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NCT07674264Recruiting

Cross-System Effects of Acute Intermittent Hypercapnia-Based Interventions in PD

A Pilot Study of Acute Intermittent Hypercapnia-Based Interventions on Upper Airway and Axial Motor Function in Parkinson's Disease

Source: ClinicalTrials.gov · Last updated 21 Aug 2026

Brief summary (registry, in English)

Parkinsonism impairs upper airway and axial motor control, leading to disordered breathing, reduced speech volume, and ineffective cough. Symptoms are poorly addressed by current therapies. This randomized pilot trial tests whether a single session of acute intermittent hypercapnic hypoxia (AIHH) or hypercapnic normoxia (AIHN) improves upper airway and axial motor function in Parkinsonism, and explores biomarker correlates of intervention responsiveness.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
32 (estimated)
First submitted
16 Jun 2026
Start date
12 Aug 2026
Primary completion date
31 Dec 2028
Lead sponsor
University of Florida
NCT number
NCT07674264

What you commit to

  • Study type: Interventional
  • Planned participants: 32
  • From 12 Aug 2026 to the primary completion date, 31 Dec 2028
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • additional neurologic conditions
  • severe illness or infection, including respiratory/cardiovascular/lung disease, or uncontrolled hypertension
  • history of head/neck/lung cancer with the exception of basal cell carcinoma
  • has deep brain stimulation electrodes implanted or has a history of deep brain stimulation

Age

  • pregnancy due to unknown tAIH effects on a fetus, although females of childbearing age will not be excluded\*

Other

  • inspiratory stridor
  • cigarette smoking or vaping within 5 years
  • is currently participating in another research study that could influence the results from this study
  • faints or becomes lightheaded at the sight of blood
    • If a female of childbearing potential indicates there is a chance she could be pregnant, she will be provided a pregnancy test and allowed to continue in the study if negative. This is because the fetal risks associated with intermittent hypoxia are unknown.

Who the study is looking for

  • adults 40 to 75 years of age (the latter to reduce the likelihood of cardiovascular disease)
  • diagnosis of idiopathic Parkinsonism with Hoehn and Yahr stages 2-4
  • medically stable with physician clearance
  • ability to ambulate at least 10 feet with/without assistance
  • ability to follow directions
  • willing to abstain from blood donation for the duration of the study

Age in the registry: 40 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Florida
Coordinator of this site? Confirm its status
GainesvilleUnited StatesRecruiting
Norman Fixel Institute for Neurological Diseases
Coordinator of this site? Confirm its status
GainesvilleUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.