- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06189768
A Study on Pigmentation Disorders in Children
January 4, 2024 updated by: Abal Baral, Nepal Health Research Council
A Retrospective Study on Pigmentation Disorders in Children in a Tertiary Care Children's Hospital.
The descriptive cross-sectional study was undertaken at Kanti Children's Hospital during the period from January 2020 to June 2021.
Ethical approval for the study was obtained from the Institutional Review Board of Kanti Children's Hospital (IRB-KCH).
The refence number is 59/2020-021.
The study focused on children with hyperpigmentation disorders presenting at the Dermatology Outpatient Department of Kanti Children's Hospital.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
299
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Kathmandu, Nepal
- Kanti Children's Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Inclusive of children ranging from newborns to 15 years old with hyperpigmentation due to any cause, the study excluded those admitted to wards with alternative diagnoses
Description
Inclusion Criteria:
- children ranging from newborns to 15 years old with hyperpigmentation due to any cause
Exclusion Criteria:
- children admitted to wards
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Children with hyperpigmentation disorder
Children aged 0 to 15 with hyperpigmentation due to any cause presenting to Dermatology Outpatient Department of Kanti Children's Hospital
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Measure the age distribution of children with hyperpigmentation disorders
Time Frame: 1.5 years
|
The age (in years) of all the children with hyperpigmentation disorders presenting to the outpatient department of Kanti Children's Hospital was recorded.
Outpatient hospital records were used for collecting the study variable.
|
1.5 years
|
Measure the gender distribution of children with hyperpigmentation disorders
Time Frame: 1.5 years
|
The gender (male or female) of all the children with hyperpigmentation disorders presenting to the outpatient department of Kanti Children's Hospital was recorded.
Outpatient hospital records were used for collecting the study variable.
|
1.5 years
|
Measure the caste distribution of children with hyperpigmentation disorders
Time Frame: 1.5 years
|
The caste of all the children with hyperpigmentation disorders presenting to the outpatient department of Kanti Children's Hospital was recorded.
Outpatient hospital records were used for collecting the study variable.
|
1.5 years
|
Measure the causes of hyperpigmentation in children aged 0 to 15
Time Frame: 1.5 years
|
Measure the prevalence of different causes of hyperpigmentation due to any cause in children aged 0 to 15 years presenting to the dermatology outpatient department of Kanti Children's Hospital.
Outpatient hospital records were used for collecting the study variables.
|
1.5 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2020
Primary Completion (Actual)
June 1, 2021
Study Completion (Actual)
June 1, 2021
Study Registration Dates
First Submitted
December 13, 2023
First Submitted That Met QC Criteria
December 30, 2023
First Posted (Actual)
January 5, 2024
Study Record Updates
Last Update Posted (Estimated)
January 8, 2024
Last Update Submitted That Met QC Criteria
January 4, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 59/2020-021
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.
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