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Explorative Study for Treating Persistent Developmental Stuttering With Ramipril

Primary Purpose

Persistent Developmental Stuttering

Status
Recruiting
Phase
Phase 3
Locations
Israel
Study Type
Interventional
Intervention
Ramipril 2.5 MG
Sponsored by
HaEmek Medical Center, Israel
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Persistent Developmental Stuttering

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Inclusion Criteria:

  • Age 18 or above
  • Developmental stuttering of 10 points severity at least (SSI-4)
  • Agree not to have any speech or emotional therapy during the trial.

Exclusion Criteria:

  • Systolic blood pressure < 110mmHg
  • Estimated creatinine clearance < 50ml/min
  • Baseline potassium > 5meq/ml
  • Any sign of psychopathology by the MINI international neuropsychiatric interview
  • Any psychotropic medications or substances in the past month
  • History of angioedema or cough with any ACE inhibitor
  • Aliskerin use in diabetes patients
  • Current medication include ACE inhibitors or ARBS
  • Pregnancy, or pregnancy plans during the study
  • Less than 3% stuttered syllables
  • Subjects with cluttering-stuttering when the cluttering is prominent

Sites / Locations

  • Haemek Medical CenterRecruiting
  • Asaf HaropheRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Ramipril 2.5 MG

Arm Description

Ramipril 2.5 MG orall, daily.

Outcomes

Primary Outcome Measures

changed in stuttered syllables
The difference in stuttering measures with and without treatment will be determined.

Secondary Outcome Measures

Full Information

First Posted
November 7, 2019
Last Updated
March 15, 2022
Sponsor
HaEmek Medical Center, Israel
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1. Study Identification

Unique Protocol Identification Number
NCT04173949
Brief Title
Explorative Study for Treating Persistent Developmental Stuttering With Ramipril
Official Title
Explorative Study for Treating Persistent Developmental Stuttering With Ramipril
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 15, 2020 (Actual)
Primary Completion Date
June 15, 2023 (Anticipated)
Study Completion Date
November 15, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
HaEmek Medical Center, Israel

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Persistent developmental stuttering (PDS) is diagnosed when developmental stuttering persists beyond adolescence. Most stutterers experience vast improvement in stuttering during childhood and it generally disappears within five years. A minority of stutterers continue stuttering over age 18, often accompanied by social and personal difficulties. Following a report of a 75 year old woman, with severe Persistent developmental stuttering , who experienced significant improvement in her stuttering since treated by Ramipril for hypertension, we scrutinized the literature, and discovered that there is a physiological basis for this surprising reaction. Ace inhibitors, such as Ramipril, might in fact be successful for treating Persistent developmental stuttering . In theory, it seems that ACE inhibitors, such as Ramipril could improve stuttering by reducing striatum dopamine levels. Stuttering is associated with high striatum dopamine levels Angiotensin receptors are present in the striatum Angiotensin causes elevated striatum dopamine levels ACE inhibitors penetrate the blood brain barrier and reduce brain angiotensin II levels. Methods The study will begin as a pilot study in which 10 stuttering patients will be recruited for 12 weeks on open label Ramipril 1.25mg/d. If there is improvement in at least 2 of the stuttering patients, we will continue to the main study. Efficacy Evaluation: The MINI Neuropsychiatric interview will be used to rule out major neuropsychiatric conditions Stuttering evaluation Stuttering Severity instrument Version 4 (SSI-4) (Riley 2009) SLD :Percentage of stuttered syllables (Yairi 2015) The Subjective Screening of Stuttering (SSS) Speech Situation Checklist (Brutten 1975,1981) Leibowitz Social Anxiety Scale (Leibowitz 1987) The efficacy evaluation will be performed by speech therapists. All evaluations will be will be recorded on video Safety evaluation: Blood pressure: The average of three consecutive measures. Blood pressure will be measure in both arms on the first meeting, and thereafter on the arm with the highest measurements. Orthostatic hypotension will be defined as a drop of 20mmHg systolic or 10mmHg diastolic, one and three minutes after standing from sitting position. Creatinine clearance will be calculated by the MDRD method (Levy 2006) GFR, in mL/min per 1.73 m2 = 186.3 x SCr (exp[-1.154]) x Age (exp[-0.203]) x (0.742 if female) x (1.21 if black)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Persistent Developmental Stuttering

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Model Description
The study will begin as a pilot study in which 10 stuttering patients will be recruited for 12 weeks on open label Ramipril 2.5mg.
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Ramipril 2.5 MG
Arm Type
Experimental
Arm Description
Ramipril 2.5 MG orall, daily.
Intervention Type
Drug
Intervention Name(s)
Ramipril 2.5 MG
Intervention Description
3 month of treatment with daily Ramipril 2.5 MG
Primary Outcome Measure Information:
Title
changed in stuttered syllables
Description
The difference in stuttering measures with and without treatment will be determined.
Time Frame
4 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Inclusion Criteria: Age 18 or above Developmental stuttering of 10 points severity at least (SSI-4) Agree not to have any speech or emotional therapy during the trial. Exclusion Criteria: Systolic blood pressure < 110mmHg Estimated creatinine clearance < 50ml/min Baseline potassium > 5meq/ml Any sign of psychopathology by the MINI international neuropsychiatric interview Any psychotropic medications or substances in the past month History of angioedema or cough with any ACE inhibitor Aliskerin use in diabetes patients Current medication include ACE inhibitors or ARBS Pregnancy, or pregnancy plans during the study Less than 3% stuttered syllables Subjects with cluttering-stuttering when the cluttering is prominent
Facility Information:
Facility Name
Haemek Medical Center
City
Afula
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
gilat ron avraham, mph
Phone
972-4-6495590
Email
gilat_av@clalit.org.il
First Name & Middle Initial & Last Name & Degree
Lee H Goldstein, MD
Facility Name
Asaf Harophe
City
Tzrifin
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lee Goldstein
Phone
972-4-6495590
Email
goldstein_le@clalit.org.il

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Explorative Study for Treating Persistent Developmental Stuttering With Ramipril

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