A Phase 3 interventional study of Ramipril 2.5 MG in Persistent Developmental Stuttering, sponsored by HaEmek Medical Center, Israel. Active, not recruiting at 2 sites in Israel. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-03-13.
Sponsored by HaEmek Medical Center, Israel · Phase 3, Interventional, and Treatment
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.
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:
Stuttering evaluation
The efficacy evaluation will be performed by speech therapists. All evaluations will be will be recorded on video
Safety evaluation:
74 studies on the registry are indexed under Stuttering; 23 are open to participants now.
This study's enrollment of 10 is below the median of 44 across 57 interventional studies indexed under Stuttering.
Browse Stuttering studies →HaEmek Medical Center, Israel is the lead sponsor of 237 studies on the registry; 11 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Inclusion Criteria:
Inclusion Criteria:
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
How quickly the kidneys clear creatinine, a waste product, from the blood. A study may estimate it from a blood test with age, weight and sex (often by the Cockcroft–Gault formula), or measure it using blood and urine collected over a set time. Given in mL/min; higher is better.
Creatinine clearance (CrCl)
How quickly the kidneys clear creatinine, a waste product, from the blood. A study may estimate it from a blood test with age, weight and sex (often by the Cockcroft–Gault formula), or measure it using blood and urine collected over a set time. Given in mL/min; higher is better.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Ramipril 2.5 MG orall, daily.
Drug: Ramipril 2.5 MG
3 month of treatment with daily Ramipril 2.5 MG
changed in stuttered syllables
The difference in stuttering measures with and without treatment will be determined.
Time frame: 4 month
Plan to share: No
No publications or documents are linked to this record.
This study is active, not recruiting, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.
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Studies of the drug tested here: Ramipril
HaEmek Medical Center, Israel →