跳至主要内容
临床试验/CTRI/2024/03/063799
CTRI/2024/03/063799尚未招募Unknown

An observational study to collect and analyze volatile markers in the exhaled breath of cancer (GI, Cervical, Colorectal, head, and neck) patients using the CanScan prototype developed by Kozhnosys. - NI

Kozhnosys Private Limited0 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
Unknown
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
Observational

入排标准

入选标准

  • Inclusion Criteria for GI, Cervical, Colorectal, head, and neck Cancer
  • 1. Willing to fill out the informed consent form
  • 2. Female in the age group 20 to 80 years Women with newly diagnosed cancer (GI, Cervical, Colorectal, head, and neck) with/without common medical conditions like Hypertension, Hyperlipidaemia, Hypothyroidism, Arthritis, Asthma, GERD, Diabetes, PCOD, Vitamin deficiencies, etc. -20 evaluable subjects (4 patients each with above-mentioned cancer)
  • 3. Confirmed cases of GI, Cervical, Colorectal, head, and neck cancer but not exposed to any previous treatment cycle/surgery.
  • 4. Cases confirmed through endoscopy, PAP smear, Colonoscopy, MRI/CT, Ultrasonography or blood tests.

排除标准

  • Exclusion Criteria for GI, Cervical, Colorectal, head, and neck cancer
  • 1. The age group is below 20 years.
  • 2. Any known illness within 2 weeks from breath collection.
  • 3. Already undergoing cancer treatment.
  • 4. Undergone surgery for cancer tumor removal.
  • 5. Undergoing chemo/radiation therapy for cancer treatment.
  • 6. Positive, but no GI, Cervical, Colorectal, head, and neck cancer on the later investigation (Positive Sonography but negative biopsy report).

研究者

发起方
Kozhnosys Private Limited

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