Pentoxifylline for Treatment of Resistant Major Depression
Primary Purpose
Resistant Major Depression
Status
Completed
Phase
Phase 1
Locations
Iraq
Study Type
Interventional
Intervention
Pentoxifylline
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Resistant Major Depression focused on measuring Bipolar Depression, Pentoxifylline, Resistant Major Depression
Eligibility Criteria
Inclusion Criteria:
- Provide written, voluntary informed consent prior to study enrollment.
- Male or female between the ages of 18 to 65.
- Meets the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-IV) criteria for bipolar I or II, currently experiencing a major depressive episode. A Mini-International Neuropsychiatric Interview (MINI) conducted by physician was used to confirm the diagnosis.
- Meets the criteria for treatment resistant depression (TRD) defined by failure to respond to of at least two treatment trials (antidepressant regimen or electroconvulsive therapy) during the current depressive episode.
- Prior to taking part in the trial, all patients were requested to be antidepressant free for 4 weeks or to be on a fixed psychotropic therapeutic regimen for at least 4 weeks.
Exclusion Criteria:
- Current psychotic symptoms or perceptual problems.
- The presence of a contraindication to PTX, such as a drug allergy or xanthine derivative allergy.
- Patients with substance dependence or abuse.
- Patients with concurrent active medical condition (congestive heart failure, abnormal electrocardiogram, malignancy, schizophrenia, neurological disease).
- Patients with inflammatory disorders and/or auto-immune conditions (rheumatoid arthritis, inflammatory bowel disease, multiple sclerosis, lupus)
Sites / Locations
- Hawler Psychiatric Hospital and Private Clinic
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Pentoxifylline
Control group
Arm Description
Pentoxifylline (tablet): 400 mg twice a day for 12 weeks
Placebo (tablet): twice a day for 12 weeks
Outcomes
Primary Outcome Measures
Hamilton Depression Rating Scale-17 (HAM-D-17) Scores
The HAM-D-17 is a 17-item scale that asks participants to rate the severity of their depression symptoms. Scoring is based on the 17-item scale. The total score ranges from 0 to 52, with higher numbers demonstrating more severe symptoms. Normal scores range from 0 to 7, mild depression ranges from 8 to 16, moderate depression ranges from 17 to 23, and scores of 24 and greater indicate severe depression. Remission is defined as HAM-D-17 total score ≤ 7 (primary outcome).
Secondary Outcome Measures
Response Rate
The number of patients with a ≥ 50% drop in the Hamilton Depression Rating Scale-17 (HAM-D-17) total score.
Remission Rate
The number of patients reaching depression remission. Remission is defined as Hamilton Depression Rating Scale-17 (HAM-D-17) total score ≤ 7.
Serum level of CRP
Peripheral blood samples will be collected to assess changes in the serum levels of C- reactive protein (mg/dl).
Serum level of TNF-α
Peripheral blood samples will be collected to assess changes in the serum levels of tumor necrosis factor alpha (pg/ml).
Serum level of IL-6
Peripheral blood samples will be collected to assess changes in the serum levels of Interleukin-6 (pg/ml).
Full Information
NCT ID
NCT05324735
First Posted
March 25, 2022
Last Updated
September 5, 2022
Sponsor
Hawler Medical University
1. Study Identification
Unique Protocol Identification Number
NCT05324735
Brief Title
Pentoxifylline for Treatment of Resistant Major Depression
Official Title
Pentoxifylline for Treatment of Resistant Major Depression: A Randomized, Double Blind, Placebo Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
September 2022
Overall Recruitment Status
Completed
Study Start Date
December 15, 2021 (Actual)
Primary Completion Date
May 4, 2022 (Actual)
Study Completion Date
June 4, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hawler Medical University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
A growing body of evidence has highlighted the role of inflammation and phosphodiesterases (PDE)-related pathways in the pathogenesis of neuropsychiatric illnesses such as depression/mood disorders. Herein, we aimed to evaluate the therapeutic benefits of pentoxifylline (PTX) in the treatment of therapy-resistant depression (TRD) in adult patients with bipolar depression.
Detailed Description
Depression, which affects an estimated 300 million people worldwide, is the main cause of mental health-related illness burden. Depression keeps people from attaining their full potential, depletes human capital, and is linked to suicide and other forms of mortality. Despite the fact that depressive disorders have a better prognosis than primary psychotic illnesses like schizophrenia, 20%-40% of patients treated with antidepressants do not respond to their initial treatment regimens, and up to 15% do not respond to multiple antidepressant regimens and modalities, such as electroconvulsive shock (ECT) therapy. Since the treatment resistance has been shown to increase the likelihood of full symptomatic recurrence, worsen the treatment course and quality of life; therefore, there is a critical need for innovative treatment techniques for patients who have failed to respond to traditional treatments. Inflammation is one factor that has gotten a lot of attention lately as an etiologic mechanism of treatment-resistant depression (TRD). Increased levels of (pro) inflammatory markers such as tumor necrosis factor-alpha (TNF-α), interleukin (IL)-1, and IL-6 are reported in a considerable percentage of patients with major depressive disorders with or without other comorbidities, including bipolar depression and TRD patients. Also, clinical factors connected to antidepressant response are linked to the reduction of inflammatory cytokines.
Moreover, cytokine antagonists, such as the chimeric anti-TNF-alpha antibody infliximab, has shown antidepressant efficacy. Hence, given the elevated levels of inflammatory activity in TRD patients, new treatments with anti-inflammatory effect might be an effective approach to treat these patients. Pentoxifylline (PTX) is a methylated xanthine derivative that has been used to treat peripheral vascular disease for more than two decades. PTX has anti-inflammatory and phosphodiesterase (PDE) inhibitory effects that enables it to inhibit PDEs competitively. Subsequently, it can increase cAMP levels, activate protein kinase A (PKA), inhibit ILs and TNF-α production, and reduce inflammation. Therefore, PTX-decreased inflammatory activity, may give rapid symptomatic alleviation for medically healthy individuals with TRD depression.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Resistant Major Depression
Keywords
Bipolar Depression, Pentoxifylline, Resistant Major Depression
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Pentoxifylline
Arm Type
Experimental
Arm Description
Pentoxifylline (tablet): 400 mg twice a day for 12 weeks
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
Placebo (tablet): twice a day for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Pentoxifylline
Other Intervention Name(s)
Trental
Intervention Description
All participants will receive pentoxifylline 400 mg (orally ingested) twice a day for 12 weeks.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Sugar Pills
Intervention Description
All participants will receive placebo (orally ingested) twice a day for 12 weeks.
Primary Outcome Measure Information:
Title
Hamilton Depression Rating Scale-17 (HAM-D-17) Scores
Description
The HAM-D-17 is a 17-item scale that asks participants to rate the severity of their depression symptoms. Scoring is based on the 17-item scale. The total score ranges from 0 to 52, with higher numbers demonstrating more severe symptoms. Normal scores range from 0 to 7, mild depression ranges from 8 to 16, moderate depression ranges from 17 to 23, and scores of 24 and greater indicate severe depression. Remission is defined as HAM-D-17 total score ≤ 7 (primary outcome).
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Response Rate
Description
The number of patients with a ≥ 50% drop in the Hamilton Depression Rating Scale-17 (HAM-D-17) total score.
Time Frame
12 weeks
Title
Remission Rate
Description
The number of patients reaching depression remission. Remission is defined as Hamilton Depression Rating Scale-17 (HAM-D-17) total score ≤ 7.
Time Frame
12 weeks
Title
Serum level of CRP
Description
Peripheral blood samples will be collected to assess changes in the serum levels of C- reactive protein (mg/dl).
Time Frame
12 weeks
Title
Serum level of TNF-α
Description
Peripheral blood samples will be collected to assess changes in the serum levels of tumor necrosis factor alpha (pg/ml).
Time Frame
12 weeks
Title
Serum level of IL-6
Description
Peripheral blood samples will be collected to assess changes in the serum levels of Interleukin-6 (pg/ml).
Time Frame
12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Provide written, voluntary informed consent prior to study enrollment.
Male or female between the ages of 18 to 65.
Meets the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-IV) criteria for bipolar I or II, currently experiencing a major depressive episode. A Mini-International Neuropsychiatric Interview (MINI) conducted by physician was used to confirm the diagnosis.
Meets the criteria for treatment resistant depression (TRD) defined by failure to respond to of at least two treatment trials (antidepressant regimen or electroconvulsive therapy) during the current depressive episode.
Prior to taking part in the trial, all patients were requested to be antidepressant free for 4 weeks or to be on a fixed psychotropic therapeutic regimen for at least 4 weeks.
Exclusion Criteria:
Current psychotic symptoms or perceptual problems.
The presence of a contraindication to PTX, such as a drug allergy or xanthine derivative allergy.
Patients with substance dependence or abuse.
Patients with concurrent active medical condition (congestive heart failure, abnormal electrocardiogram, malignancy, schizophrenia, neurological disease).
Patients with inflammatory disorders and/or auto-immune conditions (rheumatoid arthritis, inflammatory bowel disease, multiple sclerosis, lupus)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Talar A Merzamohammad, Pharm. D
Organizational Affiliation
Hawler Medical University, College of Pharmacy, Department of Pharmacology and Toxicology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hawler Psychiatric Hospital and Private Clinic
City
Erbil
ZIP/Postal Code
44001
Country
Iraq
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Pentoxifylline for Treatment of Resistant Major Depression
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