

Surgery-first approach

The surgery-first technique refers to an approach in which orthognathic surgery is performed first, followed by postoperative orthodontic therapy, without the need for preoperative orthodontic treatment. The modified surgery technique is used when the preoperative orthodontic treatment duration is reduced to less than six months. The benefits of the surgery-first method includes a reduction in the overall duration of treatment, a favorable postoperative orthodontic direction (which is the same as the direction of natural compensation), early facial aesthetic improvement, and early obstructive sleep apnea correction.

The surgery-first strategy is typically recommended for patients who require less prior care, such as those with:

  1. well-aligned to mildly crowded anterior teeth;
  2. a flat to mild curve of Spee;
  3. normal to mildly proclined or retroclined incisors;
  4. a minimal transverse discrepancy.

These days, genioplasty, bilateral sagittal split osteotomy (BSSO) of the mandible, oblique ramus osteotomy of the mandible, and Le Fort I osteotomy of the maxilla are the most commonly performed surgical procedures for correcting dentofacial abnormalities, with some variations. For optimal safety, jaw osteotomies should be performed through an intraoral approach whenever possible. This technique helps prevent facial scarring while ensuring adequate exposure of the skeletal structures. Important structures need to be maintained, and postoperative nutrition needs to be taken into account.

Orthognathic surgery affects many changes that occur in the human body and even the psychological aspects of a patient's personality.

The shape and appearance of the face are not corrected, as during orthognathic surgery the soft tissues, masticatory muscles, and the temporomandibular joint (TMJ) adjust/adapt to the changed bone positions and the altered bite and inter-maxillary relationships, thus correcting and creating a balanced facial appearance/contour that allows the person to feel more complete and emotionally attractive to themselves.

Medical research has not yet developed a unified diagnostic and assessment algorithm to fully evaluate post-operative changes after orthognathic surgery. The socio-emotional component and emotional satisfaction of patients after these operations have not been assessed. Physiological changes in the masticatory muscles and the TMJ after surgery are not assessed. Post-operative emotional and physiological pain was not assessed.

HYPOTHESIS

H0: Following orthognathic surgery, patients will not experience any changes in their temporomandibular joint anatomical structures, masticatory muscle strength, emotional response, facial pain, sleep quality before or after the procedure, or depressed characteristics.

H1: Following orthognathic surgery, patients will experience changes in their temporomandibular joint anatomical structures, masticatory muscle strength, emotional response, facial pain, sleep quality, before or after the procedure, or depressed characteristics.

OBJECTIVES

  1. To assess the strength of patients' masticatory muscle contraction and their structures before and after orthognathic surgery.
  2. To assess the predisposition to depression and anxiety in patients scheduled for orthognathic surgery and the reasons for the onset or disappearance of these predispositions.
  3. To determine and assess the quality of sleep before and after surgery.
  4. To assess the emotional state of patients on the I-Motions platform before and after surgery.
  5. To assess post-operative acute and chronic pain with the Visual Analogue Scale (VAS) and the I-Motions platform to determine its origin.
  6. To evaluate the postoperative changes in the temporomandibular joint (TMJ) anatomic structures in terms of their significance for the success of the surgery, the patient's overall life satisfaction, aesthetics, and the occlusal relationship.

MATERIALS and METHODS

Study design

Following the approval of the Ethical Committee of LSMU Kaunas Clinics' Center and the National Ethical Committee of Lithuania, informed consent was obtained from each patient enrolled in the study. Initially, a comprehensive patient evaluation was conducted (as detailed below) for individuals undergoing orthognathic surgery, including mandibular, maxillary, or bimaxillary procedures, with or without genioplasty. Subsequently, a postoperative evaluation was performed. The study aims to enroll up to 100 patients.

After the first phase of orthodontic treatment the patient will be reevaluated and CBCT scan will be performed for the planning of orthognathic surgery. Main surgeon which performs all orthognathic surgical procedures according to his license will evaluate all CBCT scans. CBCT scan is minimally invasive for patient health and it is required in all steps of the surgery. By performing this study no extra scans will be done.

One day before the orthognathic surgery:

  1. Patients will fill in the General Data Questionnaire (gender, age, education, etc.);
  2. A non-invasive study using electromyography on the i-Motions platform for emotional assessment (i-Motions 8.2, i-Motions A/S, Copenhagen, Denmark) will be implemented. This equipment uses an integrated artificial intelligence-based facial expression analysis algorithm (Affdex 4.0, Affectiva, Boston, USA) and electrodermal activity modules (Shimmer3 GSR, Shimmer, Dublin, Ireland) to provide a detailed and comprehensive characterization of the respondents' emotional state and the physiological galvanic skin response.
  3. A non-invasive study using electromyography for m.masseter straight evaluation will be implemented with i-Motions platform;
  4. Patients will fill Patient Health Questionnaire-15 (PHQ-15) for assessing somatic symptoms severity;
  5. Patients will fill Hospital Anxiety and Depression Scale (HADS) for assessing depression and anxiety symptoms;
  6. Facial aesthetics will be assessed.
  7. Visual Analogue Scale (VAS) for preoperative pain in masticatory system.

After the orthognathic surgery:

  1. Visual Analogue Scale (VAS) will be performed.
  2. A CBCT scan will be performed.

After soft tissue recovery (3-6 months):

  1. A non-invasive study using electromyography on the i-Motions platform for emotional assessment will be performed again;
  2. A non-invasive study using electromyography on the i-Motions platform for m.masseter strength;
  3. Patient Health Questionnaire-15 (PHQ-15) for assessing somatic symptoms severity;
  4. Hospital Anxiety and Depression Scale (HADS) for assessing depression and anxiety symptoms;
  5. Facial aesthetics assessed.
  6. CBCT scan for TMJ anatomic/bone structures area changes evaluation.

Population

In Europe, including Lithuania, there is a lack of statistical data regarding the number of orthognathic surgeries performed; therefore, it is not possible to determine the exact number of potential subjects. This study aims to recruit the maximum feasible number of participants.

The study includes patients of Lithuanian University of Heath Sciences Kaunas Clinics Department of Maxillofacial surgery according to the following diagnoses in the internal register of Kaunas Clinics who are planned to undergo orthognathic surgery:

K07.0 Major abnormalities of jaw size; K07.1 Abnormalities of the relationship between the jaws and the base of the skull; K07.2 Abnormalities of the dental arch relation; K07.4 Malocclusion, unspecified; K07.5 Functional disorders of teeth and face; K07.8 Other anomalies of teeth and face; K07.9 Anomaly of teeth and face, unspecified;

The criteria for subject selection are as follows. The inclusion criterion is patients undergoing scheduled bimaxillary surgery with or without genioplasty, ASA 1 or 2. The exclusion criteria are: refusal to participate in the study, patients scheduled for bimaxillary surgery together with another complementary surgical procedure (such as rhinoplasty, blepharoplasty), age < 18 years, reinterventions, urgent surgeries, allergies to local anesthetics, allergies to anti-inflammatories, allergies to opioids, pregnant women, patients with diagnosed anxiety and depression, taking medication.

Intervention After the initial orthodontic treatment, orthognathic surgery is planned. One of the phases of the planning process is a CBCT scan. We will use CBCT scan to evaluate the anatomical structures of the TMJ.

One day before surgery, the patient will be asked to fill with the General Data Questionnaire, PHQ-15, HADS, a non-invasive study using electromyography on the iMotions platform for emotional assessment, electromyography for m.masseter straight and weight evaluation, facial aesthetics evaluation, VAS.

After the orthognathic surgery VAS will be performed again, a CBCT scan will be performed to evaluate operation.

After soft tissue recovery (3-6 months): electromyography on the iMotions platform for emotional assessment and m.masseter strength, PHQ-15, HADS, facial aesthetics evaluation, CBCT scan for TMJ anatomic/bone structures area changes evaluation.

Ethics

Prior to making a decision regarding participation in the study, all necessary information will be provided to each patient.

The information disclosed will be in strict accordance with the ethical principles outlined in the Declaration of Helsinki (latest revision at the 64th General Assembly, Fortaleza, Brazil, October 2013) and the International Council for Harmonisation Good Clinical Practice (ICH-GCP) Guidelines.

Before the commencement of the study, formal approval will be obtained from the Lithuanian Regional Ethics Committee for Biomedical Research.

The researcher will comprehensively outline the measures implemented to safeguard patient data and privacy, ensuring full compliance with European Directive 95/46/EC, the General Data Protection Regulation (EU) 2016/679, and Organic Law 3/2018 of December 5 on the Protection of Personal Data and the Guarantee of Digital Rights. Additionally, the researcher will elucidate the study's potential risks, inherent limitations, and the patient's right to withdraw at any stage without repercussions on their medical care or relationship with the research team.

Each patient will be provided with a detailed written information sheet and an informed consent document, accompanied by a verbal explanation. Written consent must be obtained before initiating any study-related procedures.

Financial report

This study is not subject to additional costs, since all the necessary data, software and surgical techniques are in the Lithuanian University of Heath Sciences Kaunas Clinics Department of Maxillofacial surgery and no additional procedures are introduced.

Disclosure of financial information

  • The researchers state that there is no financial transaction involved in the study;
  • The authors declare not to have any interest conflicts.

Expected results

By utilizing a novel algorithm, the I-Motions platform, and validated questionnaires, this study aims to analyze the correlation between depression, anxiety, and perceived changes in appearance before and after orthognathic surgery. The primary objective is to assess patient satisfaction, psychological and lifestyle changes, factors influencing the decision to undergo orthognathic surgery, and alterations in anatomical structures, including the masticatory muscles and TMJ, sleep quality and emotional response.

Being tested
Observational Assessment
Keywords
Orthognathic surgery, Dentofacial deformities, Bimaxillary surgery, Temporomandibular joint (TMJ), Masticatory muscle strength, Masseter electromyography, Depression and anxiety, Hospital Anxiety and Depression Scale (HADS), Quality of life, Visual Analogue Scale (VAS), iMotions platform
Medical subject headings
Malocclusion, Jaw Abnormalities, Dentofacial Deformities, Sleep Initiation and Maintenance Disorders, Anxiety Disorders, Depression

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Observational AssessmentOther

    Prospective assessment of anatomical, functional, and psychological changes before and after standard orthognathic surgery.

Study groups in NCT07477873
Study groupRoleWhat they receive
Bimaxillary Orthognathic Surgery PatientsExperimentalPatients undergoing planned orthognathic surgery (with or without genioplasty) with preoperative and postoperative functional, anatomical, and psychological assessment.
Receives: Other: Observational Assessment

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Temporomandibular Joint (TMJ) Anatomical Structures After Orthognathic Surgery

    Assessment of preoperative and postoperative changes in temporomandibular joint anatomical structures using cone-beam computed tomography (CBCT), including evaluation of condylar position and joint space measurements.

    Measured: Baseline (1 day before surgery) and 3-6 months after surgery

Secondary outcomes (5)
  1. Change in Masseter Muscle Strength After Orthognathic Surgery

    Evaluation of masseter muscle contraction strength using electromyography (EMG) before and after surgery.

    Measured: Baseline and 3-6 months after surgery

  2. Change in Depression and Anxiety Symptoms

    Hospital Anxiety and Depression Scale (HADS), a 14-item questionnaire with scores ranging from 0 to 21 for each subscale, where higher scores indicate greater anxiety or depressive symptoms.

    Measured: Baseline and 3-6 months after surgery

  3. Change in Emotional Response Measured by iMotions Platform

    Evaluation of emotional state using facial expression analysis (Affdex) and electrodermal activity via iMotions platform.

    Measured: Baseline and 3-6 months after surgery

  4. Change in Facial Pain Intensity

    Facial pain intensity will be assessed using the Visual Analogue Scale (VAS), a 10-cm scale ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain.

    Measured: Baseline and immediate postoperative period

  5. Change in Sleep Quality After Orthognathic Surgery

    Sleep quality will be assessed using the Pittsburgh Sleep Quality Index (PSQI), a self-reported questionnaire consisting of 19 items with a global score ranging from 0 to 21, where higher scores indicate poorer sleep quality.

    Measured: Baseline and 3-6 months after surgery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Mar 2026
  2. Study start3 Mar 2026 (estimated)
  3. Primary completion1 Sep 2028 (estimated)
  4. Study completion1 Sep 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Diagnosis
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07477873
Sponsor's protocol ID
BE-2-133
Status last verified
Mar 2026
First submitted
11 Mar 2026
Last updated
17 Mar 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Publications

  • World Medical Association. World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects. JAMA. 2013 Nov 27;310(20):2191-4. doi: 10.1001/jama.2013.281053. No abstract available.

    PubMed 24141714
  • Tiret L, Hatton F, Desmonts JM, Vourc'h G. Prediction of outcome of anaesthesia in patients over 40 years: a multifactorial risk index. Stat Med. 1988 Sep;7(9):947-54. doi: 10.1002/sim.4780070906.

    PubMed 3175394
  • Yamada K, Hanada K, Hayashi T, Ito J. Condylar bony change, disk displacement, and signs and symptoms of TMJ disorders in orthognathic surgery patients. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2001 May;91(5):603-10. doi: 10.1067/moe.2001.112153.

    PubMed 11346742
  • Ruggiero F, Borghi A, Bevini M, Badiali G, Lunari O, Dunaway D, Marchetti C. Soft tissue prediction in orthognathic surgery: Improving accuracy by means of anatomical details. PLoS One. 2023 Nov 27;18(11):e0294640. doi: 10.1371/journal.pone.0294640. eCollection 2023.

    PubMed 38011187
  • Mazzaferro DM, Wes AM, Naran S, Pearl R, Bartlett SP, Taylor JA. Orthognathic Surgery Has a Significant Effect on Perceived Personality Traits and Emotional Expressions. Plast Reconstr Surg. 2017 Nov;140(5):971-981. doi: 10.1097/PRS.0000000000003760.

    PubMed 29068935
  • Monson LA. Bilateral sagittal split osteotomy. Semin Plast Surg. 2013 Aug;27(3):145-8. doi: 10.1055/s-0033-1357111.

    PubMed 24872760
  • Ahmadvand A, Alavi S, Mehraban SH. An overview of surgery-first orthognathic approach: History, indications and limitations, protocols, and dentoskeletal stability. Dent Res J (Isfahan). 2021 Jun 22;18:47. eCollection 2021.

    PubMed 34429867
  • Choi JW, Lee JY. Current concept of the surgery-first orthognathic approach. Arch Plast Surg. 2021 Mar;48(2):199-207. doi: 10.5999/aps.2020.01305. Epub 2021 Mar 15.

    PubMed 33765739
  • Cariati P, Martinez R, Martinez-Lara I. Psycho-social impact of orthogathic sugery. J Clin Exp Dent. 2016 Dec 1;8(5):e540-e545. doi: 10.4317/jced.53007. eCollection 2016 Dec.

    PubMed 27957267
  • Khechoyan DY. Orthognathic surgery: general considerations. Semin Plast Surg. 2013 Aug;27(3):133-6. doi: 10.1055/s-0033-1357109.

    PubMed 24872758

Questions about this trial

What is this clinical trial studying?

A study testing Observational Assessment in people with Orthognathic Surgery and Malocclusions, run by Lithuanian University of Health Sciences at 1 site in Lithuania.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 17 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Lithuania. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Temporomandibular Joint (TMJ) Anatomical Structures After Orthognathic Surgery (time frame: Baseline (1 day before surgery) and 3-6 months after surgery). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07477873, which also lists 10 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Mar 2026.

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