Chronic PainNCT03247725
Efficacy of Pain Monitor, a Smartphone App for Chronic Pain
A study testing pain app and Treatment as usual (medical) in people with Chronic Pain, run by Universitat Jaume I at 1 site in Spain.
Trial summary
The present investigation aims at exploring the effect of including a pain app called Pain Monitor for chronic pain patients' daily monitoring. Three conditions will be set: 1. usual treatment (waiting list) 2. usual treatment + app (without alarms) 3. usual treatment + app (with alarms) Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Chronic Pain
- What is being tested?
- pain app and Treatment as usual (medical)
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 150 participants
- Where
- 1 siteSpain
- Study dates
- 1 Sep 2017to 30 Apr 2018
- Phase
- Interventional
- Are there results?
- None posted in the registry
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
- The patient is over 18 years of age
- The patient has a mobile phone with Android operating system
- The patient has the physical ability to use the application
- The patient does not present psychological and / or cognitive alterations or problems with language that make their participation difficult
- The patient voluntarily wants to participate and signs the informed consent
Who cannot join
- The patient is under 18 years
- The patient does not have a mobile phone or has a mobile phone in which Android is not the operating system (the app is currently only available for Android for economic reasons)
- The patient does not have the physical capacity to use the application
- The patient does not have the capacity to participate due to psychological and / or cognitive alterations or problems with language
- The patient does not want to participate
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Pain Monitor: a Randomized Controlled Trial to Test the Efficacy of a Pain App in the Treatment of Chronic Pain
The present investigation aims at exploring the effect of including a pain app called Pain Monitor for chronic pain patients' daily monitoring. Three conditions will be set:
- usual treatment (waiting list)
- usual treatment + app (without alarms)
- usual treatment + app (with alarms)
Read the detailed description
Chronic pain is defined as one that lasts for at least three to six months, provided that this time is greater than the normal healing period of an injury. This pathology has become an important public health problem due to its high prevalence. In particular, it is estimated that it affects 20-30% of the adult population around the world. Medical interventions are the first-line treatment in recent clinical practice guidelines. Unfortunately, the effectiveness of medical interventions is only modest. Treatments significantly reduce pain on average, but the effect tends to be small . In addition, the drugs are not effective for a large percentage of patients.
What these and other research suggest is that focusing only on large sample studies and the use of average change scores calls into question the usefulness of current patient-centered treatments. As noted by Dr. Turk, when data are averaged, various pain syndromes, drugs, surgical procedures, and studies in different countries are often included, which may mask the efficacy results of different treatments with Different samples. Single case methodology could be one of the ways to overcome these limitations. The single case investigation is a type of experimental study that offers experimental control within a single case.
Some studies have already demonstrated the usefulness of these designs in chronic pain. In fact, the benefits of using this methodology as opposed to large sample studies were discussed recently during the 10th Congress of the European Pain Federation. These benefits include the need for a reduced number of participants, the ability to follow clinical evolution in real time and continuously, the amount of data provided, and applicability when using a control group is impractical or unethical.
The investigators conducting the present investigation recently conducted a study at the Pain Unit of the Vall d'Hebron Hospital to explore the effectiveness of current medical treatments. According to previous investigations, the treatment effect was only small (d = 0.32) and only a percentage of the patients (18.1%) had a clinically significant reduction of pain (ie a reduction greater than 30% ).
From these results and the literature reviewed, a single case design could be an alternative method for research in the Pain Unit. However, the implementation of this type of methodology can be very costly due to the continuous evaluation of the evolution of the patient. In this sense, several studies have already shown that mobile applications (app) can effectively control the evolution of a wide range of pathologies in health settings . In fact, a recent controlled clinical study found that ecological records performed with mobile app had greater reliability than paper-and-pencil records.
Rosser and Eccleston conducted a comprehensive review of existing apps for pain and the conclusion was that there was little evidence to support the use of current apps. Specifically, these authors showed that most apps did not specify whether their content was validated, did not include psychological components and none had been applied in a clinical study. In light of these results, Dr. Carlos Suso Ribera and Dr. Ribera Canudas contacted the research team Labpsitec of Jaume I University, who were developing an application for pain called "Pain Monitor". Dr. Carlos Suso Ribera and Dr. Ribera Canudas of the Pain Unit collaborated with Dr. Azucena García Palacios and Dr. Diana Castilla López of the Universitat Jaume I in the final development of the application of pain, Following the guidelines of Rosser and Eccleston.
App content validity and usability was tested in a previous study at the pain unit of the Vall d'Hebron Hospital (Suso-Ribera et al., in preparation). Thus, the study objective is to test if the introduction of this tool in the day-to-day work of the pain unit improves pain management of chronic pain patients. To do this, it is necessary to compare the evolution of patients who follow the usual treatment at the pain unit (without app) with a group of patients who do use the Pain Monitor app. In addition, the present study investigators have created a new utility that allows alarms to be generated by healthcare professionals in the presence of an undesired event, such as an adverse effect of the medication or a lack of response to medical treatment. Before determining that both the use of the app and this new utility (alarms) are beneficial for patient care, it is necessary to perform a clinical trial comparing the 3 conditions mentioned above:
- usual treatment (waiting list)
- usual treatment + app (without alarms)
- usual treatment + app (with alarms) Therefore, this is a clinical trial without drugs. This is not an observational study since the physicians of patients in the app + alarms condition will be asked to react to an alarm (i.e., if the patient has nausea for 3 consecutive days) by calling the patient and changing the treatment telematically, if necessary, so that the patient can collect the prescription at his primary care center.
If the condition app with alarms results in a better treatment of chronic pain patients, participants of the other two conditions will be offered the possibility to use the app with alarms at the end of the study.
The study will be conducted at the Pain Unit of the Vall d'Hebron Hospital. All study procedures have been approved by the ethical committee of the Vall d'Hebron Hospital.
- Conditions
- Chronic Pain
- Being tested
- pain app, Treatment as usual (medical)
- Medical subject headings
- Chronic Pain
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
pain appOther
Pain Monitor app has been developed by a multidisciplinary pain expert panel, including physicians, psychologists, and nurses. Content has been validated in a previous study and usability has been shown to be excellent.
Treatment as usual (medical)Other
Patients will be offered the usual treatment for their pain, which is not changed by study participation
| Study group | Role | What they receive |
|---|---|---|
| Treatment as usual (waiting list) | Active comparator | Patients at this condition will receive the usual medical treatment at the pain unit, but they will not be monitored daily using the app. Receives: Other: Treatment as usual (medical) |
| Treatment as usual + app (without alarm) | Experimental | Participants at this condition will receive the usual medical treatment for their pain but also they will be monitored daily using the Pain Monitor app. Because alarms will not be generated, physicians will not know if an undesired event is occuring despite the app is actually collecting data. Receives: Other: pain app; Other: Treatment as usual (medical) |
| Treatment as usual + app (with alarm) | Experimental | Participants at this condition will receive the usual medical treatment for their pain but also they will be monitored daily using the Pain Monitor app. Alarms will be generated in the face of certain preestablished events. Physicians will be asked to call patients and change/stop treatment if an alarm is received. Receives: Other: pain app; Other: Treatment as usual (medical) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in pain intensity
A numerical rating scale (0-10 range) will be used.
Measured: Dialy during 30 days (app condition) in the app condition (with and without alarm)
Change in side effects
A list of the most frequent side effects of pain medication was created
Measured: Dialy during 30 days (app condition) in the app condition (with and without alarm)
Change in pain intensity
A numerical rating scale (0-10 range) will be used.
Measured: Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Change in side effects
A list of the most frequent side effects of pain medication was created
Measured: Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Secondary outcomes (14)
Change in mood
Questionnaire on mood validated against the Profile of Mood States
Measured: Dialy during 30 days (app condition) in the app condition (with and without alarm)
Change in mood
Questionnaire on mood validated against the Profile of Mood States
Measured: Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Change in rescue medication use
Amount of rescue medication will be assessed
Measured: Dialy during 30 days (app condition) in the app condition (with and without alarm)
Change in rescue medication use
Amount of rescue medication will be assessed
Measured: Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Change in pain interference
Interference of pain with patient's life
Measured: Dialy during 30 days (app condition) in the app condition (with and without alarm)
Change in pain interference
Interference of pain with patient's life
Measured: Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Change in general health
A general health item was validated against the phsyical health scale of the Short Form 12
Measured: Dialy during 30 days (app condition) in the app condition (with and without alarm)
Change in general health
A general health item was validated against the phsyical health scale of the Short Form 12
Measured: Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Change in fear of pain
2 items validated against the Fear Avoidance Beliefs Scale
Measured: Dialy during 30 days (app condition) in the app condition (with and without alarm)
Change in fear of pain
2 items validated against the Fear Avoidance Beliefs Scale
Measured: Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Change in pain acceptance
2 items validated against the Chronic Pain Acceptance Questionnaire
Measured: Dialy during 30 days (app condition) in the app condition (with and without alarm)
Change in pain acceptance
2 items validated against the Chronic Pain Acceptance Questionnaire
Measured: Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Change in pain catastrophizing
3 items validated against the Pain Catastrophizing Scale
Measured: Dialy during 30 days (app condition) in the app condition (with and without alarm)
Change in pain catastrophizing
3 items validated against the Pain Catastrophizing Scale
Measured: Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted14 Aug 2017
- Study start1 Sep 2017
- Primary completion30 Mar 2018
- Study completion30 Apr 2018
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Chronic PainStudies 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
- Parallel groups
- Model description
- Three conditions. Patients will be randomly assigned to one of the three conditions.
- Masking
- None (open label)
- Enrolment
- 150 participants (actual)
Sponsor and investigators
- Lead sponsor
- Universitat Jaume I
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Carlos Suso Ribera, Universitat Jaume I
- Investigators
- Ángela Mesas Idáñez, MD, Principal investigator, Staff Doctor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03247725
- Sponsor's protocol ID
- UJI_PainMonitor
- Status last verified
- May 2018
- First submitted
- 25 Jul 2017
- Last updated
- 17 May 2018
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Only the two principal investigators, Dr. Mesas and Dr. Suso, will be able to access to individual participant data.
Publications
Rosser BA, Eccleston C. Smartphone applications for pain management. J Telemed Telecare. 2011;17(6):308-12. doi: 10.1258/jtt.2011.101102. Epub 2011 Aug 15.
PubMed 21844177Suso-Ribera C, Mesas A, Medel J, Server A, Marquez E, Castilla D, Zaragoza I, Garcia-Palacios A. Improving pain treatment with a smartphone app: study protocol for a randomized controlled trial. Trials. 2018 Feb 27;19(1):145. doi: 10.1186/s13063-018-2539-1.
PubMed 29482614
Study at a glance
From the registry record, last updated by the sponsor on 17 May 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Pain Monitor: a Randomized Controlled Trial to Test the Efficacy of a Pain App in the Treatment of Chronic Pain
- ClinicalTrials.gov ID
- NCT03247725
- Acronym / sponsor ID
- UJI_PainMonitor
- Conditions
- Chronic Pain
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 150 participants (actual)
- Lead sponsor
- Universitat Jaume IUniversity, hospital or other
- Study start
- 1 Sep 2017 (actual)
- Primary completion
- 30 Mar 2018 (actual)
- Study completion
- 30 Apr 2018 (actual)
- First posted
- 14 Aug 2017 (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.
The present investigation aims at exploring the effect of including a pain app called Pain Monitor for chronic pain patients' daily monitoring. Three conditions will be set:
- usual treatment (waiting list)
- usual treatment + app (without alarms)
- usual treatment + app (with alarms)
Detailed description
Chronic pain is defined as one that lasts for at least three to six months, provided that this time is greater than the normal healing period of an injury. This pathology has become an important public health problem due to its high prevalence. In particular, it is estimated that it affects 20-30% of the adult population around the world. Medical interventions are the first-line treatment in recent clinical practice guidelines. Unfortunately, the effectiveness of medical interventions is only modest. Treatments significantly reduce pain on average, but the effect tends to be small . In addition, the drugs are not effective for a large percentage of patients.
What these and other research suggest is that focusing only on large sample studies and the use of average change scores calls into question the usefulness of current patient-centered treatments. As noted by Dr. Turk, when data are averaged, various pain syndromes, drugs, surgical procedures, and studies in different countries are often included, which may mask the efficacy results of different treatments with Different samples. Single case methodology could be one of the ways to overcome these limitations. The single case investigation is a type of experimental study that offers experimental control within a single case.
Some studies have already demonstrated the usefulness of these designs in chronic pain. In fact, the benefits of using this methodology as opposed to large sample studies were discussed recently during the 10th Congress of the European Pain Federation. These benefits include the need for a reduced number of participants, the ability to follow clinical evolution in real time and continuously, the amount of data provided, and applicability when using a control group is impractical or unethical.
The investigators conducting the present investigation recently conducted a study at the Pain Unit of the Vall d'Hebron Hospital to explore the effectiveness of current medical treatments. According to previous investigations, the treatment effect was only small (d = 0.32) and only a percentage of the patients (18.1%) had a clinically significant reduction of pain (ie a reduction greater than 30% ).
From these results and the literature reviewed, a single case design could be an alternative method for research in the Pain Unit. However, the implementation of this type of methodology can be very costly due to the continuous evaluation of the evolution of the patient. In this sense, several studies have already shown that mobile applications (app) can effectively control the evolution of a wide range of pathologies in health settings . In fact, a recent controlled clinical study found that ecological records performed with mobile app had greater reliability than paper-and-pencil records.
Rosser and Eccleston conducted a comprehensive review of existing apps for pain and the conclusion was that there was little evidence to support the use of current apps. Specifically, these authors showed that most apps did not specify whether their content was validated, did not include psychological components and none had been applied in a clinical study. In light of these results, Dr. Carlos Suso Ribera and Dr. Ribera Canudas contacted the research team Labpsitec of Jaume I University, who were developing an application for pain called "Pain Monitor". Dr. Carlos Suso Ribera and Dr. Ribera Canudas of the Pain Unit collaborated with Dr. Azucena García Palacios and Dr. Diana Castilla López of the Universitat Jaume I in the final development of the application of pain, Following the guidelines of Rosser and Eccleston.
App content validity and usability was tested in a previous study at the pain unit of the Vall d'Hebron Hospital (Suso-Ribera et al., in preparation). Thus, the study objective is to test if the introduction of this tool in the day-to-day work of the pain unit improves pain management of chronic pain patients. To do this, it is necessary to compare the evolution of patients who follow the usual treatment at the pain unit (without app) with a group of patients who do use the Pain Monitor app. In addition, the present study investigators have created a new utility that allows alarms to be generated by healthcare professionals in the presence of an undesired event, such as an adverse effect of the medication or a lack of response to medical treatment. Before determining that both the use of the app and this new utility (alarms) are beneficial for patient care, it is necessary to perform a clinical trial comparing the 3 conditions mentioned above:
- usual treatment (waiting list)
- usual treatment + app (without alarms)
- usual treatment + app (with alarms) Therefore, this is a clinical trial without drugs. This is not an observational study since the physicians of patients in the app + alarms condition will be asked to react to an alarm (i.e., if the patient has nausea for 3 consecutive days) by calling the patient and changing the treatment telematically, if necessary, so that the patient can collect the prescription at his primary care center.
If the condition app with alarms results in a better treatment of chronic pain patients, participants of the other two conditions will be offered the possibility to use the app with alarms at the end of the study.
The study will be conducted at the Pain Unit of the Vall d'Hebron Hospital. All study procedures have been approved by the ethical committee of the Vall d'Hebron Hospital.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
- Model description
- Three conditions. Patients will be randomly assigned to one of the three conditions.
| Arm | Type | Receives |
|---|---|---|
| Treatment as usual (waiting list) | Active comparator | Other: Treatment as usual (medical)Patients at this condition will receive the usual medical treatment at the pain unit, but they will not be monitored daily using the app. |
| Treatment as usual + app (without alarm) | Experimental | Other: pain app, Other: Treatment as usual (medical)Participants at this condition will receive the usual medical treatment for their pain but also they will be monitored daily using the Pain Monitor app. Because alarms will not be generated, physicians will not know if an undesired event is occuring despite the app is actually collecting data. |
| Treatment as usual + app (with alarm) | Experimental | Other: pain app, Other: Treatment as usual (medical)Participants at this condition will receive the usual medical treatment for their pain but also they will be monitored daily using the Pain Monitor app. Alarms will be generated in the face of certain preestablished events. Physicians will be asked to call patients and change/stop treatment if an alarm is received. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- The patient is over 18 years of age
- The patient has a mobile phone with Android operating system
- The patient has the physical ability to use the application
- The patient does not present psychological and / or cognitive alterations or problems with language that make their participation difficult
- The patient voluntarily wants to participate and signs the informed consent
Key exclusion criteria (5 listed)
- The patient is under 18 years
- The patient does not have a mobile phone or has a mobile phone in which Android is not the operating system (the app is currently only available for Android for economic reasons)
- The patient does not have the physical capacity to use the application
- The patient does not have the capacity to participate due to psychological and / or cognitive alterations or problems with language
- The patient does not want to participate
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 |
|---|---|---|
| pain appPain Monitor app has been developed by a multidisciplinary pain expert panel, including physicians, psychologists, and nurses. Content has been validated in a previous study and usability has been shown to be excellent. | Other | Treatment as usual + app (with alarm), Treatment as usual + app (without alarm) |
| Treatment as usual (medical)Patients will be offered the usual treatment for their pain, which is not changed by study participation | Other | Treatment as usual (waiting list), Treatment as usual + app (with alarm), Treatment as usual + app (without alarm) |
Primary outcome
Change in pain intensity
Time frame: Dialy during 30 days (app condition) in the app condition (with and without alarm)
A numerical rating scale (0-10 range) will be used.
Change in side effects
Time frame: Dialy during 30 days (app condition) in the app condition (with and without alarm)
A list of the most frequent side effects of pain medication was created
Change in pain intensity
Time frame: Twice (first day of study and 30 days after, at the end of study) in the TAU condition
A numerical rating scale (0-10 range) will be used.
Change in side effects
Time frame: Twice (first day of study and 30 days after, at the end of study) in the TAU condition
A list of the most frequent side effects of pain medication was created
14 secondary outcomes
Change in mood
Time frame: Dialy during 30 days (app condition) in the app condition (with and without alarm)
Change in mood
Time frame: Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Change in rescue medication use
Time frame: Dialy during 30 days (app condition) in the app condition (with and without alarm)
Change in rescue medication use
Time frame: Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Change in pain interference
Time frame: Dialy during 30 days (app condition) in the app condition (with and without alarm)
Change in pain interference
Time frame: Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Change in general health
Time frame: Dialy during 30 days (app condition) in the app condition (with and without alarm)
Change in general health
Time frame: Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Change in fear of pain
Time frame: Dialy during 30 days (app condition) in the app condition (with and without alarm)
Change in fear of pain
Time frame: Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Change in pain acceptance
Time frame: Dialy during 30 days (app condition) in the app condition (with and without alarm)
Change in pain acceptance
Time frame: Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Change in pain catastrophizing
Time frame: Dialy during 30 days (app condition) in the app condition (with and without alarm)
Change in pain catastrophizing
Time frame: Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 May 2018.
- Background: PubMed 21844177Rosser BA, Eccleston C. Smartphone applications for pain management. J Telemed Telecare. 2011;17(6):308-12. doi: 10.1258/jtt.2011.101102. Epub 2011 Aug 15.
- Derived from this study: PubMed 29482614Suso-Ribera C, Mesas A, Medel J, Server A, Marquez E, Castilla D, Zaragoza I, Garcia-Palacios A. Improving pain treatment with a smartphone app: study protocol for a randomized controlled trial. Trials. 2018 Feb 27;19(1):145. doi: 10.1186/s13063-018-2539-1.
- Individual participant dataSharing planned: No. Only the two principal investigators, Dr. Mesas and Dr. Suso, will be able to access to individual participant 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. This study is not recruiting at the moment.
Ángela Mesas Idáñez, MD principal investigator
Staff Doctor
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing pain app and Treatment as usual (medical) in people with Chronic Pain, run by Universitat Jaume I 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 5 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: finished, as of the sponsor's last update on 17 May 2018. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Change in pain intensity (time frame: Dialy during 30 days (app condition) in the app condition (with and without alarm)). The study lists 4 primary outcomes in all. 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 NCT03247725, which also lists 2 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 17 May 2018.