Diabetes Mellitus, Type 2PharmaMDNCT03377127
Impact of Pharmacy Clinic on Diabetes Management
A study testing Pharmacy Managed Diabetes Clinic (PMDC) in people with Diabetes Mellitus, Type 2, run by Corewell Health East at 4 sites in United States.
Trial summary
The Beaumont Hospital Royal Oak Outpatient Clinic (and other listed Beaumont recruiting locations) care for over 900 patients with diabetes. In an effort to improve the care provided to our patients, a pharmacist managed diabetes clinic (PMDC) was created. Read more about this study
- Who is it for?
- Ages 18 to 75 years
- Conditions the study is for
- Diabetes Mellitus, Type 2
- What is being tested?
- Pharmacy Managed Diabetes Clinic (PMDC)
- Type of treatment
- Vaccines, Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 86 participants
- Where
- 4 sitesUnited States
- Study dates
- 19 Feb 2018to 30 Nov 2020
- Phase
- Interventional
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
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 to 75 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- high risk diabetes mellitus type 2 patients (hemoglobin ≥ 9%)
- not currently enrolled in PMDC.
- established with a primary care resident internal medicine or medicine-pediatrics resident.
- have a diagnosis of diabetes mellitus type 2.
Who cannot join
- Patients will be excluded if they have been seen by the PMDC within the past 3 months.
- under 18 years of age or over 75 years of age.
- documented as having type 1 diabetes or
- latent autoimmune diabetes of adults.
Trial locations and contacts
4 sites in 1 country.
United States4 sites
Beaumont Geriatric Assessment Center
Berkley, Michigan, 48072
Beaumont Outpatient Clinic
Royal Oak, Michigan, 48073
Beaumont Internal Medicine Center
Southfield, Michigan, 48034
Norton, Klein, Hug, Sabin and Maddens Internal Medicine & Primary Care Practice
Troy, Michigan, 48084
About this study
Official title: PHARM-MD; An Open-Label, Randomized Controlled Phase II Study to Evaluate the Efficacy of a Pharmacist Managed Diabetes Clinic in High-Risk Diabetes Patients
The Beaumont Hospital Royal Oak Outpatient Clinic (and other listed Beaumont recruiting locations) care for over 900 patients with diabetes. In an effort to improve the care provided to our patients, a pharmacist managed diabetes clinic (PMDC) was created. The investigators looked at patients with high-risk diabetes who have received education in the PMDC and compared them to patients that didn't not receive the pharmacy education. Our preliminary data showed a significant decrease in Hemoglobin A1c in the PMDC compared to our standard care cohort. Hemoglobin A1c is a marker of the severity of diabetes mellitus. Based on this data, we designed a randomized controlled trial to better assess the impact of a PMDC on diabetic outcomes.
Read the detailed description
Over the past 20 years, the number of adults with diabetes has tripled in the United States. According to the Centers for Disease Control (CDC), diabetes mellitus (DM) affected 30.2 million American adults in 2015.
Previous studies showed that for each 1% reduction in hemoglobin A1c (HbA1c), there was a corresponding 14% reduction in myocardial infarction, 12% reduction in stroke, and a 37% reduction of microvascular complications.
Based on our preliminary data, a Pharmacist Managed Diabetes Clinic (PMDC) had a decrease in HbA1c of 2.2% in the high-risk diabetes patients from the PMDC cohort versus 0.9% in the standard care cohort (p=0.006). At six months there was a decrease in HbA1c of 3.2% in the PMDC and 1.2% in the standard care cohort (p=0.044).
Our hypothesis is that a pharmacist managed diabetes clinic focused on patient identified diabetes management gaps and goals would have a significant positive impact on diabetes core measures and will result in a higher quality of care at a lower price. A randomized controlled trial (RCT) of our PMDC would provide further clarity on the impact on patient outcomes and important evidence with regard to how the physicians can deliver the best care for this high-risk population.
Trial design This is a randomized open-label, controlled parallel group trial of a pharmacist managed diabetes clinic in high-risk diabetes patients, with a 1:1 allocation to either standard of care (SOC) or SOC and PMDC and a 6-month and 12-month follow-up.
Methods:
The study will be conducted at the listed recruiting sites at Beaumont Hospital. Michigan. The outpatient clinic is a resident clinic that delivers medical care to over 920 patients with diabetes mellitus. The clinic is based on campus at Beaumont Hospital, Royal Oak. Potential subjects with high-risk diabetes mellitus will be identified through weekly reports and from the daily schedule and will be recruited from this pool of patients exclusively.
Intervention The patients will be enrolled over a 6-month period and will be randomly assigned to control group (usual care) and the intervention group (usual care plus PMDC visits). The PMDC is a pharmacist-led clinic that has been functioning in our outpatient clinic since January 2015 and is considered an available resource.
The intervention group patients will be managed by their assigned primary care physicians (PCPs), per standard of care and will have scheduled six extra face-to-face visits with the pharmacists for the 6 month duration of the intervention. The PMDC visits will be scheduled more frequent in the first 2 months of the intervention to ensure patients' engagement and provide enough opportunities and time to address all the patients' goals and concerns. The PMDC visit encounters will focus on patient identified goals for the management of their diabetes. Initial visit in the PMDC will be 60-90 minutes with follow up visits lasting 30-45 minutes. Patients will be asked to describe their own gaps in knowledge and to identify their own management goals. Identification of knowledge gaps will allow targeted patient education to close those gaps. Other educational opportunities will potentially include diabetes mellitus pathophysiology, blood glucose goals, HbA1c goals, management of hyperglycemic and hypoglycemic episodes, review of medications, and counseling regarding diet and exercise. Pharmacists have the discretion to make medication adjustments and initiate new medications pertinent to the management of diabetic comorbidities. The model is a collaborative practice agreement between the pharmacist and the primary care physician.
The control group patients will be managed by their assigned PCPs, per standard of care. Management per standard of care includes referrals to ophthalmology for dilated eye exam, nephrology for nephropathy management, cardiology for macrovascular complications management, neurology for neuropathy or neurologic complications, diabetic education, laboratory studies, and vaccinations and will be ordered or performed at the discretion of each patient's PCP.
Outside the intervention, the participants in both groups will be treated identical. They will participate in the standard of care visits at baseline, at 3 months and at 6 months. These visits (visit 1, 6 and 9 in the intervention group and visit 1, 2 and 3 in the standard of care group) will be provided by each patient's primary care physician
- Conditions
- Diabetes Mellitus, Type 2
- Being tested
- Pharmacy Managed Diabetes Clinic (PMDC), Standard of Care (SOC)
- Keywords
- diabetes, pharmacy clinic, education, diabetes complications, hemoglobin A1c, health-care cost, 'no show' rate, compliance, diabetes core measures
- Medical subject headings
- Diabetes Mellitus, Type 2, Diabetes Mellitus, Diabetes Complications, Patient Compliance
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Pharmacy Managed Diabetes Clinic (PMDC)Behavioural
The PMDC visit encounters will focus on patient identified goals for the management of their diabetes. Initial visit in the PMDC will be 60-90 minutes with follow up visits lasting 30-45 minutes.
Standard of Care (SOC)Other
Standard of care will be delivered at the physician discretion per the current American Diabetes Association recommendations
| Study group | Role | What they receive |
|---|---|---|
| Standard of Care (SOC) | Active comparator | The control group patients will be managed by their assigned PCPs, per Standard of Care (SOC), per American Diabetes Association Guidelines. Management per standard of care includes referrals to ophthalmology for dilated eye exam, nephrology for nephropathy management, cardiology for macrovascular complications management, neurology for neuropathy or neurologic complications, diabetic education, laboratory studies, and vaccinations and will be ordered or performed at the discretion of each patient's PCP Receives: Other: Standard of Care (SOC) |
| SOC and PMDC | Experimental | The intervention group patients will be managed by their assigned primary care physicians (PCPs), per American Diabetes Association Guidelines for Standard of Care (SOC) and will have scheduled six extra face-to-face visits with the pharmacists for the 6 month duration of the intervention. The pharmacy managed diabetes clinic (PMDC) visit encounters will focus on patient identified goals for the management of their diabetes. Pharmacists have the discretion to make medication adjustments and initiate new medications pertinent to the management of diabetic comorbidities. The model is a collaborative practice agreement between the pharmacist and the primary care physician. Receives: Behavioral: Pharmacy Managed Diabetes Clinic (PMDC); Other: Standard of Care (SOC) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Hemoglobin A1c at 6 Months
change from baseline in Hemoglobin A1c, measured in % DCCT (Diabetes Control and Complications Trial) units
Measured: 6 months
Hemoglobin A1c at 12 Months
change from baseline in Hemoglobin A1c
Measured: 12 months
Secondary outcomes (19)
Hemoglobin A1c Less Than 8% at 6 Months
Percentage of patients achieving a hemoglobin A1c measurement of less than 8.0%
Measured: 6 months
Hemoglobin A1c Less Than 8% at 12 Months
Percentage of patients achieving a hemoglobin A1c measurement of less than 8.0% DCCT units
Measured: 12 months
Change in Hemoglobin A1c From 6 to 12 Months
The change in hemoglobin A1c (HbA1c), between 6 months and 12 months after randomization.
Measured: 12 months
Achievement of Annual Lipid Panel Testing
percentage of patients complying with annual lipid testing
Measured: 12 months
Statin Compliance
Percentage of patients compliant with statin therapy per the 2013 American College of Cardiology / American Heart Association guidelines.
Measured: 12 months
Blood Pressure
Percentage of patients achieving Blood pressure goal of less than 140/90 at the end of the trial period.
Measured: 12 months
Annual Retinopathy Examination
Percentage of patients compliant with annual retinopathy examination
Measured: 12 months
Annual Nephropathy Examination
Percentage of patients compliant with annual nephropathy examination
Measured: 12 months
Annual Neuropathy Examination
Percentage of patients compliant with annual neuropathy examination
Measured: 12 months
Annual Influenza Vaccine
Percentage of patients compliant with annual influenza vaccine
Measured: 12 months
Annual Pneumonia Vaccine
Percentage of patients compliant with annual pneumonia vaccine
Measured: 12 months
Quality of Life Assessment
Difference between quality of life assessment via the World Health Organization BREF-Quality Of Life at baseline and 12 months.The WHOQOL-BREF consists of 4 domains, Physical Health, Psychological, Social Relationships, and Environment. Each domain is comprised of multiple questions that are considered together in the derivation of each domain score. In addition to the 4 domains, the WHOQOL-BREF includes two stand-alone questions to assess rated QOL and Satisfaction with Health questionnaire administered at baseline and at the conclusion of the trial period. Domain scores are scaled in a positive direction (i.e. higher scores denote higher quality of life) and range from a minimum of 4 to a maximum of 20. The mean score of items within each domain is used to calculate the domain score.A Likert scale from 1-7 was used. (1 - not affected, 7- extremely affected) We compared and reported the mean difference in between 6 months data and baseline data.
Measured: 12 months
Diabetes Related EC Visits at 6 Months
Number of Emergency Center (EC) visits related to hyperglycemia or hypoglycemia
Measured: 6 months
Diabetes Related EC Visits at 12 Months
Number of Emergency Center (EC) visits related to hyperglycemia or hypoglycemia
Measured: 12 months
Total EC Visits at 6 Months
Number of Emergency Center (EC) visits
Measured: 6 months
Total EC Visits at 12 Months
Number of Emergency Center (EC) visits
Measured: 12 months
Inpatient Visits
Total number of inpatient visits
Measured: 12 months
Outpatient Visits
total number of outpatient visits
Measured: 12 months
No-show
percentage of visits missed in clinic
Measured: 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted19 Dec 2017
- Study start19 Feb 2018
- Primary completion22 May 2020
- Study completion30 Nov 2020
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Diabetes Mellitus, Type 2Studies 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
- This is a randomized open-label, controlled parallel group trial of a pharmacist managed diabetes clinic in high-risk diabetes patients, with a 1:1 allocation to either standard of care (SOC) or SOC and PMDC and a 6-month and 12-month follow-up.
- Masking
- Double blind
- Who is masked
- Investigator, Outcomes assessor
- Enrolment
- 86 participants (actual)
Sponsor and investigators
- Lead sponsor
- Corewell Health East
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Alexandra Halalau, Corewell Health East
- Investigators
- Alexandra I Halalau, MD, Principal investigator, Director of Internal Medicine Research
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03377127
- Sponsor's protocol ID
- 2017-494
- Acronym
- PharmaMD
- Status last verified
- Jun 2021
- First submitted
- 13 Dec 2017
- Last updated
- 30 Jun 2021
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Halalau A, Sonmez M, Uddin A, Karabon P, Scherzer Z, Keeney S. Efficacy of a pharmacist-managed diabetes clinic in high-risk diabetes patients, a randomized controlled trial - "Pharm-MD" : Impact of clinical pharmacists in diabetes care. BMC Endocr Disord. 2022 Mar 16;22(1):69. doi: 10.1186/s12902-022-00983-y.
PubMed 35296307Halalau A, Shelden D, Keeney S, Hehar J. Pharm-MD; an open-label, randomized controlled, phase II study to evaluate the efficacy of a pharmacist-managed diabetes clinic in high-risk diabetes patients - study protocol for a randomized controlled trial. Trials. 2018 Aug 24;19(1):458. doi: 10.1186/s13063-018-2836-8.
PubMed 30143033
Study at a glance
From the registry record, last updated by the sponsor on 30 Jun 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- PHARM-MD; An Open-Label, Randomized Controlled Phase II Study to Evaluate the Efficacy of a Pharmacist Managed Diabetes Clinic in High-Risk Diabetes Patients
- ClinicalTrials.gov ID
- NCT03377127
- Acronym / sponsor ID
- PharmaMD / 2017-494
- Conditions
- Diabetes Mellitus, Type 2
- Keywords
- diabetes, pharmacy clinic, education, diabetes complications, hemoglobin A1c, health-care cost, 'no show' rate, compliance
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 86 participants (actual)
- Lead sponsor
- Corewell Health EastUniversity, hospital or other
- Study start
- 19 Feb 2018 (actual)
- Primary completion
- 22 May 2020 (actual)
- Study completion
- 30 Nov 2020 (actual)
- First posted
- 19 Dec 2017 (actual)
- Results
- Posted 3 Jun 2021
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The Beaumont Hospital Royal Oak Outpatient Clinic (and other listed Beaumont recruiting locations) care for over 900 patients with diabetes. In an effort to improve the care provided to our patients, a pharmacist managed diabetes clinic (PMDC) was created. The investigators looked at patients with high-risk diabetes who have received education in the PMDC and compared them to patients that didn't not receive the pharmacy education. Our preliminary data showed a significant decrease in Hemoglobin A1c in the PMDC compared to our standard care cohort. Hemoglobin A1c is a marker of the severity of diabetes mellitus. Based on this data, we designed a randomized controlled trial to better assess the impact of a PMDC on diabetic outcomes.
Detailed description
Over the past 20 years, the number of adults with diabetes has tripled in the United States. According to the Centers for Disease Control (CDC), diabetes mellitus (DM) affected 30.2 million American adults in 2015.
Previous studies showed that for each 1% reduction in hemoglobin A1c (HbA1c), there was a corresponding 14% reduction in myocardial infarction, 12% reduction in stroke, and a 37% reduction of microvascular complications.
Based on our preliminary data, a Pharmacist Managed Diabetes Clinic (PMDC) had a decrease in HbA1c of 2.2% in the high-risk diabetes patients from the PMDC cohort versus 0.9% in the standard care cohort (p=0.006). At six months there was a decrease in HbA1c of 3.2% in the PMDC and 1.2% in the standard care cohort (p=0.044).
Our hypothesis is that a pharmacist managed diabetes clinic focused on patient identified diabetes management gaps and goals would have a significant positive impact on diabetes core measures and will result in a higher quality of care at a lower price. A randomized controlled trial (RCT) of our PMDC would provide further clarity on the impact on patient outcomes and important evidence with regard to how the physicians can deliver the best care for this high-risk population.
Trial design This is a randomized open-label, controlled parallel group trial of a pharmacist managed diabetes clinic in high-risk diabetes patients, with a 1:1 allocation to either standard of care (SOC) or SOC and PMDC and a 6-month and 12-month follow-up.
Methods:
The study will be conducted at the listed recruiting sites at Beaumont Hospital. Michigan. The outpatient clinic is a resident clinic that delivers medical care to over 920 patients with diabetes mellitus. The clinic is based on campus at Beaumont Hospital, Royal Oak. Potential subjects with high-risk diabetes mellitus will be identified through weekly reports and from the daily schedule and will be recruited from this pool of patients exclusively.
Intervention The patients will be enrolled over a 6-month period and will be randomly assigned to control group (usual care) and the intervention group (usual care plus PMDC visits). The PMDC is a pharmacist-led clinic that has been functioning in our outpatient clinic since January 2015 and is considered an available resource.
The intervention group patients will be managed by their assigned primary care physicians (PCPs), per standard of care and will have scheduled six extra face-to-face visits with the pharmacists for the 6 month duration of the intervention. The PMDC visits will be scheduled more frequent in the first 2 months of the intervention to ensure patients' engagement and provide enough opportunities and time to address all the patients' goals and concerns. The PMDC visit encounters will focus on patient identified goals for the management of their diabetes. Initial visit in the PMDC will be 60-90 minutes with follow up visits lasting 30-45 minutes. Patients will be asked to describe their own gaps in knowledge and to identify their own management goals. Identification of knowledge gaps will allow targeted patient education to close those gaps. Other educational opportunities will potentially include diabetes mellitus pathophysiology, blood glucose goals, HbA1c goals, management of hyperglycemic and hypoglycemic episodes, review of medications, and counseling regarding diet and exercise. Pharmacists have the discretion to make medication adjustments and initiate new medications pertinent to the management of diabetic comorbidities. The model is a collaborative practice agreement between the pharmacist and the primary care physician.
The control group patients will be managed by their assigned PCPs, per standard of care. Management per standard of care includes referrals to ophthalmology for dilated eye exam, nephrology for nephropathy management, cardiology for macrovascular complications management, neurology for neuropathy or neurologic complications, diabetic education, laboratory studies, and vaccinations and will be ordered or performed at the discretion of each patient's PCP.
Outside the intervention, the participants in both groups will be treated identical. They will participate in the standard of care visits at baseline, at 3 months and at 6 months. These visits (visit 1, 6 and 9 in the intervention group and visit 1, 2 and 3 in the standard of care group) will be provided by each patient's primary care physician
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (investigator, outcomes assessor)
- Number of arms
- 2
- Model description
- This is a randomized open-label, controlled parallel group trial of a pharmacist managed diabetes clinic in high-risk diabetes patients, with a 1:1 allocation to either standard of care (SOC) or SOC and PMDC and a 6-month and 12-month follow-up.
| Arm | Type | Receives |
|---|---|---|
| Standard of Care (SOC) | Active comparator | Other: Standard of Care (SOC)The control group patients will be managed by their assigned PCPs, per Standard of Care (SOC), per American Diabetes Association Guidelines. Management per standard of care includes referrals to ophthalmology for dilated eye exam, nephrology for nephropathy management, cardiology for macrovascular complications management, neurology for neuropathy or neurologic complications, diabetic education, laboratory studies, and vaccinations and will be ordered or performed at the discretion of each patient's PCP |
| SOC and PMDC | Experimental | Behavioral: Pharmacy Managed Diabetes Clinic (PMDC), Other: Standard of Care (SOC)The intervention group patients will be managed by their assigned primary care physicians (PCPs), per American Diabetes Association Guidelines for Standard of Care (SOC) and will have scheduled six extra face-to-face visits with the pharmacists for the 6 month duration of the intervention. The pharmacy managed diabetes clinic (PMDC) visit encounters will focus on patient identified goals for the management of their diabetes. Pharmacists have the discretion to make medication adjustments and initiate new medications pertinent to the management of diabetic comorbidities. The model is a collaborative practice agreement between the pharmacist and the primary care physician. |
Who may qualify
- Ages
- 18 to 75 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- high risk diabetes mellitus type 2 patients (hemoglobin ≥ 9%)
- not currently enrolled in PMDC.
- established with a primary care resident internal medicine or medicine-pediatrics resident.
- have a diagnosis of diabetes mellitus type 2.
Key exclusion criteria (4 listed)
- Patients will be excluded if they have been seen by the PMDC within the past 3 months.
- under 18 years of age or over 75 years of age.
- documented as having type 1 diabetes or
- latent autoimmune diabetes of adults.
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 |
|---|---|---|
| Pharmacy Managed Diabetes Clinic (PMDC)The PMDC visit encounters will focus on patient identified goals for the management of their diabetes. Initial visit in the PMDC will be 60-90 minutes with follow up visits lasting 30-45 minutes. | Behavioural | SOC and PMDC |
| Standard of Care (SOC)Standard of care will be delivered at the physician discretion per the current American Diabetes Association recommendations | Other | SOC and PMDC, Standard of Care (SOC) |
Primary outcome
Hemoglobin A1c at 6 Months
Time frame: 6 months
change from baseline in Hemoglobin A1c, measured in % DCCT (Diabetes Control and Complications Trial) units
Hemoglobin A1c at 12 Months
Time frame: 12 months
change from baseline in Hemoglobin A1c
19 secondary outcomes
Hemoglobin A1c Less Than 8% at 6 Months
Time frame: 6 months
Hemoglobin A1c Less Than 8% at 12 Months
Time frame: 12 months
Change in Hemoglobin A1c From 6 to 12 Months
Time frame: 12 months
Achievement of Annual Lipid Panel Testing
Time frame: 12 months
Statin Compliance
Time frame: 12 months
Blood Pressure
Time frame: 12 months
Annual Retinopathy Examination
Time frame: 12 months
Annual Nephropathy Examination
Time frame: 12 months
Annual Neuropathy Examination
Time frame: 12 months
Annual Influenza Vaccine
Time frame: 12 months
Annual Pneumonia Vaccine
Time frame: 12 months
Quality of Life Assessment
Time frame: 12 months
Diabetes Related EC Visits at 6 Months
Time frame: 6 months
Diabetes Related EC Visits at 12 Months
Time frame: 12 months
Total EC Visits at 6 Months
Time frame: 6 months
Total EC Visits at 12 Months
Time frame: 12 months
Inpatient Visits
Time frame: 12 months
Outpatient Visits
Time frame: 12 months
No-show
Time frame: 12 months
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Jun 2021.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 35296307Halalau A, Sonmez M, Uddin A, Karabon P, Scherzer Z, Keeney S. Efficacy of a pharmacist-managed diabetes clinic in high-risk diabetes patients, a randomized controlled trial - "Pharm-MD" : Impact of clinical pharmacists in diabetes care. BMC Endocr Disord. 2022 Mar 16;22(1):69. doi: 10.1186/s12902-022-00983-y.
- Derived from this study: PubMed 30143033Halalau A, Shelden D, Keeney S, Hehar J. Pharm-MD; an open-label, randomized controlled, phase II study to evaluate the efficacy of a pharmacist-managed diabetes clinic in high-risk diabetes patients - study protocol for a randomized controlled trial. Trials. 2018 Aug 24;19(1):458. doi: 10.1186/s13063-018-2836-8.
- 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. This study is not recruiting at the moment.
Alexandra I Halalau, MD principal investigator
Director of Internal Medicine Research
4 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Pharmacy Managed Diabetes Clinic (PMDC) in people with Diabetes Mellitus, Type 2, run by Corewell Health East at 4 sites in United States.
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 4 inclusion and 4 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 30 Jun 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 4 sites in United States. 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?
Yes. Results are posted in the registry (first posted 3 Jun 2021). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
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?
Hemoglobin A1c at 6 Months (time frame: 6 months). 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?
On the ClinicalTrials.gov record for NCT03377127, 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 30 Jun 2021.