Lung TransplantationI-TRAIN-LTxNCT06963190
Impact of Inspiratory Muscle Training (IMT) With Intermittent Variable Resistance (IVR) Versus Constant Resistance (CR) on Functional Capacity in Lung Transplantation (LTx) Patients (I-TRAIN-LTx Study)
A study testing Constant Resistance (CR) and Intermittent Variable Resistance (IVR) in people with Lung Transplantation, run by Hospital Universitario Marqués de Valdecilla at 1 site in Spain.
Trial summary
Objectives: Primary Objective: To compare Maximum Inspiratory Pressure (MIP) in lung transplant (LT) patients between the use of inspiratory muscle training (IMT) with intermittent variable resistance (IVR) or constant resistance (CR) during the first six months post-transplant. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Lung Transplantation
- What is being tested?
- Constant Resistance (CR) and Intermittent Variable Resistance (IVR)
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 42 participants
- Where
- 1 siteSpain
- Study dates
- 31 Aug 2025to Dec 2027
- Phase
- Interventional
- 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 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Adult patient (≥18 years) who has undergone lung transplantation (single-lung or double-lung) at our center.
- Alert and cooperative (Glasgow Coma Scale >13 points).
- Hemodynamically stable (blood pressure between 90/60 and 165/90 mmHg; heart rate between 60 and 130 beats per minute).
- No disabling dyspnea at rest (maintained at mild levels according to the Borg scale or NYHA class I-II), even if requiring supplemental oxygen with a saturation >89%.
- No limiting chest pain interfering with respiratory therapy.
Who cannot join
- Patients unable to cooperate with treatment due to lack of necessary instrumental cognitive skills.
- Perceived non-adherence to pharmacological and non-pharmacological treatment by healthcare personnel.
- Need for continuous non-invasive mechanical ventilation, high-flow oxygen therapy, or Venturi mask.
- Patients with significant neurological disorders, severe polyneuropathies, or stroke (CVA).
- Presence of tracheostomy, active hemoptysis, bronchial suture dehiscence.
- Significant air leak with clinical repercussions.
- Any clinical condition that, in the investigator's judgment, poses a risk to the patient.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Spain1 site
Hospital Universitario Marqués de Valdecilla
Santander, Cantabria, 39008
About this study
Official title: Impact of Inspiratory Muscle Training (IMT) With Intermittent Variable Resistance (IVR) Versus Constant Resistance (CR) on Functional Capacity in Lung Transplantation (LTx) Patients
- Objectives: Primary Objective: To compare Maximum Inspiratory Pressure (MIP) in lung transplant (LT) patients between the use of inspiratory muscle training (IMT) with intermittent variable resistance (IVR) or constant resistance (CR) during the first six months post-transplant.
Secondary Objectives: To determine whether there are differences in the outcomes of IMT with IVR and IMT with CR in the six-minute walk test, spirometry values, and arterial blood gas analysis within the first six months post-transplant.
Read more
To analyze the influence of relevant clinical conditions on dependent variables in both groups: duration of mechanical ventilation during the immediate postoperative period of LT and presence of diaphragmatic paralysis.
To analyze the proportion of patients with Baseline Lung Allograft Dysfunction (BLAD) in both intervention groups.
- Methodology: Design: Open-label, two-arm, randomized clinical trial.
Intervention: Random allocation into:
CR Group: Will perform IMT at 30% of MIP. IVR Group: Will perform IMT at 30% and 60% of MIP.
Population and Sample: Patients undergoing lung transplantation.
Demographic and LT-related variables: Sex, date of birth, height, weight, body mass index, type of transplant, underlying disease leading to transplantation, phrenic paralysis, length of stay in the intensive care unit, days on mechanical ventilation, primary graft dysfunction, and acute rejection.
Dependent Variables: MIP, spirometry, arterial blood gas analysis, six-minute walk test, and BLAD criteria.
Read the detailed description
Background and Current State of Knowledge
According to the World Health Organization, chronic obstructive pulmonary disease (COPD) is the fourth leading cause of death worldwide, accounting for 3.5 million deaths in 2021, approximately 5% of all global fatalities.
Lung transplantation (LT) is a treatment option for patients with severe, irreversible, non-neoplastic chronic respiratory diseases when all other therapeutic options have been exhausted, provided that post-transplant survival and quality of life are superior to those of the underlying condition.
The International Society for Heart and Lung Transplantation (ISHLT) has recorded over 70,000 lung transplants worldwide since its registry began. In recent years, the number of annual lung transplants has increased significantly.
In Spain, a global leader in organ donation and solid organ transplantation in 2023, 479 lung transplants were performed, according to the Spanish National Transplant Organization (ONT). The main indications for lung transplantation were COPD (40%), diffuse interstitial lung disease (DILD) (36%), and other conditions (24%), including retransplantation, cystic fibrosis, bronchiectasis, and pulmonary hypertension.
Patients with COPD and DILD, the most common indications for lung transplantation, experience exercise intolerance, dyspnea, and decreased respiratory muscle strength and endurance-symptoms that worsen post-transplant. Newly transplanted patients have denervated lungs, a lack of cough reflex, and reduced mucociliary clearance due to factors such as mechanical ventilation, anesthesia, or immunosuppressive medications. These factors may contribute to early complications, including atelectasis and secondary infections, which require treatment through respiratory physiotherapy.
The diaphragm is the primary inspiratory muscle, and diaphragmatic dysfunction can involve partial or total loss of function, affecting one or both hemidiaphragms. Main issues include reduced muscle strength, endurance alterations, limited mobility, and diaphragmatic fatigue.
In COPD patients, diaphragmatic structural changes include negative alterations and adaptive modifications, directly impacting diaphragm function and its ability to meet respiratory demands.
Among the negative changes, diaphragmatic atrophy is prominent, with a 30% reduction in myosin heavy chain content in mild-to-moderate COPD patients and a 30%-40% decrease in muscle fiber cross-sectional area in severe cases. This leads to loss of contractile strength, elasticity, and functionality.
Conversely, adaptive changes occur in response to increased respiratory demand, notably the transformation of type II muscle fibers into type I fibers, which are more fatigue-resistant and have a predominantly oxidative metabolism. However, despite enhancing endurance, these adaptations reduce total diaphragmatic strength, as type I fibers generate less force than type II fibers.
Idiopathic pulmonary fibrosis (IPF), the most common form of DILD, shares similarities with COPD in terms of exercise limitation due to dyspnea. Studies show reduced diaphragmatic mobility during deep breathing and greater muscle weakness in IPF patients compared to healthy individuals.
Although chronic lung allograft dysfunction (CLAD) remains the primary cause of post-transplant mortality, a newly described phenomenon called Baseline Lung Allograft Dysfunction (BLAD) is characterized by an inability to achieve FEV1 and/or FVC values above 80%. Although its causes remain unclear, alterations in MIP may be related.
Several studies on IMT in COPD and IPF patients, as well as post-cardiac surgery patients, conclude that IMT is beneficial in reducing dyspnea, improving muscle strength and endurance, increasing exercise capacity, and enhancing quality of life.
MIP is determined by performing a maximal inspiration from residual volume under static conditions, assessing diaphragm strength. However, no consensus exists on the required load to strengthen the diaphragm. Training loads vary from 30% to 60% of MIP, with most protocols recommending 10-15 minutes twice daily at a constant load.
Few studies have examined IMT in recently transplanted patients. A 2024 review by Polastri et al. analyzed 64 lung transplant candidates and recipients, showing that participants used a threshold valve device with resistance levels between 30% and over 50% of MIP, training twice daily with 30-60 inspirations or for 15 minutes. A 2022 pilot study by Graur et al. found significant improvements in MIP and six-minute walk test results in transplanted patients performing IMT. Training intensity progressively increased from 15% to 60% of MIP within the first month. Most other studies have small sample sizes or focus on lung transplant candidates or heart-lung transplant recipients.
Hypothesis
Primary Hypothesis: IMT with IVR has a greater impact on functional capacity than IMT with CR in lung transplant patients in the short and medium term.
Secondary Hypotheses:
IMT with IVR significantly improves MIP, six-minute walk test results, spirometry values, and arterial blood gas levels compared to IMT with CR in lung transplant patients in the short and medium term.
Patients requiring longer mechanical ventilation durations and those with diaphragmatic paralysis will benefit more from IMT with IVR than IMT with CR.
The proportion of BLAD patients will be lower in the IVR group than in the CR group.
Ethical Considerations The study will be approved by the Ethics Committee for Drug Research (CEIm). Patients will provide written informed consent, adhering to EU Regulation 2016/679 (GDPR) and Spanish Organic Law 3/2018 on data protection. The study follows the Declaration of Helsinki and Good Clinical Practices (GCP) guidelines.
- Conditions
- Lung Transplantation
- Being tested
- Constant Resistance (CR), Intermittent Variable Resistance (IVR)
- Keywords
- Respiratory Muscle Training, Lung Transplantation, Respiratory Function Tests, Spirometry, Blood Gas Analysis, Walk Test, Diaphragm Paralysis
- Medical subject headings
- Respiratory Paralysis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Constant Resistance (CR)Other
Will perform inspiratory muscle training at 30% of MIP. Two daily sessions of 30 breaths or 10 minutes.
Intermittent Variable Resistance (IVR)Other
Will perform inspiratory muscle training at 30% of MIP. This will consist of two daily sessions of 30 breaths or 10 minutes. Additionally, the participant will complete 8 sets of 3 repetitions at 60% of the MIP, distributed throughout the day, with a one-minute rest between each repetition.
| Study group | Role | What they receive |
|---|---|---|
| Constant Resistance (CR) | Active comparator | Not described Receives: Other: Constant Resistance (CR) |
| Intermittent Variable Resistance (IVR) | Experimental | Not described Receives: Other: Intermittent Variable Resistance (IVR) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Dependent variables
Maximal inspiratory pressure: Expressed in cmH₂O.
Measured: Measurements will be performed at the time of recruitment (baseline) and at months 1, 2, 4, and 6 post-transplant.
Dependent variables
Spirometry: Forced expiratory volume in the first second (FEV1) in mL and percentage of predicted, forced vital capacity (FVC) in mL and percentage, and FEV1/FVC ratio.
Measured: Measurements will be performed at the time of recruitment (baseline) and at months 1, 2, 4, and 6 post-transplant.
Secondary outcomes (2)
Demographic and Transplant-Related Variables
Length of stay in the intensive care unit (ICU) (days)
Measured: Measurements will be performed at the time of recruitment (baseline)
Demographic and Transplant-Related Variables
Duration of mechanical ventilation (days)
Measured: Measurements will be performed at the time of recruitment (baseline)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 May 2025
- Study start31 Aug 2025
- Primary completionJun 2027 (estimated)
- Study completionDec 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Lung TransplantationStudies 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Sequential
- Masking
- None (open label)
- Enrolment
- 42 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Hospital Universitario Marqués de Valdecilla
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Andrea Pérez Zabaleta, Hospital Universitario Marqués de Valdecilla
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06963190
- Sponsor's protocol ID
- Impact of IMT en LTX patients
- Acronym
- I-TRAIN-LTx
- Status last verified
- Aug 2025
- First submitted
- 16 Mar 2025
- Last updated
- 8 Sep 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 8 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Impact of Inspiratory Muscle Training (IMT) With Intermittent Variable Resistance (IVR) Versus Constant Resistance (CR) on Functional Capacity in Lung Transplantation (LTx) Patients
- ClinicalTrials.gov ID
- NCT06963190
- Acronym / sponsor ID
- I-TRAIN-LTx / Impact of IMT en LTX patients
- Conditions
- Lung Transplantation
- Keywords
- Respiratory Muscle Training, Lung Transplantation, Respiratory Function Tests, Spirometry, Blood Gas Analysis, Walk Test, Diaphragm Paralysis
- Study type
- Interventional
- Recruitment status
- Enrolling by invitation
- Enrolment
- 42 participants (estimated)
- Lead sponsor
- Hospital Universitario Marqués de ValdecillaUniversity, hospital or other
- Study start
- 31 Aug 2025 (actual)
- Primary completion
- Jun 2027 (estimated)
- Study completion
- Dec 2027 (estimated)
- First posted
- 8 May 2025 (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.
- Objectives: Primary Objective: To compare Maximum Inspiratory Pressure (MIP) in lung transplant (LT) patients between the use of inspiratory muscle training (IMT) with intermittent variable resistance (IVR) or constant resistance (CR) during the first six months post-transplant.
Secondary Objectives: To determine whether there are differences in the outcomes of IMT with IVR and IMT with CR in the six-minute walk test, spirometry values, and arterial blood gas analysis within the first six months post-transplant.
To analyze the influence of relevant clinical conditions on dependent variables in both groups: duration of mechanical ventilation during the immediate postoperative period of LT and presence of diaphragmatic paralysis.
To analyze the proportion of patients with Baseline Lung Allograft Dysfunction (BLAD) in both intervention groups.
- Methodology: Design: Open-label, two-arm, randomized clinical trial.
Intervention: Random allocation into:
CR Group: Will perform IMT at 30% of MIP. IVR Group: Will perform IMT at 30% and 60% of MIP.
Population and Sample: Patients undergoing lung transplantation.
Demographic and LT-related variables: Sex, date of birth, height, weight, body mass index, type of transplant, underlying disease leading to transplantation, phrenic paralysis, length of stay in the intensive care unit, days on mechanical ventilation, primary graft dysfunction, and acute rejection.
Dependent Variables: MIP, spirometry, arterial blood gas analysis, six-minute walk test, and BLAD criteria.
Detailed description
Background and Current State of Knowledge
According to the World Health Organization, chronic obstructive pulmonary disease (COPD) is the fourth leading cause of death worldwide, accounting for 3.5 million deaths in 2021, approximately 5% of all global fatalities.
Lung transplantation (LT) is a treatment option for patients with severe, irreversible, non-neoplastic chronic respiratory diseases when all other therapeutic options have been exhausted, provided that post-transplant survival and quality of life are superior to those of the underlying condition.
The International Society for Heart and Lung Transplantation (ISHLT) has recorded over 70,000 lung transplants worldwide since its registry began. In recent years, the number of annual lung transplants has increased significantly.
In Spain, a global leader in organ donation and solid organ transplantation in 2023, 479 lung transplants were performed, according to the Spanish National Transplant Organization (ONT). The main indications for lung transplantation were COPD (40%), diffuse interstitial lung disease (DILD) (36%), and other conditions (24%), including retransplantation, cystic fibrosis, bronchiectasis, and pulmonary hypertension.
Patients with COPD and DILD, the most common indications for lung transplantation, experience exercise intolerance, dyspnea, and decreased respiratory muscle strength and endurance-symptoms that worsen post-transplant. Newly transplanted patients have denervated lungs, a lack of cough reflex, and reduced mucociliary clearance due to factors such as mechanical ventilation, anesthesia, or immunosuppressive medications. These factors may contribute to early complications, including atelectasis and secondary infections, which require treatment through respiratory physiotherapy.
The diaphragm is the primary inspiratory muscle, and diaphragmatic dysfunction can involve partial or total loss of function, affecting one or both hemidiaphragms. Main issues include reduced muscle strength, endurance alterations, limited mobility, and diaphragmatic fatigue.
In COPD patients, diaphragmatic structural changes include negative alterations and adaptive modifications, directly impacting diaphragm function and its ability to meet respiratory demands.
Among the negative changes, diaphragmatic atrophy is prominent, with a 30% reduction in myosin heavy chain content in mild-to-moderate COPD patients and a 30%-40% decrease in muscle fiber cross-sectional area in severe cases. This leads to loss of contractile strength, elasticity, and functionality.
Conversely, adaptive changes occur in response to increased respiratory demand, notably the transformation of type II muscle fibers into type I fibers, which are more fatigue-resistant and have a predominantly oxidative metabolism. However, despite enhancing endurance, these adaptations reduce total diaphragmatic strength, as type I fibers generate less force than type II fibers.
Idiopathic pulmonary fibrosis (IPF), the most common form of DILD, shares similarities with COPD in terms of exercise limitation due to dyspnea. Studies show reduced diaphragmatic mobility during deep breathing and greater muscle weakness in IPF patients compared to healthy individuals.
Although chronic lung allograft dysfunction (CLAD) remains the primary cause of post-transplant mortality, a newly described phenomenon called Baseline Lung Allograft Dysfunction (BLAD) is characterized by an inability to achieve FEV1 and/or FVC values above 80%. Although its causes remain unclear, alterations in MIP may be related.
Several studies on IMT in COPD and IPF patients, as well as post-cardiac surgery patients, conclude that IMT is beneficial in reducing dyspnea, improving muscle strength and endurance, increasing exercise capacity, and enhancing quality of life.
MIP is determined by performing a maximal inspiration from residual volume under static conditions, assessing diaphragm strength. However, no consensus exists on the required load to strengthen the diaphragm. Training loads vary from 30% to 60% of MIP, with most protocols recommending 10-15 minutes twice daily at a constant load.
Few studies have examined IMT in recently transplanted patients. A 2024 review by Polastri et al. analyzed 64 lung transplant candidates and recipients, showing that participants used a threshold valve device with resistance levels between 30% and over 50% of MIP, training twice daily with 30-60 inspirations or for 15 minutes. A 2022 pilot study by Graur et al. found significant improvements in MIP and six-minute walk test results in transplanted patients performing IMT. Training intensity progressively increased from 15% to 60% of MIP within the first month. Most other studies have small sample sizes or focus on lung transplant candidates or heart-lung transplant recipients.
Hypothesis
Primary Hypothesis: IMT with IVR has a greater impact on functional capacity than IMT with CR in lung transplant patients in the short and medium term.
Secondary Hypotheses:
IMT with IVR significantly improves MIP, six-minute walk test results, spirometry values, and arterial blood gas levels compared to IMT with CR in lung transplant patients in the short and medium term.
Patients requiring longer mechanical ventilation durations and those with diaphragmatic paralysis will benefit more from IMT with IVR than IMT with CR.
The proportion of BLAD patients will be lower in the IVR group than in the CR group.
Ethical Considerations The study will be approved by the Ethics Committee for Drug Research (CEIm). Patients will provide written informed consent, adhering to EU Regulation 2016/679 (GDPR) and Spanish Organic Law 3/2018 on data protection. The study follows the Declaration of Helsinki and Good Clinical Practices (GCP) guidelines.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Sequential
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Constant Resistance (CR) | Active comparator | Other: Constant Resistance (CR) |
| Intermittent Variable Resistance (IVR) | Experimental | Other: Intermittent Variable Resistance (IVR) |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- Adult patient (≥18 years) who has undergone lung transplantation (single-lung or double-lung) at our center.
- Alert and cooperative (Glasgow Coma Scale >13 points).
- Hemodynamically stable (blood pressure between 90/60 and 165/90 mmHg; heart rate between 60 and 130 beats per minute).
- No disabling dyspnea at rest (maintained at mild levels according to the Borg scale or NYHA class I-II), even if requiring supplemental oxygen with a saturation >89%.
- No limiting chest pain interfering with respiratory therapy.
Key exclusion criteria (7 listed)
- Patients unable to cooperate with treatment due to lack of necessary instrumental cognitive skills.
- Perceived non-adherence to pharmacological and non-pharmacological treatment by healthcare personnel.
- Need for continuous non-invasive mechanical ventilation, high-flow oxygen therapy, or Venturi mask.
- Patients with significant neurological disorders, severe polyneuropathies, or stroke (CVA).
- Presence of tracheostomy, active hemoptysis, bronchial suture dehiscence.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Constant Resistance (CR)Will perform inspiratory muscle training at 30% of MIP. Two daily sessions of 30 breaths or 10 minutes. | Other | Constant Resistance (CR) |
| Intermittent Variable Resistance (IVR)Will perform inspiratory muscle training at 30% of MIP. This will consist of two daily sessions of 30 breaths or 10 minutes. Additionally, the participant will complete 8 sets of 3 repetitions at 60% of the MIP, distributed throughout the day, with a one-minute rest between each repetition. | Other | Intermittent Variable Resistance (IVR) |
Primary outcome
Dependent variables
Time frame: Measurements will be performed at the time of recruitment (baseline) and at months 1, 2, 4, and 6 post-transplant.
Maximal inspiratory pressure: Expressed in cmH₂O.
Dependent variables
Time frame: Measurements will be performed at the time of recruitment (baseline) and at months 1, 2, 4, and 6 post-transplant.
Spirometry: Forced expiratory volume in the first second (FEV1) in mL and percentage of predicted, forced vital capacity (FVC) in mL and percentage, and FEV1/FVC ratio.
2 secondary outcomes
Demographic and Transplant-Related Variables
Time frame: Measurements will be performed at the time of recruitment (baseline)
Demographic and Transplant-Related Variables
Time frame: Measurements will be performed at the time of recruitment (baseline)
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 Sep 2025.
- Individual participant dataSharing planned: No
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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.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Constant Resistance (CR) and Intermittent Variable Resistance (IVR) in people with Lung Transplantation, run by Hospital Universitario Marqués de Valdecilla at 1 site in Spain.
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 5 inclusion and 7 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: enrolling by invitation, as of the sponsor's last update on 8 Sep 2025. 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 Spain. 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?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Dependent variables (time frame: Measurements will be performed at the time of recruitment (baseline) and at months 1, 2, 4, and 6 post-transplant.). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 Sep 2025.