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Effect of Aprepitant Delayed Administration on CINV and PK in DOC+DDP Chemotherapy

Effect of Aprepitant Delayed Administration on CINV and PK in DOC+DDP Chemotherapy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016704
Enrollment
Unknown
Registered
2018-06-19
Start date
2017-10-09
Completion date
Unknown
Last updated
2018-06-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nausea and vomiting caused by chemotherapy of DP regimen in cancer patients

Interventions

Case series:Aprepitant delayed administration

Sponsors

The Second Xiangya Hospital of Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 74 Years

Inclusion criteria

Inclusion criteria: (1) Adult males or females older than 18 years of age; (2) Patients diagnosed with malignant solid tumors after histopathological examination; (3) No medical treatment after diagnosis (chemotherapy, radiotherapy, molecular targeting, immunization) Etc.); (4) can accept high emetogenic DP regimen chemotherapy (docetaxel 75mg/m2 d1 + cisplatin 25mg/m2 d1-3), and before and after the two cycles of chemotherapy drug dose and adjuvant drugs are the same;; (5) No diabetes, peptic ulcer, no serious organ failure and immune deficiency, normal blood and liver, kidney function and electrolytes; (6) No vomiting within 24 hours before chemotherapy, and no other antiemetics And sedatives; (7) No brain metastases; (8) Observing and signing informed consent forms, which can actively cooperate with treatment and blood collection.

Exclusion criteria

Exclusion criteria: (1) Nausea and vomiting have occurred within 24 hours before chemotherapy; (2) Nausea and vomiting caused by primary central nervous system malignancies, central nervous system metastases, gastrointestinal obstruction, and radiotherapy; (3) Benzodiazepines are being used. Zhuo, dexamethasone and other sedative medications

Design outcomes

Primary

MeasureTime frame
Clinical index;Blood concentration;

Countries

China

Contacts

Public ContactMa Jin-An

The Second Xiangya Hospital of Central South University

3420248369@qq.com+86 13973192715

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026