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Study Evaluating the Effect of a Specific Trace Metal Complex Versus Placebo on the Severity of Apnea in Patients With Obstructive Sleep Apnea Syndrome (OLIGO-SAS)

Primary Purpose

Apnea, Obstructive

Status
Not yet recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Nutri PNEA
Placebo
Sponsored by
Laboratoires Pronutri
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Apnea, Obstructive focused on measuring trace elements, obstructive sleep apnea

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: adult patient with moderate to severe sleep apnea-hypopnea syndrome confirmed by polysomnography dating less than 3 months with an apneas/hypopneas index ≥ 15 events/h stable weight (5% variation of the weight at the time of the polysomnography done within 3 months) Exclusion Criteria: patient previously treated for OSA by continuous positive airway pressure or mandibular orthosis obesity (body mass index > 30 kg/m2) pregnant or post-pregnancy women less than 6 months old or of childbearing age without an effective method of contraception respiratory, cardiac, hepatic or renal failure active cancer or history of cancer alcohol abuse antidepressant intake use of compression stockings intake of product or supplementation enriched with trace metals and/or trace elements and/or mineral salts and/or vitamins. taking any type of psychotropic medication previous intake of trace elements to treat OSA

Sites / Locations

  • Laboratoire EFCR - CHU de Grenoble

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Trace elements

Placebo

Arm Description

Nutri PNEA in a single dose (4 sequences of 10 tablets). Nutri PNEA is a complex of trace elements with the status of a food supplement.

4 sequences of 10 tablets containing only excipients

Outcomes

Primary Outcome Measures

Change in the number of apneas/hypopneas

Secondary Outcome Measures

Change in Ventilatory Response
Change in Ventilatory Response assessed by tests of Ventilatory Response to Carbon Dioxide (CO2)
Proportion of patients with a 50% reduction in the apnea-hypopnea index
AHI is used to diagnose obstructive sleep apnea by counting respiratory events. An index greater than 5 per hour defines a ventilatory disorder. AHI defines severity as well, the index is: Mild, between 5 and 15 per hour Moderate, between 15 and 30 per hour Severe, over than 30 per hour
Proportion of patients with an apnea-hypopnea index < 30/hour
AHI is used to diagnose obstructive sleep apnea by counting respiratory events. An index greater than 5 per hour defines a ventilatory disorder. AHI defines severity as well, the index is: Mild, between 5 and 15 per hour Moderate, between 15 and 30 per hour Severe, over than 30 per hour
Proportion of patients with an apnea-hypopnea index < 15/hour
AHI is used to diagnose obstructive sleep apnea by counting respiratory events. An index greater than 5 per hour defines a ventilatory disorder. AHI defines severity as well, the index is: Mild, between 5 and 15 per hour Moderate, between 15 and 30 per hour Severe, over than 30 per hour
Change in sleep quality
Sleep quality will be assessed by the Pittsburgh Sleep Quality Index (PSQI) questionnaire. This will be used to measure sleep quality over the last 60 days.The self-related questions include the assessment of seven different sleep domains : sleep quality, sleep latency , sleep duration , habitual sleep efficiency, sleep disturbances , use of sleeping medications , and daytime dysfunction .The seven components scores are then added to yield a global PSQI score in the range of zero to 21. The higher the score, the worse the sleep quality. A global score greater than five is diagnostic of poor sleep quality.
Change in sleepiness
Sleepiness will be assessed by the Epworth Sleepiness Scale (ESS).It will be used to measure daytime sleepiness .It can determine the chance of falling asleep in 8 different circumstances. ESS score can range from 0 to 24. A global score greater than ten is diagnostic of excessive daytime sleepiness .

Full Information

First Posted
February 19, 2023
Last Updated
March 5, 2023
Sponsor
Laboratoires Pronutri
Collaborators
Clin-Experts
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1. Study Identification

Unique Protocol Identification Number
NCT05758324
Brief Title
Study Evaluating the Effect of a Specific Trace Metal Complex Versus Placebo on the Severity of Apnea in Patients With Obstructive Sleep Apnea Syndrome
Acronym
OLIGO-SAS
Official Title
Prospective, Randomized, Double-blind, Parallel-group Study Evaluating the Effect of a Specific Trace Metal Complex Versus Placebo on the Severity of Apnea in Patients With Obstructive Sleep Apnea Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
March 1, 2023 (Anticipated)
Primary Completion Date
January 31, 2024 (Anticipated)
Study Completion Date
January 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Laboratoires Pronutri
Collaborators
Clin-Experts

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Obstructive sleep apnea syndrome (OSA) is defined by the association of clinical symptoms - drowsiness in particular - and sleep breathing disorders, objectified by measuring the apnea-hypopnea index (AHI). Apneas and hypopneas during sleep are responsible for micro-arousals and hypoxemia. In the short term, these result in daytime sleepiness with reduced alertness, difficulty driving and carrying out tasks (increased risk of road accidents and accidents at work), memory and concentration problems. , mood disorders. These disturbances lead to an impairment of the quality of life. In the long term, severe OSA (AHI > 30 events/hour) increases all-cause mortality and cardiovascular morbidity. The reference treatment is nasal ventilation by Continuous Positive Airway Pressure (CPAP). In practice, the observance and effectiveness of CPAP are limited by the sometimes difficult acceptance of cumbersome equipment, involving noise pollution and requiring the wearing of night-time equipment that some patients find difficult to bear. The alternative treatment is represented by the mandibular advancement orthosis . Lifestyle and dietary measures are always recommended. To date, no pharmacological treatment has demonstrated its effectiveness in OSA. Studies have shown that the antioxidant capacity of the blood is reduced in patients with OSA. It would be secondary to the cycles of hypoxia and reoxygenation which cause a modification of the oxidative balance, leading to an increase in free radicals. It has been observed that the serum levels of trace elements and heavy metals are higher during OSA, by deterioration of the balance of these substances due to oxidative stress and inflammation. Antioxidant therapies have reduced biomarkers of oxidative stress in apneic patients. A new path of research is opening up with the use of antioxidants and trace elements in OSA. To scientifically support the hypothesis of the action of these supplements based on trace metals on OSA, PRONUTRI wish to conduct a comparative, randomized, double-blind study versus placebo evaluating the effect of a specific complex of trace metals in the OSA.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Apnea, Obstructive
Keywords
trace elements, obstructive sleep apnea

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
42 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Trace elements
Arm Type
Experimental
Arm Description
Nutri PNEA in a single dose (4 sequences of 10 tablets). Nutri PNEA is a complex of trace elements with the status of a food supplement.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
4 sequences of 10 tablets containing only excipients
Intervention Type
Dietary Supplement
Intervention Name(s)
Nutri PNEA
Intervention Description
4 sequences of 10 tablets (one intake)
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
4 sequences of 10 tablets (one intake)
Primary Outcome Measure Information:
Title
Change in the number of apneas/hypopneas
Time Frame
60 days
Secondary Outcome Measure Information:
Title
Change in Ventilatory Response
Description
Change in Ventilatory Response assessed by tests of Ventilatory Response to Carbon Dioxide (CO2)
Time Frame
60 days
Title
Proportion of patients with a 50% reduction in the apnea-hypopnea index
Description
AHI is used to diagnose obstructive sleep apnea by counting respiratory events. An index greater than 5 per hour defines a ventilatory disorder. AHI defines severity as well, the index is: Mild, between 5 and 15 per hour Moderate, between 15 and 30 per hour Severe, over than 30 per hour
Time Frame
60 days
Title
Proportion of patients with an apnea-hypopnea index < 30/hour
Description
AHI is used to diagnose obstructive sleep apnea by counting respiratory events. An index greater than 5 per hour defines a ventilatory disorder. AHI defines severity as well, the index is: Mild, between 5 and 15 per hour Moderate, between 15 and 30 per hour Severe, over than 30 per hour
Time Frame
60 days
Title
Proportion of patients with an apnea-hypopnea index < 15/hour
Description
AHI is used to diagnose obstructive sleep apnea by counting respiratory events. An index greater than 5 per hour defines a ventilatory disorder. AHI defines severity as well, the index is: Mild, between 5 and 15 per hour Moderate, between 15 and 30 per hour Severe, over than 30 per hour
Time Frame
60 days
Title
Change in sleep quality
Description
Sleep quality will be assessed by the Pittsburgh Sleep Quality Index (PSQI) questionnaire. This will be used to measure sleep quality over the last 60 days.The self-related questions include the assessment of seven different sleep domains : sleep quality, sleep latency , sleep duration , habitual sleep efficiency, sleep disturbances , use of sleeping medications , and daytime dysfunction .The seven components scores are then added to yield a global PSQI score in the range of zero to 21. The higher the score, the worse the sleep quality. A global score greater than five is diagnostic of poor sleep quality.
Time Frame
60 days
Title
Change in sleepiness
Description
Sleepiness will be assessed by the Epworth Sleepiness Scale (ESS).It will be used to measure daytime sleepiness .It can determine the chance of falling asleep in 8 different circumstances. ESS score can range from 0 to 24. A global score greater than ten is diagnostic of excessive daytime sleepiness .
Time Frame
60 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: adult patient with moderate to severe sleep apnea-hypopnea syndrome confirmed by polysomnography dating less than 3 months with an apneas/hypopneas index ≥ 15 events/h stable weight (5% variation of the weight at the time of the polysomnography done within 3 months) Exclusion Criteria: patient previously treated for OSA by continuous positive airway pressure or mandibular orthosis obesity (body mass index > 30 kg/m2) pregnant or post-pregnancy women less than 6 months old or of childbearing age without an effective method of contraception respiratory, cardiac, hepatic or renal failure active cancer or history of cancer alcohol abuse antidepressant intake use of compression stockings intake of product or supplementation enriched with trace metals and/or trace elements and/or mineral salts and/or vitamins. taking any type of psychotropic medication previous intake of trace elements to treat OSA
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Louis PEPIN
Organizational Affiliation
University Hospital, Grenoble
Official's Role
Principal Investigator
Facility Information:
Facility Name
Laboratoire EFCR - CHU de Grenoble
City
Grenoble
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
MARIE JOYEUX-FAURE
First Name & Middle Initial & Last Name & Degree
Jean-Louis PEPIN, PhD

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Study Evaluating the Effect of a Specific Trace Metal Complex Versus Placebo on the Severity of Apnea in Patients With Obstructive Sleep Apnea Syndrome

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