RECRUITING

Treatment of Sleep Apnea in Patients With Cervical Spinal Cord Injury

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This study will investigate potential therapeutic approaches for sleep-disordered breathing (SDB) in patients with chronic cervical spine injury (\>6 months post-injury).

Official Title

Treatment of Sleep Apnea in Patients With Cervical Spinal Cord Injury

Quick Facts

Study Start:2017-06-09

Study Completion:2024-06-30

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT02922894

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.

Ages Eligible for Study:18 Years to 89 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:Yes

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
1. healthy adults between the ages of 18 - 89 2. chronic spinal cord injury patients (T6 and above), \> 3 months since injury and not on mechanical ventilation, and have not received mechanical ventilation via tracheostomy in the past.	1. subjects ≤ 17 yrs old 2. Pregnant and lactating females 3. History of head trauma that resulted in neurological symptoms or loss of consciousness 4. advanced heart, lung, metabolic, liver or chronic kidney disease. 5. severe obstructive or restrictive respiratory defect by PFTs or history of tracheostomy 6. extreme obesity defined for this protocol as BMI ≥ 40 kg/m2 (to avoid the effect of morbid obesity on ventilation).

Inclusion Criteria

Exclusion Criteria

1. healthy adults between the ages of 18 - 89
2. chronic spinal cord injury patients (T6 and above), \> 3 months since injury and not on mechanical ventilation, and have not received mechanical ventilation via tracheostomy in the past.

1. subjects ≤ 17 yrs old
2. Pregnant and lactating females
3. History of head trauma that resulted in neurological symptoms or loss of consciousness
4. advanced heart, lung, metabolic, liver or chronic kidney disease.
5. severe obstructive or restrictive respiratory defect by PFTs or history of tracheostomy
6. extreme obesity defined for this protocol as BMI ≥ 40 kg/m2 (to avoid the effect of morbid obesity on ventilation).

Contacts and Locations

Study Contact

M Safwan Badr, M.D.

CONTACT

313-576-3548

m.badr@va.gov

Principal Investigator

M Safwan Badr, M.D.

PRINCIPAL_INVESTIGATOR

John D. Dingell VA Medical Center

Study Locations (Sites)

John D. Dingell VA Medical Center

Detroit, Michigan, 48201

United States

Collaborators and Investigators

Sponsor: John D. Dingell VA Medical Center

M Safwan Badr, M.D., PRINCIPAL_INVESTIGATOR, John D. Dingell VA Medical Center

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 Registration Dates

Study Start Date2017-06-09

Study Completion Date2024-06-30

Study Record Updates

Study Start Date2017-06-09

Study Completion Date2024-06-30

Terms related to this study

Additional Relevant MeSH Terms

Sleep Apnea
Spinal Cord Injury