Phase 2 Hearing Loss Trial, Recruiting NCT07364747 Sponsor: Siriraj Hospital Condition: Hearing Loss
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Phase 2 Hearing Loss Trial, Recruiting

NCT07364747
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You are between 18 and 70 years old
  • You are planned to receive a high-dose cisplatin-based chemotherapy treatment, with a total planned dose above 200 mg/m² and each individual dose above 50 mg/m² (confirm with trial site if unsure about your dose)
  • You may also be receiving other chemotherapy drugs at the same time, as long as those drugs are not known to cause hearing damage
  • You may also be receiving radiation therapy to the base of the skull at the same time, as long as the radiation dose stays below the level that could harm hearing
  • You are taking a specific type of anti-nausea medication — either Olanzapine or a type called an NK1 receptor antagonist — as part of your treatment
  • You are receiving your medical care at Siriraj Hospital

Who may not be able to join:

  • You have been diagnosed with nasopharyngeal carcinoma (a type of cancer at the back of the nose/throat)
  • You have previously had radiation therapy to the head or neck where the dose to certain hearing-related structures (the cochlea or eustachian tube) was above specific levels (confirm with trial site)
  • You have taken a medication called N-acetylcysteine (NAC) in the 2 weeks before the study begins
  • You have taken certain medications known to cause hearing damage in the 2 weeks before or during the study — these include some antibiotics (aminoglycosides, vancomycin), water pills (such as furosemide), high-dose aspirin, or antimalarial drugs such as quinine
  • You have a known allergy or bad reaction to acetylcysteine

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 23 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Kanthong Thongyai, Master, Siriraj Hospital

Phone: 66982469575

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Siriraj Hospital
Registry
ClinicalTrials.gov
Start date
23 December 2024
Est. completion
31 December 2026

Where this trial is recruiting

🇹🇭 Thailand

Primary endpoints

- Extended high frequency audiogram - DPOAE

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov