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A New Optical Sweat Test Method Based on a Citric Acid-derived Multi-halide Sensor

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Penn State Health

Status

Terminated

Conditions

Cystic Fibrosis

Treatments

Diagnostic Test: Measurement of Sweat Chloride and Sweat Bromide

Study type

Interventional

Funder types

Other

Identifiers

NCT03367494
00008612

Details and patient eligibility

About

Cystic Fibrosis (CF) is a hereditary multi-system disease affecting approximately 30,000n children and adults in the USA. The diagnosis of CF requires biochemical confirmation (either abnormal sweat chloride measurement and/or identification of two CF disease causing mutations) plus clinical symptomatology. Measurements of sweat chloride remain cumbersome and although most common methodology to confirm CF diagnosis with limitations especially in young children less than 6 months of age and in areas that lack ability for the complex testing. The study objectives of this current research proposal include: A) To expand upon previously obtained pilot study data "Evaluation of a fluorescent-based chloride sensor as an optical sweat test to diagnose cystic fibrosis" B) To add the exploratory measurement of sweat Bromide as a first in human assessment observation, C) To Evaluate the development of smartphone based point-of-care technology for chloride and bromide sensor measurements, D) To further expand the class of citrate-based sensors with improved fluorescence and sensing properties for the design of new fluorescence-based analytical and diagnostic solutions based on the automated multi-halide detection system, and E) To develop point-of-care systems that can successfully integrate into clinical settings to improve current practices and facilitate early detection of disease.

Enrollment

25 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adults 18 years of age or older capable of providing written informed consent AND
  • Patients with an established diagnosis of Cystic Fibrosis (CF) OR Healthy volunteers

Exclusion criteria

  • Participants under medications or with disorders known to cause a positive error in the sweat test will be excluded in the study. Common causes of positive error in sweat test are mineralocorticoid hormone therapy, adrenal insufficiency, glycogen storage diseases, hypothyroidism, hypoparathyroidism, nephrogenic diabetes insipidus, G6PD deficiency or ectodermal dysplasia OR
  • Any other skin or soft tissue disorders that could affect obtaining the necessary volumes of sweat.

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

25 participants in 2 patient groups

Subjects with Cystic Fibrosis
Other group
Description:
Diagnostic
Treatment:
Diagnostic Test: Measurement of Sweat Chloride and Sweat Bromide
Healthy Volunteers
Other group
Description:
Diagnostic
Treatment:
Diagnostic Test: Measurement of Sweat Chloride and Sweat Bromide

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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