Hertel Exophthalmometry Values in Mexican Adults (HERTEL-MX)
Hertel Exophthalmometry Values in Mexican Adults and Their Association With Demographic Factors and Systemic Diseases
調査の概要
詳細な説明
Background: Hertel exophthalmometry is the most commonly used method for measuring globe protrusion in clinical practice. Normal exophthalmometric values vary according to ethnicity, sex, age, and craniofacial anatomy; therefore, population-specific reference values are necessary for accurate clinical interpretation. Currently, normative data for Mexican adults are limited.
Objective: To establish normative Hertel exophthalmometry values in Mexican adults and to evaluate their association with demographic characteristics and systemic diseases.
Methods: This is a prospective observational study. Adult participants attending the Ophthalmology Department will be consecutively recruited after providing written informed consent. Hertel exophthalmometry measurements will be obtained using a standardized technique by trained examiners. Demographic information, including age and sex, as well as relevant medical history and systemic diseases, will be recorded. The primary outcome is the distribution of Hertel exophthalmometry values in the study population. Secondary analyses will assess associations between exophthalmometric measurements and demographic or systemic variables.
Expected Significance: The study will provide normative Hertel exophthalmometry values for the Mexican adult population and identify factors associated with physiological variations in globe protrusion. These findings may improve the clinical evaluation of patients with suspected orbital disease and facilitate interpretation of Hertel exophthalmometry measurements in routine ophthalmic practice.
研究の種類
入学 (推定)
連絡先と場所
研究連絡先
- 名前:Roberto Ramirez Hernandez, MD, Ophthalmologist
- 電話番号:+525525137712
- メール:robert.rami.rr@gmail.com
研究場所
-
-
Mexico City
-
Mexico City、Mexico City、メキシコ、94806
- 募集
- ✔ Instituto de Oftalmología Fundación Conde de Valenciana IAP
-
コンタクト:
- Roberto Ramirez Hernandez
- 電話番号:5525137712
- メール:robert.rami.rr@gmail.com
-
-
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
サンプリング方法
調査対象母集団
説明
Inclusion Criteria:
- Adults aged 18 years or older.
- Mexican participants or individuals who self-identify as Mexican.
- Ability to understand the study procedures and provide written informed consent.
- Ability to undergo bilateral Hertel exophthalmometry.
- Participants with or without previously diagnosed systemic diseases.
Exclusion Criteria:
- Active thyroid eye disease
- History of orbital trauma or orbital fracture.
- Previous orbital surgery, orbital decompression, or surgery that may alter globe position.
- Presence or history of an orbital tumor, orbital inflammation, or orbital infection.
- Craniofacial abnormalities or facial asymmetry that may interfere with Hertel exophthalmometry.
- Ocular or eyelid conditions that prevent accurate positioning or measurement with the Hertel exophthalmometer.
- Inability to cooperate with the examination or obtain a reliable exophthalmometry measurement.
研究計画
研究はどのように設計されていますか?
デザインの詳細
コホートと介入
グループ/コホート |
介入・治療 |
|---|---|
|
Mexican Adult Participants
Adult Mexican participants undergoing standardized Hertel exophthalmometry and collection of demographic and medical history information for the establishment of normative exophthalmometric values and evaluation of associated factors.
|
Standardized bilateral Hertel exophthalmometry performed using a Hertel exophthalmometer to measure globe protrusion.
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Hertel Exophthalmometry Value
時間枠:At baseline
|
Bilateral Hertel exophthalmometry measurements (millimeters) obtained using a standardized Hertel exophthalmometer.
Normative values will be estimated and summarized for the study population.
|
At baseline
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- HERTEL-MX-2026-01
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。