Pharmacologic Induction of Tolerance for Hypoxia & Hypothermia

Hypoxia Clinical Trial

— PhITHy-Ho  

Official title:

Pharmacologic Induction of Tolerance for Hypoxia & Hypothermia

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06129825
• Other study ID #: HP-00108068
• Status: Not yet recruiting
• Start date: December 1, 2024
• Est. completion date: July 30, 2026

Study information

• Verified date: January 2024
• Source: University of Maryland, Baltimore
• Contact: Allan Doctor, MD
• Phone: 314-791-0297
• Email: Adoctor[@]som.umaryland.edu
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Warfighter Performance Optimization in Extreme Environments remains an area of important and intense investigation, with the following goals: (1) Optimize, sustain and augment medical readiness and physiological/ psychological performance in extreme and hazardous military operational environments and (2) develop joint DoD countermeasures and guidance to sustain performance, assess physiological status, and reduce injury risk in extreme and hazardous operational environments. Successful and safe outcomes in extreme and hazardous operational environments require that warfighters maintain optimum cognitive and exercise performance during physiologic stress. Extreme environmental conditions encountered in such environments include warfighter exposure to hypoxia and hypothermia, alone or in combination. Both hypoxia and hypothermia undermine O2 delivery system homeostasis, imposing dangerous constraints upon warfighter cognitive and exercise capacity. While red blood cells (RBCs) are commonly recognized as O2 transport agents, their function as a key signaling and control node in O2 system delivery homeostasis is newly appreciated. Through O2 content-responsive modulation of RBC energetics, biomechanics, O2 affinity and control of vasoactive effectors in plasma - RBCs coordinate stabilizing responses of the lung, heart, vascular tree and autonomic nervous system - in a fashion that maintains O2 delivery system homeostasis in the setting of either reduced O2 availability (hypobaric hypoxia) or increased O2 demand (hypothermia). Human RBCs demonstrate adaptive responses to exercise, hypoxia and hypothermia - these changes are commonly appreciated as a key element enabling high altitude adaptation. However, under conditions of hypoxia and hypothermia, without prior adaptation, RBC performance is adversely impacted and limits the dynamic range of stress adaptation for O2 delivery homeostasis - therefore limiting warfighter exercise capacity and cognitive performance in extreme environments, such as during acute mountain sickness.

Description:

The investigator's strategy is to: (a) repurpose approved drugs with potential for salutary effect upon RBC performance attributes that contribute to O2 delivery homeostasis during stress and (b) efficiently identify lead candidates through sequential evaluation in relevant and rigorous benchtop and in vivo models that include examination for gender-specific effects. Our assay platforms are selected to characterize RBC physiology relevant to O2 delivery, with focus upon RBC O2 affinity, energetics, biomechanics, vascular interaction and control of regional blood flow. The investigator will sample RBC suspensions serially (0, 1,3h) and quantify the RBC performance attributes across the range of modeled environmental extremes, defining RBC performance constraint as > 20% impairment in each attribute and determine pharmacologic rescue (defined as > 20% improvement in each attribute) using mixed model RM-ANOVA, as a function of gender. The investigator will power analysis to 80% at a<5%; based on our published data with these assays and experience, this requires 10-15 subjects/group. Drug candidates with evidence of PhIT-HyHo potential will advance to in vivo screening, prioritized by the number of RBC attributes rescued per drug. Specific description of our approach to evaluate each RBC performance attribute follows. RBC performance attributes will be quantified under controlled conditions (Temperature: 28 - 37°C; pO2: 50 - 100 Torr, alone and in combination in our temperature-controlled thin film tonometer38 (NB temperature simulates hypothermic body temperature): (a) glycolytic flux, (b) resilience to oxidative stress, (c) deformability & aggregation, (d) O2 affinity and Bohr effect, (e) vasoactivity.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 50
• Est. completion date: July 30, 2026
• Est. primary completion date: December 1, 2025
• Gender: All
• Age group: 18 Years to 88 Years

Eligibility

Inclusion Criteria:

• Subject is >/= 18years of age.
• Subject weighs a minimum of 110lbs
• Subject must be generally healthy individual

Exclusion Criteria:

• Suspected or diagnosed with ongoing (chronic) or acute infection
• Pregnant
• Non-English speaking
• Ages 89 and over

Related Conditions & MeSH terms

• Altitude Sickness
• Hypothermia
• Hypoxia
• Mountain Sickness

Intervention

Other:
• Prospective
Single arm, healthy adult volunteers for blood donation.

Locations

Country	Name	City	State
n/a

Sponsors (2)

Lead Sponsor	Collaborator
University of Maryland, Baltimore	United States Department of Defense

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Drug candidate effects on RBC deformability and aggregation.	RBC deformability will be assessed by ektacytometry and Brillouin microscopy. Measurements will include elongation index (ability of RBC's to elongate as a function of shear) in addition to a non-shear assessment of RBC deformability. Aggregation will be assessed by syllectometry.	18-24months
Other	Drug candidate effects on RBC 02 affinity and Bohr effect.	This will be assessed using the HEMOX analyzer and thin film tonometry (with gas mix blending) to determine hemoglobin p50 shift (i.e., the partial pressure of oxygen at which hemoglobin is 50% saturated with oxygen) and the ability of hemoglobin O2 affinity to respond to pH.	18-24months
Other	Drug candidate effects on RBC 02 vasoactivity.	RBC's will be tested in a bio-assay containing aortic tissue to determine their dilatory capacity under hypoxia and their constriction properties under normoxia.	18-24months
Primary	Drug candidate effects on RBC energy metabolism	The Investigator will specifically focus on relative glycolytic and pentose phosphate pathway flux, to determine robustness of RBC antioxidant capacity. Flux analysis will be performed by metabolomics (mass spectrometry).	18-24months
Secondary	Drug candidate effects on RBC resilience to oxidative stress.	The Investigator will assess robustness of RBC antioxidant systems following in vitro incubation in an oxidative environment. Outcome measures will include the ability of RBC's to scavenge oxidants including superoxide and hydrogen peroxide, RBC lysis and oxidative changes in RBC membrane proteins.	18-24months