CTRI/2022/11/047797尚未招募3 期
Voice Quality after Transoral CO2-Laser Surgery versus Single Vocal Cord Irradiation for Unilateral Stage 0 & I Glottic Larynx Cancer â?? A Randomized Phase III Trial - VoiceS
the Insel Gruppe AG Universittsklinik fr Allgemeine Innere Medizin Bern Switzerland0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1. ECOG Performance status 0-1
- •2. >=18 years of age
- •3. Histopathologically confirmed, previously
- •untreated unilateral (cT1a or unilateral cTis)
- •stage 0 or I glottic larynx cancer
- •4. History and physical examination within 28 days
- •prior registrations
排除标准
- •1. Infection hampering the voice quality at the time of voice assessment
- •2. Involvement of the anterior commissure by the tumor
- •3. Previous oncologic surgery with curative intent (exception: excisional biopsies resulting in unacceptable close R0 or R1/R2 margins may be included) or radiotherapy to larynx
- •4. Synchronous or previous malignancies. Exceptions are adequately treated basal cell carcinoma or SCC of the skin, or in situ carcinoma of the cervix uteri, low-risk prostate cancer or breast with a cancer-free follow-up time of at least 3 years, or other previous malignancy with a progression-free interval of at least 5 years
- •5. Co-existing disease prejudicing survival (expected survival less than 6 months)
- •6. Active bacterial or fungal infection requiring intravenous antibiotics at the time of registration
- •7. History of any voice disorders (not related to the SCCGL) lasting longer than 3 weeks
- •8. Illness requiring hospitalization or precluding study therapy within 28 days before registration
- •9. Presence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial
研究者
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