Intensive Care (ICU)NCT07866625
An Investigation of The Relationship Between Muscle Mass, Physiological Parameters, and Blood Gas Levels in Adult Patients Hospitalized in The Intensive Care Unit
An observational study of Intensive Care (ICU), run by Ankara Yildirim Beyazıt University at 1 site in Turkey (Türkiye).
Trial summary
This study was designed to investigate the relationship between muscle mass and physiological parameters and blood gas values in adult patients admitted to the intensive care unit. Read more about this study
- Who is it for?
- Ages 18 hours and olderHealthy volunteers can take part
- Conditions the study is for
- Intensive Care (ICU)
- How many people
- 80 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 10 Dec 2025to 10 Dec 2026
- How long will I take part?
- 1 Day
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 hours and older
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: The study data will include adult patients hospitalized in the palliative care intensive care unit, the pulmonary intensive care unit, and the cardiovascular surgery intensive care unit at Erzurum City Hospital.
Who may be able to join
- Age: Adult patients aged 18 years and older Clinical unit: Patients admitted to palliative care, pulmonary intensive care, or cardiovascular intensive care units Length of stay: Patients expected to remain in the intensive care unit for at least 48 hours Physical eligibility: Patients with no conditions preventing the measurement of muscle mass Clinical stability: Patients without severe hemodynamic instability or active bleeding at the time of measurement Ethical compliance: Individuals who have volunteered to participate in the study and whose informed consent has been obtained from them or their legal representative
Who cannot join
- Patients with a history of previously diagnosed neuromuscular disorders (myasthenia gravis, Guillain-Barré syndrome, chronic polyneuropathies)
- Patients with severe renal or hepatic insufficiency that could directly affect muscle mass
- Presence of severe edema: Patients with a pitting edema score of 3+ or 4+ on the pitting edema test, or individuals with documented widespread edema in nursing or medical records
- Patients with an amputation, hematoma, or open wound on the extremity to be measured
- Pregnant patients
- Patients whose intensive care stay lasted less than 48 hours or for whom the measurement could not be completed due to discharge or death
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Turkey (Türkiye)1 site, 1 recruiting
- Recruiting
Erzurum City Hospital,
Erzurum
Sümeyye Karabacak
About this study
This study was designed to investigate the relationship between muscle mass and physiological parameters and blood gas values in adult patients admitted to the intensive care unit. While muscle mass will be determined using anthropometric measurements, SpO₂, pulse rate, blood pressure, diuresis, and arterial blood gas values will be evaluated. The primary hypothesis of the study is that there is a significant relationship between muscle mass and, in particular, oxygenation and other physiological and blood gas parameters.
Read the detailed description
Intensive care units are facilities where patients whose physiological balance has been disrupted due to life-threatening illnesses are monitored and treated. In these patients, critical illness disrupts homeostasis, affecting multiple organ functions; sepsis, prolonged mechanical ventilation, and immobilization are significant risk factors for ICU-acquired weakness . These conditions lead to a loss of muscle mass, which negatively affects metabolic reserve, respiratory muscle strength, and recovery capacity; prolongs the length of hospital stay; and increases the risk of mortality.
Muscle tissue not only enables movement but also plays a critical role in metabolic and systemic regulation through the secretion of myokines. Therefore, muscle loss is not limited to physical weakness but also affects metabolic and systemic functions .Muscle weakness is common in intensive care patients, and losses exceeding 10%-particularly in the first few weeks-are associated with functional impairments .
A decrease in muscle mass can weaken respiratory muscle strength, leading to reduced oxygen saturation, impaired circulatory function, and decreased organ perfusion; this may manifest as pulse variability, low oxygen saturation, and decreased urine output. In a study of patients intubated due to COVID-19-related pneumonia, it was observed that individuals with high muscle density had higher extubation success rates, lower complication rates, and reduced mortality. Similarly, post-discharge measurement of quadriceps muscle mass using BIA showed a positive correlation with long-term recovery.The relationship between muscle mass and respiratory function was examined using DXA, and significant associations were found between restrictive ventilatory dysfunction and muscle mass . These data indicate that muscle mass indirectly supports oxygenation and hemodynamic stability.
The risk of muscle loss increases with prolonged immobilization, mechanical ventilation, and the use of high doses of sedatives. For this reason, the assessment of muscle mass in intensive care patients is important both for monitoring clinical course and for investigating its relationship with physiological parameters such as SpO₂, blood pressure, pulse, diuresis, and blood gas values.
Following a review of the literature, no study was found that examined the relationship between anthropometric measurements of muscle mass and physiological parameters and blood gas values in adult patients admitted to the intensive care unit. In this context, the study was planned.
Type of Study: Observational Study Study Population: Patients admitted to the palliative care intensive care unit, pulmonary intensive care unit, and cardiovascular intensive care unit at Erzurum City Hospital will be included in the study.
Sample Size: In this study, as the primary analysis, the relationship between muscle mass and SpO₂ will be evaluated using a one-way Pearson correlation; similar studies in the literature have shown a moderate correlation (r ≈ 0.30) (Damanti et al., 2022; Lim et al., 2024).Under these assumptions, a power analysis conducted with a statistical power of (1-β) = 0.80 and a significance level of (α = 0.05) determined that a sample size of approximately 67 patients would be required to test the hypothesis that SpO₂ values increase as muscle mass increases. To account for potential data losses, the sample size was planned to be approximately 80 patients.
The criteria used in similar studies in the literature that examine the relationship between muscle mass, muscle strength, and clinical outcomes in intensive care patients will serve as the basis.
Collection of research data: The research data will include adult patients hospitalized in the palliative care, pulmonary, and cardiovascular surgery intensive care units at Erzurum City Hospital. Informed consent forms will be obtained from the patients or their first-degree relatives, as well as from the attending physician in the intensive care unit.
Edema Assessment: This is a routine measurement. It poses no risk to human health. Before measurements begin, patients' upper and lower extremities will be assessed for edema. The assessment will be based on the pitting edema test-performed by applying light pressure with the thumb for 2-3 seconds-and clinical observation. For edema assessment, measurements will be taken at the widest point on the medial surface of the calf, the anterior aspect of the thigh, the midpoint of the femur (midpoint of the SIAS and the patella), the anterior surface of the midpoint of the humerus (between the acromion and the olecranon), and the posterior surface of the midpoint of the humerus (between the acromion and the olecranon).
For grading: 0+: No indentation → No edema; 1+: Mild indentation, recovers quickly → Mild edema, 2+: Moderate indentation, persists for a few seconds → Moderate edema, 3+: Deep indentation, persists for up to 15 seconds → Severe edema, 4+: Very deep indentation, persists for >30 seconds → Very severe edema; these values will be used.
Anthropometric Measurements Patients' circumference measurements and skinfold measurements will be taken while they are lying on their backs. Muscles will be kept relaxed, and a non-elastic anthropometric tape and a Baseline brand skinfold caliper will be used. Measurements will be taken on the right side of the body whenever possible; if access is obstructed, the left or opposite side will be used, and this will be noted on the record form. All measurements will be taken in a single attempt and recorded with a precision of 0.1 mm. The researchers performing the measurements have received training in accordance with the ISAK protocol.
Circumference Measurements: Measurements will be taken at the calf, thigh, and biceps. For the calf, measurements will be taken at the widest point of the calf ; for the thigh, at the midpoint of the femur on the anterior aspect of the thigh and 10 cm above the patella; and for the biceps, from the midpoint of the humerus , and the results will be recorded in centimeters.
Skinfold Measurements: Measurements will be taken from the biceps, triceps, suprailiac region, abdomen, thigh, and calf. Biceps: measured vertically from the midpoint of the humerus; triceps: measured vertically from the midpoint between the acromion and the olecranon; suprailiac: measured obliquely just above the iliac crest; abdomen: measured vertically 2 cm to the right of the navel; thigh: measured vertically from the midpoint of the femur; calf: vertically from the widest point of the calf, and the measurements will be recorded in centimeters.
Measurements will not be taken from the subscapular region, as it is believed this would interfere with patient positioning.
Muscle Mass Calculation: The thigh cross-sectional area formula will be used to calculate muscle mass.
The muscle radius (r) will be determined using the formula: thigh circumference / 2.
Then, using π = 3.14, the formula for muscle cross-sectional area = π (r - (skinfold thickness / 2))² will be used.
Physiological Parameters and Blood Gases: On the day anthropometric measurements are taken, patients' SpO₂, pulse rate, blood pressure, and diuresis will be recorded.
In addition, arterial blood gas (ABG) values will be based on data obtained during routine clinical follow-up within ±12 hours of the measurement time; no additional blood samples will be drawn. Parameters to be recorded: pH, PaO₂, PaCO₂, SaO₂, HCO₃-, base excess (BE), lactate, as well as FiO₂ and ventilator parameters.
Measurement of diuresis: For patients with a urinary catheter: The urine volume collected in the urine bag over a 12-hour period or ±12 hours will be recorded. For patients without a urinary catheter: Urine output by the patient over a 12-hour period (using a soft catheter or urine bag) will be recorded. Unit: To be recorded as mL/12 hours.
All data will be used to evaluate the relationship between muscle mass and oxygen saturation, blood pressure, pulse, diuresis, and blood gas parameters in intensive care patients.
Statistical Analysis: The data obtained from this study will be analyzed using SPSS (The Statistical Package for the Social Sciences). The Shapiro-Wilk test will be used to determine whether the data are normally distributed. The Pearson test will be used for groups with a normal distribution, and the Spearman test will be used for groups without a normal distribution. Results will be evaluated at a significance level of 0.05.
.
- Conditions
- Intensive Care (ICU)
- Keywords
- Intensive Care, Muscle Mass, Anthropometric measurements, arterial kan gaze, Oxygen Saturation
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| patients in intensive care | patients in intensive care |
What is being measured
The primary outcome is the main question the study is designed to answer.
muscle mass
Measured: 10.12.2026
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Oct 2026
- Study start10 Dec 2025
- Primary completion10 Dec 2026 (estimated)
- Study completion10 Dec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (3)Papers the sponsor has linked to this study.
- Other trials for Intensive Care (ICU)Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Cross-sectional
- Enrolment
- 80 participants (estimated)
- Target duration
- 1 Day
Sponsor and investigators
- Lead sponsor
- Ankara Yildirim Beyazıt University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Bihter Aslanyurek, Ankara Yildirim Beyazıt University
- Investigators
- Bihter AKINOĞLU, Principal investigator, Ankara Yildiirm Beyazit UniversitySümeyye Karabacak, Study chair, Erzurum City Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07866625
- Sponsor's protocol ID
- AYBU-FTR-BA-12
- Status last verified
- Sep 2026
- First submitted
- 29 Sep 2026
- Last updated
- 8 Oct 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: all patient data
Publications
Damanti S, Cristel G, Ramirez GA, Bozzolo EP, Da Prat V, Gobbi A, Centurioni C, Di Gaeta E, Del Prete A, Calabro MG, Calvi MR, Borghi G, Zangrillo A, De Cobelli F, Landoni G, Tresoldi M. Influence of reduced muscle mass and quality on ventilator weaning and complications during intensive care unit stay in COVID-19 patients. Clin Nutr. 2022 Dec;41(12):2965-2972. doi: 10.1016/j.clnu.2021.08.004. Epub 2021 Aug 16.
PubMed 34465493Brodovicz KG, McNaughton K, Uemura N, Meininger G, Girman CJ, Yale SH. Reliability and feasibility of methods to quantitatively assess peripheral edema. Clin Med Res. 2009 Jun;7(1-2):21-31. doi: 10.3121/cmr.2009.819. Epub 2009 Feb 26.
PubMed 19251582Fazzini B, Markl T, Costas C, Blobner M, Schaller SJ, Prowle J, Puthucheary Z, Wackerhage H. The rate and assessment of muscle wasting during critical illness: a systematic review and meta-analysis. Crit Care. 2023 Jan 3;27(1):2. doi: 10.1186/s13054-022-04253-0.
PubMed 36597123
Study at a glance
From the registry record, last updated by the sponsor on 8 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- An Investigation of The Relationship Between Muscle Mass, Physiological Parameters, and Blood Gas Levels in Adult Patients Hospitalized in The Intensive Care Unit
- ClinicalTrials.gov ID
- NCT07866625
- Acronym / sponsor ID
- AYBU-FTR-BA-12
- Conditions
- Intensive Care (ICU)
- Keywords
- Intensive Care, Muscle Mass, Anthropometric measurements, arterial kan gaze, Oxygen Saturation
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 80 participants (estimated)
- Lead sponsor
- Ankara Yildirim Beyazıt UniversityUniversity, hospital or other
- Study start
- 10 Dec 2025 (actual)
- Primary completion
- 10 Dec 2026 (estimated)
- Study completion
- 10 Dec 2026 (estimated)
- First posted
- 8 Oct 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study was designed to investigate the relationship between muscle mass and physiological parameters and blood gas values in adult patients admitted to the intensive care unit. While muscle mass will be determined using anthropometric measurements, SpO₂, pulse rate, blood pressure, diuresis, and arterial blood gas values will be evaluated. The primary hypothesis of the study is that there is a significant relationship between muscle mass and, in particular, oxygenation and other physiological and blood gas parameters.
Detailed description
Intensive care units are facilities where patients whose physiological balance has been disrupted due to life-threatening illnesses are monitored and treated. In these patients, critical illness disrupts homeostasis, affecting multiple organ functions; sepsis, prolonged mechanical ventilation, and immobilization are significant risk factors for ICU-acquired weakness . These conditions lead to a loss of muscle mass, which negatively affects metabolic reserve, respiratory muscle strength, and recovery capacity; prolongs the length of hospital stay; and increases the risk of mortality.
Muscle tissue not only enables movement but also plays a critical role in metabolic and systemic regulation through the secretion of myokines. Therefore, muscle loss is not limited to physical weakness but also affects metabolic and systemic functions .Muscle weakness is common in intensive care patients, and losses exceeding 10%-particularly in the first few weeks-are associated with functional impairments .
A decrease in muscle mass can weaken respiratory muscle strength, leading to reduced oxygen saturation, impaired circulatory function, and decreased organ perfusion; this may manifest as pulse variability, low oxygen saturation, and decreased urine output. In a study of patients intubated due to COVID-19-related pneumonia, it was observed that individuals with high muscle density had higher extubation success rates, lower complication rates, and reduced mortality. Similarly, post-discharge measurement of quadriceps muscle mass using BIA showed a positive correlation with long-term recovery.The relationship between muscle mass and respiratory function was examined using DXA, and significant associations were found between restrictive ventilatory dysfunction and muscle mass . These data indicate that muscle mass indirectly supports oxygenation and hemodynamic stability.
The risk of muscle loss increases with prolonged immobilization, mechanical ventilation, and the use of high doses of sedatives. For this reason, the assessment of muscle mass in intensive care patients is important both for monitoring clinical course and for investigating its relationship with physiological parameters such as SpO₂, blood pressure, pulse, diuresis, and blood gas values.
Following a review of the literature, no study was found that examined the relationship between anthropometric measurements of muscle mass and physiological parameters and blood gas values in adult patients admitted to the intensive care unit. In this context, the study was planned.
Type of Study: Observational Study Study Population: Patients admitted to the palliative care intensive care unit, pulmonary intensive care unit, and cardiovascular intensive care unit at Erzurum City Hospital will be included in the study.
Sample Size: In this study, as the primary analysis, the relationship between muscle mass and SpO₂ will be evaluated using a one-way Pearson correlation; similar studies in the literature have shown a moderate correlation (r ≈ 0.30) (Damanti et al., 2022; Lim et al., 2024).Under these assumptions, a power analysis conducted with a statistical power of (1-β) = 0.80 and a significance level of (α = 0.05) determined that a sample size of approximately 67 patients would be required to test the hypothesis that SpO₂ values increase as muscle mass increases. To account for potential data losses, the sample size was planned to be approximately 80 patients.
The criteria used in similar studies in the literature that examine the relationship between muscle mass, muscle strength, and clinical outcomes in intensive care patients will serve as the basis.
Collection of research data: The research data will include adult patients hospitalized in the palliative care, pulmonary, and cardiovascular surgery intensive care units at Erzurum City Hospital. Informed consent forms will be obtained from the patients or their first-degree relatives, as well as from the attending physician in the intensive care unit.
Edema Assessment: This is a routine measurement. It poses no risk to human health. Before measurements begin, patients' upper and lower extremities will be assessed for edema. The assessment will be based on the pitting edema test-performed by applying light pressure with the thumb for 2-3 seconds-and clinical observation. For edema assessment, measurements will be taken at the widest point on the medial surface of the calf, the anterior aspect of the thigh, the midpoint of the femur (midpoint of the SIAS and the patella), the anterior surface of the midpoint of the humerus (between the acromion and the olecranon), and the posterior surface of the midpoint of the humerus (between the acromion and the olecranon).
For grading: 0+: No indentation → No edema; 1+: Mild indentation, recovers quickly → Mild edema, 2+: Moderate indentation, persists for a few seconds → Moderate edema, 3+: Deep indentation, persists for up to 15 seconds → Severe edema, 4+: Very deep indentation, persists for >30 seconds → Very severe edema; these values will be used.
Anthropometric Measurements Patients' circumference measurements and skinfold measurements will be taken while they are lying on their backs. Muscles will be kept relaxed, and a non-elastic anthropometric tape and a Baseline brand skinfold caliper will be used. Measurements will be taken on the right side of the body whenever possible; if access is obstructed, the left or opposite side will be used, and this will be noted on the record form. All measurements will be taken in a single attempt and recorded with a precision of 0.1 mm. The researchers performing the measurements have received training in accordance with the ISAK protocol.
Circumference Measurements: Measurements will be taken at the calf, thigh, and biceps. For the calf, measurements will be taken at the widest point of the calf ; for the thigh, at the midpoint of the femur on the anterior aspect of the thigh and 10 cm above the patella; and for the biceps, from the midpoint of the humerus , and the results will be recorded in centimeters.
Skinfold Measurements: Measurements will be taken from the biceps, triceps, suprailiac region, abdomen, thigh, and calf. Biceps: measured vertically from the midpoint of the humerus; triceps: measured vertically from the midpoint between the acromion and the olecranon; suprailiac: measured obliquely just above the iliac crest; abdomen: measured vertically 2 cm to the right of the navel; thigh: measured vertically from the midpoint of the femur; calf: vertically from the widest point of the calf, and the measurements will be recorded in centimeters.
Measurements will not be taken from the subscapular region, as it is believed this would interfere with patient positioning.
Muscle Mass Calculation: The thigh cross-sectional area formula will be used to calculate muscle mass.
The muscle radius (r) will be determined using the formula: thigh circumference / 2.
Then, using π = 3.14, the formula for muscle cross-sectional area = π (r - (skinfold thickness / 2))² will be used.
Physiological Parameters and Blood Gases: On the day anthropometric measurements are taken, patients' SpO₂, pulse rate, blood pressure, and diuresis will be recorded.
In addition, arterial blood gas (ABG) values will be based on data obtained during routine clinical follow-up within ±12 hours of the measurement time; no additional blood samples will be drawn. Parameters to be recorded: pH, PaO₂, PaCO₂, SaO₂, HCO₃-, base excess (BE), lactate, as well as FiO₂ and ventilator parameters.
Measurement of diuresis: For patients with a urinary catheter: The urine volume collected in the urine bag over a 12-hour period or ±12 hours will be recorded. For patients without a urinary catheter: Urine output by the patient over a 12-hour period (using a soft catheter or urine bag) will be recorded. Unit: To be recorded as mL/12 hours.
All data will be used to evaluate the relationship between muscle mass and oxygen saturation, blood pressure, pulse, diuresis, and blood gas parameters in intensive care patients.
Statistical Analysis: The data obtained from this study will be analyzed using SPSS (The Statistical Package for the Social Sciences). The Shapiro-Wilk test will be used to determine whether the data are normally distributed. The Pearson test will be used for groups with a normal distribution, and the Spearman test will be used for groups without a normal distribution. Results will be evaluated at a significance level of 0.05.
.
Study design
- Observational model
- Other
- Time perspective
- Cross-sectional
- Target follow-up
- 1 Day
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| patients in intensive care | – | –patients in intensive care |
Who may qualify
- Ages
- 18 hours and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- The study data will include adult patients hospitalized in the palliative care intensive care unit, the pulmonary intensive care unit, and the cardiovascular surgery intensive care unit at Erzurum City Hospital.
Key inclusion criteria (1 listed)
- Age: Adult patients aged 18 years and older Clinical unit: Patients admitted to palliative care, pulmonary intensive care, or cardiovascular intensive care units Length of stay: Patients expected to remain in the intensive care unit for at least 48 hours Physical eligibility: Patients with no conditions preventing the measurement of muscle mass Clinical stability: Patients without severe hemodynamic instability or active bleeding at the time of measurement Ethical compliance: Individuals who have volunteered to participate in the study and whose informed consent has been obtained from them or their legal representative
Key exclusion criteria (6 listed)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
muscle mass
Time frame: 10.12.2026
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 8 Oct 2026.
- Background: PubMed 34465493Damanti S, Cristel G, Ramirez GA, Bozzolo EP, Da Prat V, Gobbi A, Centurioni C, Di Gaeta E, Del Prete A, Calabro MG, Calvi MR, Borghi G, Zangrillo A, De Cobelli F, Landoni G, Tresoldi M. Influence of reduced muscle mass and quality on ventilator weaning and complications during intensive care unit stay in COVID-19 patients. Clin Nutr. 2022 Dec;41(12):2965-2972. doi: 10.1016/j.clnu.2021.08.004. Epub 2021 Aug 16.
- Background: PubMed 19251582Brodovicz KG, McNaughton K, Uemura N, Meininger G, Girman CJ, Yale SH. Reliability and feasibility of methods to quantitatively assess peripheral edema. Clin Med Res. 2009 Jun;7(1-2):21-31. doi: 10.3121/cmr.2009.819. Epub 2009 Feb 26.
- Background: PubMed 36597123Fazzini B, Markl T, Costas C, Blobner M, Schaller SJ, Prowle J, Puthucheary Z, Wackerhage H. The rate and assessment of muscle wasting during critical illness: a systematic review and meta-analysis. Crit Care. 2023 Jan 3;27(1):2. doi: 10.1186/s13054-022-04253-0.
- Individual participant dataSharing planned: Yes. all patient data
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Bihter AKINOĞLU principal investigator
Ankara Yildiirm Beyazit University
Sümeyye Karabacak study chair
Erzurum City Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Intensive Care (ICU), run by Ankara Yildirim Beyazıt University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 8 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Bihter Akınoğlu (+905059384136, RGKARDELEN@yahoo.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
muscle mass (time frame: 10.12.2026). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07866625, which also lists 3 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Oct 2026; AzTrials last refreshed its copy on 26 Oct 2026.