- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06047418
Blepharoptosis in Indonesia: A 5-Year Multicenter Study on Characteristics and Surgical Evaluation
Blepharoptosis in Indonesia: A 5-Year Retrospective Cross-Sectional Multicenter Study on Characteristics and Surgical Evaluation
The goal of this observational study is to learn about blepharoptosis cases in national referral hospitals in Indonesia. The main questions it aims to answer are:
- How is the clinical characteristics, types, and surgical evaluations of blepharoptosis in this particular setting
Participant who include in this study is a patient diagnosed with blepharoptosis cases and complete medical history from January 2016 to December 2020 across 10 tertiary hospitals in Indonesia from 5 provinces
Study Overview
Status
Intervention / Treatment
Detailed Description
The research obtained data from the medical records of 823 patients across 10 tertiary hospitals in Indonesia from 5 provinces including Cipto Mangunkusumo Hospital (Jakarta), JEC Eye Hospitals & Clinics (Jakarta), Mohammad Hoesin Hospital, Saiful Anwar Hospital, Cicendo Hospital, Sanglah Hospital, M Djamil Hospital, Wahidin Sudirohusodo Hospital, Sardjito Hospital, Kariadi Hospital, and Soetomo Hospital. Inclusion criteria entailed fully completed patient data, while exclusion criteria encompassed duplicated patient data across different years.
Patient demographic data, encompassing gender, age, and ethnicity, were extracted from the collected data. Age was divided into two groups: children (0-18 years) and adults (19-40 years, and ≥40 years). This investigation incorporated pediatric participants to assess the occurrence of blepharoptosis in children, prompted by a study revealing an 8.0% prevalence of childhood blepharoptosis.8 In age-specific relative incidence of blepharoptosis, aponeurotic and myogenic ptosis was the majority in patients younger than 40 years, emphasizing the significant association between older age and blepharoptosis prevalence, hence a cut-off of 40 years was used.7 Patient blepharoptosis classifications were established according to etiology, dividing cases into congenital and acquired categories. Acquired instances encompassed diverse etiologies (myogenic, aponeurotic, mechanical, neurogenic, traumatic, and pseudoptotic ptosis). Physical examinations discerned specific blepharoptosis traits, categorizing types as unilateral (palpebral fissure asymmetry >1 mm) and bilateral (marginal reflex distance (MRD) >2mm in both eyes).9 Levator muscle function (LF) assessment classified into excellent (≥13 mm), good (8 to 11 mm), fair (5.0 to 7 mm), and poor (≤4 mm). Severity was gauged as mild (MRD ≤2 mm), moderate (MRD 3-4mm), or severe (MRD ≥ 4mm).10 For surgical outcome evaluation, analysis depended on surgical method, success rate, and complications, divided into recurrence requiring re-operation, undercorrection, overcorrection, lagophthalmos, and asymmetry. Utilizing SPSS Statistics 25, the study employed Chi-square or Fisher's exact test and logistic regression to explore variable relationships. Initially, odds ratios were determined with bivariate analysis to examine the raw relationship between each independent variable and the outcome, without any control for other variables. Furthermore, we also computed odds ratios with multivariate analysis, which consider the simultaneous effect of multiple variables on the outcome. For this purpose, we used the stepwise method. The adequacy of our logistic regression model was assessed using the Hosmer and Lemeshow Test. A non-significant result from the Hosmer and Lemeshow Test (p>0.05) indicates that our model's predictions match the observed outcomes, suggesting that the model fits the data well.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
DKI Jakarta
-
Jakarta Pusat, DKI Jakarta, Indonesia, 10430
- Cipto Mangunkusumo hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- patients diagnosed with blepharoptosis
- complete medical record history
Exclusion Criteria:
- duplication of previously inputted cases
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Demographic and Clinical Characteristic
Time Frame: 2021-2022
|
demographics were categorised into sex, age and race while clinical characteristic were including type of ptosis, laterality, mechanism, severity, elevator function.
we use percentage to calculate the proportion of the patients
|
2021-2022
|
|
Surgical technique
Time Frame: 2021-2022
|
we collect the data history of patient's eyes who were undergoing the surgery.
we use percentage to calculate the proportion of each surgical technique used as frontal suspension, levator resection, elevator advancement, fasanella servant, mullerectomy and tumor excision
|
2021-2022
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
surgical evaluations
Time Frame: 2021-2022
|
surgical evaluations were observed and calculated from the current complications appeared in percentage
|
2021-2022
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 21-03-0300
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Surgical Incision
-
Near East University, TurkeyCompletedCesarean Delivery Affecting Fetus | Incision, Surgical | Pfannenstiel Incision Length | Fetal Occipitofrontal DiameterTurkey
-
Diskapi Teaching and Research HospitalCompleted
-
Molnlycke Health Care ABSyntactxNot yet recruitingSurgical Wound | Surgical Incision | Surgical Wound Dehiscence | Incision, Surgical | Surgical Wound, Recent
-
Sarasota Memorial Health Care SystemMiMedx Group, Inc.Enrolling by invitationParathyroid Diseases | Surgical Incision | Incision | Thyroid; WoundUnited States
-
Columbia UniversityEthicon, Inc.CompletedEfficiency of Surgical Incision Closure | Post-operative ScarUnited States
-
The Metis FoundationCompletedIncisions, SurgicalUnited States
-
Stony Brook UniversityWithdrawn
-
Ethicon, Inc.CompletedSurgical IncisionsBelgium, Germany, Sweden, United Kingdom
-
Inonu UniversityCompletedSurgical IncisionTurkey
-
Instituto de Investigacion Sanitaria La FeMedtronicUnknown
Clinical Trials on Blepharoplasty
-
Medical University of ViennaCompleted
-
Benha UniversityUnknown
-
Instituto de Olhos de GoianiaCentro de Referência em OftalmologiaCompletedEfficacy of a Technique (Brassiere Sutures)
-
Benha UniversityUnknownEyelid DiseasesUnited Arab Emirates
-
Benha UniversityCompleted
-
Benha UniversityUnknownEyelid DiseasesUnited Arab Emirates
-
Marmara UniversityCompletedDry Eye | Meibomian Gland Dysfunction | Ocular Surface Disease | Brow Ptosis | Dermatochalasis of EyelidTurkey
-
Mersin Training and Research HospitalEnrolling by invitation
-
Benha UniversityRecruiting
-
Peking Union Medical CollegeCompletedWrinkle Appearance | Melanin HyperpigmentationChina