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Clinical Trial of Efficacy and Safety of Prospecta in the Treatment of Attention Deficit/Hyperactivity Disorder in Children

Primary Purpose

Attention Deficit Hyperactivity Disorder

Status
Completed
Phase
Phase 3
Locations
Russian Federation
Study Type
Interventional
Intervention
Prospecta
Placebo
Sponsored by
Materia Medica Holding
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Attention Deficit Hyperactivity Disorder focused on measuring in children

Eligibility Criteria

7 Years - 12 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Male and female children aged 7-12 years old inclusive.
  2. Children with verified diagnosis of ADHD.
  3. Presence of all ADHD criteria according to DSM-V (see appendix 1):

A. persistent pattern of inattention and/or hyperactivity-impulsivity that interferes with functioning or development, as characterized by (1) and/or (2):

  1. Attention deficit: Six (or more) of the following symptoms have persisted for at least 6 months to a degree that is inconsistent with developmental level and that negatively impacts directly on social and academic/occupational activities:

    • Often fails to give close attention to details or makes careless mistakes in schoolwork, at work, or during other activities (e.g., overlooks or misses details, work is inaccurate).
    • Often has difficulty sustaining attention in tasks or play activities (e.g., has difficulty remaining focused during lectures, conversations, or lengthy reading).
    • Often does not seem to listen when spoken to directly (e.g., mind seems elsewhere, even in the absence of any obvious distraction).
    • Often does not follow through on instructions and fails to finish schoolwork, chores, or duties in the workplace (e.g., starts tasks but quickly loses focus and is easily sidetracked).
    • Often has difficulty organizing tasks and activities (e.g., difficulty managing sequential tasks; difficulty keeping materials and belongings in order; messy, disorganized work; has poor time management; fails to meet deadlines).
    • Often avoids, dislikes, or is reluctant to engage in tasks that require sustained mental effort (e.g., schoolwork or homework).
    • Often loses things necessary for tasks or activities (e.g., school materials, pencils, books, tools, wallets, keys, eyeglasses).
    • Is often easily distracted by extraneous stimuli.
    • Is often forgetful in daily activities (e.g., doing chores, running errands).
  2. Hyperactivity/impulsivity: Six (or more) of the following symptoms have persisted for at least 6 months to a degree that is inconsistent with developmental level and that negatively impacts directly on social and academic/occupational activities. Note. The symptoms are not solely a manifestation of oppositional behavior, defiance, hostility, or failure to understand tasks or instructions.

    • Often fidgets with or taps hands or feet or squirms in seat.
    • Often leaves seat in situations when remaining seated is expected (e.g., leaves his or her place in the classroom, in the office or other workplace, or in other situations that require remaining in place).
    • Often runs about or climbs in situations where it is inappropriate.
    • Often unable to play or take part in leisure activities quietly.
    • Is often "on the go" acting as if "driven by a motor" (e.g., is unable to be or uncomfortable being still for extended time).
    • Often talks excessively.
    • Often blurts out an answer before a question has been completed (e.g., completes people's sentences; cannot wait for turn in conversation).
    • Often has trouble waiting his/her turn (e.g., while waiting in line).
    • Often interrupts or intrudes on others (e.g., butts into conversations, games, or activities; may start using other people's things without asking or receiving permission).

B. Several inattentive or hyperactive-impulsive symptoms were present before age 12 years.

C. Several inattentive or hyperactive-impulsive symptoms are present in two or more settings, (e.g., at home, school or work; with friends or relatives).

D. There is clear evidence that the symptoms interfere with, or reduce the quality of, social, school, or work functioning.

E. The symptoms do not occur exclusively during the course of schizophrenia or another psychotic disorder and are not better explained by another mental disorder (e.g., mood disorder, anxiety disorder, dissociative disorder, personality disorder, substance intoxication or withdrawal).

4. ADHD-RS-V ≥ 22. 5. Availability of signed information sheet and informed consent form for the parents/adoptive parents for the subject's participation in the clinical trial.

Exclusion Criteria:

  1. History of central nervous system (CNS) diseases including:

    • Inflammatory diseases of the central nervous system (G00-G09).
    • Systemic atrophies primarily affecting the CNS (G10-G13).
    • Extrapyramidal and movement disorders (G20-G26).
    • Other degenerative diseases of the nervous system (G30-G32).
    • Demyelinating diseases of the CNS (G35-G37).
    • Epilepsy (G40-41).
    • Hydrocephalus (G91).
  2. Childhood autism (F84.0), atypical autism • (F84.1).
  3. Mental retardation (F70-79).
  4. Disorders of psychological development (F80-F89).
  5. History of hyperthyroidism (thyrotoxicosis).
  6. History/suspicion of oncology of any location (except for benign neoplasms).
  7. Any other comorbidity which, in the opinion of the investigator, may affect patient participation in the clinical trial.
  8. Patients allergic to/intolerant of any constituent of the medications used in the treatment.
  9. Hereditary lactose intolerance, malabsorption due to lactose intolerance including congenital or acquired lactase (or other disaccharide) deficiency, galactosemia.
  10. Patients whose parents/adoptive parents will not fulfill the requirements during the study or follow the order of administration of the study drug (SD) products, from the Investigator's point of view.
  11. History of treatment noncompliance, mental diseases, alcoholism or drug abuse in parents/adoptive parents which, according to the investigator, will prevent from following the study procedures.
  12. Administration of the products outlined in section "Prohibited concomitant therapy" within 1 month prior to enrollment.
  13. Patients who have participated in other clinical trials in the past 3 months.
  14. The patient's parent/adoptive parent is a study specialist of the center and is directly involved in the study, or is an immediate family member of the Investigator. Spouses, parents, children, or siblings, regardless of whether they are siblings or adopted are considered immediate family members.
  15. The patient's parent/adoptive parent works at Materia Medica Holding, i.e. they are employees of the Company, temporary employees on a contract basis or appointed officials responsible for conduction of the study or their immediate family members.

Sites / Locations

  • Hospital "Russian Railways - Medicine" of the city of Bryansk
  • Regional Clinical Specialized Psychoneurological Hospital # 1/Children's dispensary department
  • Sverdlovsk Regional Clinical Psychiatric Hospital/Pediatric and adolescent medical and diagnostic department
  • LLC "European Medical Center "UMMC-Health"/Children's polyclinic in the main branch
  • Engels Psychiatric Hospital
  • Kazan State Medical University/Department of Neurology, Neurosurgery and Medical Genetics
  • Children's Republican Clinical Hospital/Neurological department for the treatment of patients with CNS lesions with mental disorders
  • Specialized Clinical Psychiatric Hospital # 1/Dispensary department
  • Russian National Research Medical University named after N.I. Pirogov/Department of Neurology, Neurosurgery and Medical Genetics, Faculty of Pediatrics
  • Research and Practical Center of Pediatric Psychoneurology of Moscow City Health Department/Consultative and polyclinic department
  • Moscow Regional Research Clinical Institute named after M.F. Vladimirsky/Neurology Department of Therapy Department
  • Llc "Nizhmedklinika"
  • Privolzhsky Research Medical University/Department of Neurology, Psychiatry and Narcology FDPO
  • Orenburg Regional Clinical Psychiatric Hospital # 1/Children's psychiatric department
  • Perm State Medical University named after academician E.A. Wagner/Department of Neurology
  • LLC "Treatment and rehabilitation research center "PHOENIX"/Day hospital # 1
  • Ryazan State Medical University named after Acad. I.P. Pavlov/Department of Children's Diseases with a course of hospital pediatrics
  • National Medical Research Center for Psychiatry and Neurology named after V.M. Bekhterev
  • Llc "Doctrina"
  • Institute of the Human Brain named after N.P. Bekhtereva
  • LLC "DNA Research Center"
  • Saratov State Medical University named after V.I. Razumovsky/Department of Neurology. named after K.N. Tretyakov
  • City Clinical Hospital # 2 named after V.I. Razumovsky
  • Saratov City Psychoneurological Dispensary
  • Smolensk Regional Clinical Hospital/Children's neurological department
  • Smolensk Regional Clinical Hospital/Pediatric neurological department
  • LLC "Sunterra"
  • Stavropol Regional Clinical Specialized Psychiatric Hospital # 1/Children's department # 17
  • Regional Clinical Psychoneurological Dispensary/Outpatient clinic # 2
  • Children's City Clinical Hospital of Ulyanovsk city
  • Yaroslavl State Medical University/Department of Polyclinic Pediatrics

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Prospecta

Placebo

Arm Description

One tablet per intake 2 times a day (approximately at the same time), outside of meal (between meals or 15 minutes prior to meal or drinking). The tablet should be held in mouth until completely dissolved.

One tablet per intake 2 times a day (approximately at the same time), outside of meal (between meals or 15 minutes prior to meal or drinking). The tablet should be held in mouth until completely dissolved.

Outcomes

Primary Outcome Measures

Percentage of patients with total ADHD-RS-V reduction ≥25%
Attention Deficit Hyperactivity Disorder-Rating Scale-V (ADHD-V). The home version of ADHD-RS-V will be used separately for children (7-10 years old) and teenagers (11-12 years old). Home version will evaluate behaviour and emotional response in the situations in which the child is with his/her parents. ADHD-RS-V will evaluate 18 symptoms presented as brief characteristics of peculiarities in behaviour and emotional response of children in various situations (at home).

Secondary Outcome Measures

Change in total ADHD-RS-V score
Attention Deficit Hyperactivity Disorder-Rating Scale-V (ADHD-V). Versus baseline.
Change in total ADHD-RS-V score (attention deficit subscale)
Attention Deficit Hyperactivity Disorder-Rating Scale-V (ADHD-V). Attention deficit subscale. Versus baseline.
Change in total ADHD-RS-V score (hyperactivity/impulsivity subscale)
Attention Deficit Hyperactivity Disorder-Rating Scale-V (ADHD-V). Hyperactivity/impulsivity subscale. Versus baseline.
CGI-EI efficacy score
Clinical Global Impression Efficacy Index (CGI-EI). Therapeutic and side effect values. CGI-EI is filled out by an investigator. It is necessary to indicate the level of efficacy of the therapy and the grade of safety of the therapy and circle the index values at the intersection of the selected lines.
Occurrence and nature of adverse events (AEs)
Based on medical records. Occurrence, nature, severity, causality and outcome of adverse events (AEs).
Changes in vital signs (pulse rate (heart rate))
Based on medical records. Vital signs will be measured in a medical setting.
Changes in vital signs (respiration rate (breathing rate))
Based on medical records. Vital signs will be measured in a medical setting.
Changes in vital signs (blood pressure)
Based on medical records. Vital signs will be measured in a medical setting.
Percentage of patients with clinically relevant laboratory abnormalities
Laboratory tests include the following parameters (absolute and relative values): hematology, biochemistry and urinalysis. Laboratory tests will be made by central laboratory.

Full Information

First Posted
September 22, 2020
Last Updated
August 17, 2022
Sponsor
Materia Medica Holding
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1. Study Identification

Unique Protocol Identification Number
NCT04569357
Brief Title
Clinical Trial of Efficacy and Safety of Prospecta in the Treatment of Attention Deficit/Hyperactivity Disorder in Children
Official Title
Multicenter Double-blind Placebo-controlled Parallel-group Randomized Clinical Trial of Efficacy and Safety of Prospecta in the Treatment of Attention Deficit/Hyperactivity Disorder in Children
Study Type
Interventional

2. Study Status

Record Verification Date
November 2021
Overall Recruitment Status
Completed
Study Start Date
November 20, 2020 (Actual)
Primary Completion Date
February 18, 2022 (Actual)
Study Completion Date
February 18, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Materia Medica Holding

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Purpose of the study: • evaluate the efficacy and safety of Prospecta in the treatment of attention deficit/hyperactivity disorder in children.
Detailed Description
Design: a multicenter double-blind placebo-controlled parallel-group randomized clinical trial. The study will enroll children of either age from 7 to 12 years old with diagnosis of attention deficit/hyperactivity disorder (ADHD) verified by Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, American Psychiatric Association" [DSM-V]). After signing patient information sheet and informed consent form by the subject's parent/adoptive parent collection of complaints, medical examination of the children, filling Attention Deficit Hyperactivity Disorder-Rating Scale-V [ADHD-RS-V]) scale by the parent/adoptive parent will be performed, concomitant therapy will be recorded and laboratory tests will be carried out. The study will enroll children with total score ADHD-RS-V ≥ 22. If the inclusion criteria were met and there were no exclusion criteria (Day 1), the patient will be randomized to one of the two groups: group 1 will receive Prospecta at 1 tablet twice daily; group 2 will receive Placebo using the study drug dosing regimen. Treatment period will be 8 weeks, the key examination stages (collection of complaints, recording objective examination findings, repeated filling ADHD-RS-V by parent/adoptive parent) will be made at Visit 1 (Day 1), further in 4 weeks (visit 2) and in 8 weeks (visit 3). Each visit to the research center will be made by the subject accompanied by his/her parent/adoptive parent. Two weeks later (visit 1.1, week 2±3 days) after randomization and initiation of the study therapy and between visits 2 and 3 (visits 2.2, week 6±3 days) the investigator will examine the patient's clinical status (during phone calls). Based on complaints, monitoring of the prescribed therapy therapeutic safety will be assessed. At visit 2 (week 4±3 days) and visit 3 (week 8±3 days) the investigator will collect complaints, record objective examination findings, monitor repeated ADHD-RS-V filling by parent/adoptive parent, the prescribed and concomitant therapy, evaluate therapeutic safety and compliance. In addition at Visit 3 the investigator will complete the Clinical Global Impression Efficacy Index [CGI-EI] scale and collect samples for laboratory testing. The study treatments will be completed. The total length of the observation period is 8 weeks. During the study the treatment for underlying conditions will be allowed with the exception of the drugs indicated in the section "Prohibited concomitant therapy".

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Attention Deficit Hyperactivity Disorder
Keywords
in children

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
double-blind placebo-controlled randomized
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
363 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Prospecta
Arm Type
Experimental
Arm Description
One tablet per intake 2 times a day (approximately at the same time), outside of meal (between meals or 15 minutes prior to meal or drinking). The tablet should be held in mouth until completely dissolved.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
One tablet per intake 2 times a day (approximately at the same time), outside of meal (between meals or 15 minutes prior to meal or drinking). The tablet should be held in mouth until completely dissolved.
Intervention Type
Drug
Intervention Name(s)
Prospecta
Other Intervention Name(s)
MMH-MAP
Intervention Description
Oral administration.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Oral administration.
Primary Outcome Measure Information:
Title
Percentage of patients with total ADHD-RS-V reduction ≥25%
Description
Attention Deficit Hyperactivity Disorder-Rating Scale-V (ADHD-V). The home version of ADHD-RS-V will be used separately for children (7-10 years old) and teenagers (11-12 years old). Home version will evaluate behaviour and emotional response in the situations in which the child is with his/her parents. ADHD-RS-V will evaluate 18 symptoms presented as brief characteristics of peculiarities in behaviour and emotional response of children in various situations (at home).
Time Frame
After 8 weeks of treatment
Secondary Outcome Measure Information:
Title
Change in total ADHD-RS-V score
Description
Attention Deficit Hyperactivity Disorder-Rating Scale-V (ADHD-V). Versus baseline.
Time Frame
After 8 weeks of treatment
Title
Change in total ADHD-RS-V score (attention deficit subscale)
Description
Attention Deficit Hyperactivity Disorder-Rating Scale-V (ADHD-V). Attention deficit subscale. Versus baseline.
Time Frame
After 8 weeks of treatment
Title
Change in total ADHD-RS-V score (hyperactivity/impulsivity subscale)
Description
Attention Deficit Hyperactivity Disorder-Rating Scale-V (ADHD-V). Hyperactivity/impulsivity subscale. Versus baseline.
Time Frame
After 8 weeks of treatment
Title
CGI-EI efficacy score
Description
Clinical Global Impression Efficacy Index (CGI-EI). Therapeutic and side effect values. CGI-EI is filled out by an investigator. It is necessary to indicate the level of efficacy of the therapy and the grade of safety of the therapy and circle the index values at the intersection of the selected lines.
Time Frame
After 8 weeks of treatment
Title
Occurrence and nature of adverse events (AEs)
Description
Based on medical records. Occurrence, nature, severity, causality and outcome of adverse events (AEs).
Time Frame
For 8 weeks of the treatment
Title
Changes in vital signs (pulse rate (heart rate))
Description
Based on medical records. Vital signs will be measured in a medical setting.
Time Frame
For 8 weeks of the treatment
Title
Changes in vital signs (respiration rate (breathing rate))
Description
Based on medical records. Vital signs will be measured in a medical setting.
Time Frame
For 8 weeks of the treatment
Title
Changes in vital signs (blood pressure)
Description
Based on medical records. Vital signs will be measured in a medical setting.
Time Frame
For 8 weeks of the treatment
Title
Percentage of patients with clinically relevant laboratory abnormalities
Description
Laboratory tests include the following parameters (absolute and relative values): hematology, biochemistry and urinalysis. Laboratory tests will be made by central laboratory.
Time Frame
For 8 weeks of the treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male and female children aged 7-12 years old inclusive. Children with verified diagnosis of ADHD. Presence of all ADHD criteria according to DSM-V (see appendix 1): A. persistent pattern of inattention and/or hyperactivity-impulsivity that interferes with functioning or development, as characterized by (1) and/or (2): Attention deficit: Six (or more) of the following symptoms have persisted for at least 6 months to a degree that is inconsistent with developmental level and that negatively impacts directly on social and academic/occupational activities: Often fails to give close attention to details or makes careless mistakes in schoolwork, at work, or during other activities (e.g., overlooks or misses details, work is inaccurate). Often has difficulty sustaining attention in tasks or play activities (e.g., has difficulty remaining focused during lectures, conversations, or lengthy reading). Often does not seem to listen when spoken to directly (e.g., mind seems elsewhere, even in the absence of any obvious distraction). Often does not follow through on instructions and fails to finish schoolwork, chores, or duties in the workplace (e.g., starts tasks but quickly loses focus and is easily sidetracked). Often has difficulty organizing tasks and activities (e.g., difficulty managing sequential tasks; difficulty keeping materials and belongings in order; messy, disorganized work; has poor time management; fails to meet deadlines). Often avoids, dislikes, or is reluctant to engage in tasks that require sustained mental effort (e.g., schoolwork or homework). Often loses things necessary for tasks or activities (e.g., school materials, pencils, books, tools, wallets, keys, eyeglasses). Is often easily distracted by extraneous stimuli. Is often forgetful in daily activities (e.g., doing chores, running errands). Hyperactivity/impulsivity: Six (or more) of the following symptoms have persisted for at least 6 months to a degree that is inconsistent with developmental level and that negatively impacts directly on social and academic/occupational activities. Note. The symptoms are not solely a manifestation of oppositional behavior, defiance, hostility, or failure to understand tasks or instructions. Often fidgets with or taps hands or feet or squirms in seat. Often leaves seat in situations when remaining seated is expected (e.g., leaves his or her place in the classroom, in the office or other workplace, or in other situations that require remaining in place). Often runs about or climbs in situations where it is inappropriate. Often unable to play or take part in leisure activities quietly. Is often "on the go" acting as if "driven by a motor" (e.g., is unable to be or uncomfortable being still for extended time). Often talks excessively. Often blurts out an answer before a question has been completed (e.g., completes people's sentences; cannot wait for turn in conversation). Often has trouble waiting his/her turn (e.g., while waiting in line). Often interrupts or intrudes on others (e.g., butts into conversations, games, or activities; may start using other people's things without asking or receiving permission). B. Several inattentive or hyperactive-impulsive symptoms were present before age 12 years. C. Several inattentive or hyperactive-impulsive symptoms are present in two or more settings, (e.g., at home, school or work; with friends or relatives). D. There is clear evidence that the symptoms interfere with, or reduce the quality of, social, school, or work functioning. E. The symptoms do not occur exclusively during the course of schizophrenia or another psychotic disorder and are not better explained by another mental disorder (e.g., mood disorder, anxiety disorder, dissociative disorder, personality disorder, substance intoxication or withdrawal). 4. ADHD-RS-V ≥ 22. 5. Availability of signed information sheet and informed consent form for the parents/adoptive parents for the subject's participation in the clinical trial. Exclusion Criteria: History of central nervous system (CNS) diseases including: Inflammatory diseases of the central nervous system (G00-G09). Systemic atrophies primarily affecting the CNS (G10-G13). Extrapyramidal and movement disorders (G20-G26). Other degenerative diseases of the nervous system (G30-G32). Demyelinating diseases of the CNS (G35-G37). Epilepsy (G40-41). Hydrocephalus (G91). Childhood autism (F84.0), atypical autism • (F84.1). Mental retardation (F70-79). Disorders of psychological development (F80-F89). History of hyperthyroidism (thyrotoxicosis). History/suspicion of oncology of any location (except for benign neoplasms). Any other comorbidity which, in the opinion of the investigator, may affect patient participation in the clinical trial. Patients allergic to/intolerant of any constituent of the medications used in the treatment. Hereditary lactose intolerance, malabsorption due to lactose intolerance including congenital or acquired lactase (or other disaccharide) deficiency, galactosemia. Patients whose parents/adoptive parents will not fulfill the requirements during the study or follow the order of administration of the study drug (SD) products, from the Investigator's point of view. History of treatment noncompliance, mental diseases, alcoholism or drug abuse in parents/adoptive parents which, according to the investigator, will prevent from following the study procedures. Administration of the products outlined in section "Prohibited concomitant therapy" within 1 month prior to enrollment. Patients who have participated in other clinical trials in the past 3 months. The patient's parent/adoptive parent is a study specialist of the center and is directly involved in the study, or is an immediate family member of the Investigator. Spouses, parents, children, or siblings, regardless of whether they are siblings or adopted are considered immediate family members. The patient's parent/adoptive parent works at Materia Medica Holding, i.e. they are employees of the Company, temporary employees on a contract basis or appointed officials responsible for conduction of the study or their immediate family members.
Facility Information:
Facility Name
Hospital "Russian Railways - Medicine" of the city of Bryansk
City
Bryansk
ZIP/Postal Code
241004
Country
Russian Federation
Facility Name
Regional Clinical Specialized Psychoneurological Hospital # 1/Children's dispensary department
City
Chelyabinsk
ZIP/Postal Code
454087
Country
Russian Federation
Facility Name
Sverdlovsk Regional Clinical Psychiatric Hospital/Pediatric and adolescent medical and diagnostic department
City
Ekaterinburg
ZIP/Postal Code
620030
Country
Russian Federation
Facility Name
LLC "European Medical Center "UMMC-Health"/Children's polyclinic in the main branch
City
Ekaterinburg
ZIP/Postal Code
620144
Country
Russian Federation
Facility Name
Engels Psychiatric Hospital
City
Engels
ZIP/Postal Code
413124
Country
Russian Federation
Facility Name
Kazan State Medical University/Department of Neurology, Neurosurgery and Medical Genetics
City
Kazan
ZIP/Postal Code
420012
Country
Russian Federation
Facility Name
Children's Republican Clinical Hospital/Neurological department for the treatment of patients with CNS lesions with mental disorders
City
Kazan
ZIP/Postal Code
420138
Country
Russian Federation
Facility Name
Specialized Clinical Psychiatric Hospital # 1/Dispensary department
City
Krasnodar
ZIP/Postal Code
350007
Country
Russian Federation
Facility Name
Russian National Research Medical University named after N.I. Pirogov/Department of Neurology, Neurosurgery and Medical Genetics, Faculty of Pediatrics
City
Moscow
ZIP/Postal Code
117997
Country
Russian Federation
Facility Name
Research and Practical Center of Pediatric Psychoneurology of Moscow City Health Department/Consultative and polyclinic department
City
Moscow
ZIP/Postal Code
119602
Country
Russian Federation
Facility Name
Moscow Regional Research Clinical Institute named after M.F. Vladimirsky/Neurology Department of Therapy Department
City
Moscow
ZIP/Postal Code
129110
Country
Russian Federation
Facility Name
Llc "Nizhmedklinika"
City
Nizhny Novgorod
ZIP/Postal Code
603159
Country
Russian Federation
Facility Name
Privolzhsky Research Medical University/Department of Neurology, Psychiatry and Narcology FDPO
City
Nizhny Novgorod
ZIP/Postal Code
603950
Country
Russian Federation
Facility Name
Orenburg Regional Clinical Psychiatric Hospital # 1/Children's psychiatric department
City
Orenburg
ZIP/Postal Code
460006
Country
Russian Federation
Facility Name
Perm State Medical University named after academician E.A. Wagner/Department of Neurology
City
Perm
ZIP/Postal Code
614990
Country
Russian Federation
Facility Name
LLC "Treatment and rehabilitation research center "PHOENIX"/Day hospital # 1
City
Rostov-on-Don
ZIP/Postal Code
344000
Country
Russian Federation
Facility Name
Ryazan State Medical University named after Acad. I.P. Pavlov/Department of Children's Diseases with a course of hospital pediatrics
City
Ryazan
ZIP/Postal Code
390026
Country
Russian Federation
Facility Name
National Medical Research Center for Psychiatry and Neurology named after V.M. Bekhterev
City
Saint Petersburg
ZIP/Postal Code
192019
Country
Russian Federation
Facility Name
Llc "Doctrina"
City
Saint Petersburg
ZIP/Postal Code
197341
Country
Russian Federation
Facility Name
Institute of the Human Brain named after N.P. Bekhtereva
City
Saint Petersburg
ZIP/Postal Code
197376
Country
Russian Federation
Facility Name
LLC "DNA Research Center"
City
Saratov
ZIP/Postal Code
410005
Country
Russian Federation
Facility Name
Saratov State Medical University named after V.I. Razumovsky/Department of Neurology. named after K.N. Tretyakov
City
Saratov
ZIP/Postal Code
410012
Country
Russian Federation
Facility Name
City Clinical Hospital # 2 named after V.I. Razumovsky
City
Saratov
ZIP/Postal Code
410028
Country
Russian Federation
Facility Name
Saratov City Psychoneurological Dispensary
City
Saratov
ZIP/Postal Code
410038
Country
Russian Federation
Facility Name
Smolensk Regional Clinical Hospital/Children's neurological department
City
Smolensk
ZIP/Postal Code
214018
Country
Russian Federation
Facility Name
Smolensk Regional Clinical Hospital/Pediatric neurological department
City
Smolensk
ZIP/Postal Code
214018
Country
Russian Federation
Facility Name
LLC "Sunterra"
City
Stavropol
ZIP/Postal Code
355000
Country
Russian Federation
Facility Name
Stavropol Regional Clinical Specialized Psychiatric Hospital # 1/Children's department # 17
City
Stavropol
ZIP/Postal Code
355038
Country
Russian Federation
Facility Name
Regional Clinical Psychoneurological Dispensary/Outpatient clinic # 2
City
Tver
ZIP/Postal Code
170026
Country
Russian Federation
Facility Name
Children's City Clinical Hospital of Ulyanovsk city
City
Ulyanovsk
ZIP/Postal Code
432017
Country
Russian Federation
Facility Name
Yaroslavl State Medical University/Department of Polyclinic Pediatrics
City
Yaroslavl
ZIP/Postal Code
150000
Country
Russian Federation

12. IPD Sharing Statement

Learn more about this trial

Clinical Trial of Efficacy and Safety of Prospecta in the Treatment of Attention Deficit/Hyperactivity Disorder in Children

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