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NCT01895998 · ClinicalTrials.gov registry record · Phase 1

Quantifying the Presence of Lung Disease and Pulmonary Hypertension in Children With Sickle Cell Disease

A Phase 1 study, sponsored by Duke University.

Completed
Registry status
Phase 1
Development phase
5
Enrollment target

NCT01895998: Completed Phase 1 study, sponsored by Duke University.

NCT01895998 is a Phase 1 study that has completed, run by Duke University. The registered enrollment target is 5 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01895998, a Phase 1 study, has completed, sponsored by Duke University.

COMPLETED
Registry status
Phase 1
Development phase
5 participants
Enrollment target

Study Summary

The proposed research study is a cross-sectional study enrolling young children with sickle cell disease between 5 and 12 years of age. They will be screened as outpatients for consent to perform pulmonary function testing (PFT) and echocardiography. In addition, the degree of bronchodilator response will be assessed at each session. To estimate presence of pulmonary hypertension, echocardiography will be performed at the time of PFT measures. Study Design: 1. Enroll children aged 5 to 12 years of age with sickle cell disease (HbSS, HbSC, HbS beta plus thalassemia, HbS beta zero thalassemia, and HbS OArab) who are established patients within the Duke Pediatric Sickle Cell Clinic. 2. Perform a chart review of all enrolled subjects to obtain specific details regarding birth history, nutritional status (weight, height), family history, sickle cell genotype, parental smoking history, recent laboratory parameters, parental smoking history, any concurrent conditions (atopy, asthma, airway anomaly), history of sickle cell complications and prescribed medications. 3. Perform spirometry and plethysmography with the administration of albuterol. 4. Before or after completion the PFT session, the patient will have echocardiography in the PFT lab area 5. Using medical record information, determine number of hospitalizations for any pulmonary symptoms indicative of acute chest syndrome (ACS) (dyspnea, fever, wheezing, hypoxia, cough, chest pain). In addition, we will track any respiratory or cardiac symptoms or therapies for each subject 6 years after enrollment up to age 18 years using the registry. 6. As standard of care, refer any child identified as having lung disease or pulmonary hypertension to a pediatric pulmonologist and/or cardiologist for monitoring, treatment and ongoing care.

Primary Outcome

Obstructive lung disease will be defined as forced expiratory volume in 1 second (FEV1), or forced vital capacity (FVC) \< 80% predicted based on normative data for age, sex, height, weight and race. Restrictive lung disease will be defined as total lung capacity (TLC) \<80% predicted based on normative data for age, sex, height, weight and race.

Interventions

  • DRUG Albuterol

Trial Details

FieldValue
Enrollment Target 5 participants
Start Date 2013-08
Est. Completion 2014-04
Phase Phase 1
Duke University

1,725 total trials

What the finished NCT01895998 record still lists

NCT01895998 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 5 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 1 intervention - of which Albuterol is the first listed.

NCT01895998 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01895998 about?

NCT01895998 is a clinical study titled "Quantifying the Presence of Lung Disease and Pulmonary Hypertension in Children With Sickle Cell Disease". The proposed research study is a cross-sectional study enrolling young children with sickle cell disease between 5 and 12 years of age. They will be screened as outpatients for consent to perform pulmonary function testing (PFT) and echocardiography. In addition, the degree of bronchodilator respons...

What is the current status of trial NCT01895998?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 5 participants. The study started on 2013-08. Estimated completion is 2014-04.

What interventions are being tested in trial NCT01895998?

The interventions under investigation include: Albuterol (DRUG).

Who is sponsoring clinical trial NCT01895998?

This trial is sponsored by Duke University, which has 1,725 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01895998's enrollment target sits among peer trials

5 1989th of 2000 higher than 6 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01895998, the US trial registry maintained by the National Library of Medicine. NCT01895998 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.