Silence or whisper? study tests which helps vocal cords heal best after surgery
NCT ID NCT07704125
First seen Jul 15, 2026 · Last updated Jul 16, 2026 · Updated 1 time
Summary
This trial compares two approaches to voice care after surgery for benign vocal cord lesions like polyps or cysts. One group stays completely silent for five days, while the other uses soft, low-effort whispering. Both groups then receive the same voice therapy. The study measures voice quality and patient well-being at one and three months after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- absolute voice rest or hypofunctional whispering
- What this could lead to
- If soft whispering proves as effective as complete silence, patients may have a more comfortable recovery without compromising healing.
- What could go wrong
- This is a small, early-stage trial with only 16 participants, so results may not apply to everyone. Whispering might still strain the vocal cords in some cases.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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16 people
The number who actually took part.
- Started
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Feb 2025
- Finished
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May 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age 18 years or older * Diagnosis of a benign vocal fold lesion (vocal fold polyp, cyst, or Reinke's edema) * Scheduled for microlaryngeal (phonosurgery) surgery under general anesthesia * Able to complete voice assessments and comply with the assigned postoperative voice behavior protocol * Provided written informed consent Exclusion Criteria: * Malignant or premalignant vocal fold lesions * Previous laryngeal surgery or radiotherapy to the head and neck * Neurological voice disorders (e.g., vocal fold paralysis, spasmodic dysphonia) * Significant psychiatric or cognitive impairment preventing protocol compliance * Active smoking without cessation in Reinke's edema cases where required (if applicable) * Inability or unwillingness to attend follow-up assessments
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Marmara University School of Medicine, Department of Otorhinolaryngology - Head and Neck Surgery
Istanbul, Istanbul, 34854, Turkey (Türkiye)
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